Trial Outcomes & Findings for Oral Hygiene in Assisted Living (NCT NCT03892200)
NCT ID: NCT03892200
Last Updated: 2026-04-16
Results Overview
The Plaque Index for Long-Term Care (PI-LTC) is a modification of the Simplified Oral Hygiene Index. It is derived by separately scoring the buccal and lingual surfaces of six sextants in the mouth (left, front, and right regions of the upper and lower jaw), resulting in 12 separate observations for residents with a full set of teeth; sextants not containing teeth do not receive a score. Within each sextant, the tooth surface with the worst plaque is scratched using an explorer and assigned a score (0=no plaque or stain present; 1=soft plaque covering not more than one third of the tooth surface or presence of extrinsic stains without other plaque regardless of surface area covered; 2=soft plaque covering between one third and two thirds of the tooth surface; or 3=soft plaque covering more than two thirds of the exposed tooth surface). PI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
COMPLETED
NA
1405 participants
Baseline Visit
2026-04-16
Participant Flow
For Aims 2 and 3, assisted living (AL) communities were recruited and randomized to treatment arms. Within communities, AL residents (primary participants) were recruited for observation at up to 3 timepoints (baseline, 4 months, 8 months). A total of 200+214=414 residents across 24+28=52 communities were enrolled. AL Staff (983=461+366+156) and public health dental hygienists (n=8) were also enrolled as secondary participants (not randomized and did not receive the intervention). Total = 1405.
AL residents (n=414, primary) and dental hygienists (n=8, secondary) were interviewed at baseline and 4-months. AL staff (n=983=461+366+156, secondary) completed cross-sectional surveys at up to 3 timepoints but were not followed individually. To represent these different groups, they are shown below as "periods". The study protocol also describes instrument development in Aim 1 but it does not meet the definition for a clinical trial and is not included here.
Unit of analysis: Assisted living communities
Participant milestones
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
AL Residents (Primary Participants)
STARTED
|
101 12
|
99 12
|
121 14
|
93 14
|
|
AL Residents (Primary Participants)
Plaque Index Data Provided (Baseline)
|
84 12
|
80 12
|
98 14
|
78 14
|
|
AL Residents (Primary Participants)
Gingival Index Data Provided (Baseline)
|
82 12
|
78 12
|
98 14
|
77 14
|
|
AL Residents (Primary Participants)
Denture Index Data Provided (Baseline)
|
24 12
|
19 12
|
30 14
|
16 14
|
|
AL Residents (Primary Participants)
Plaque Index Data Provided (Month 4)
|
64 12
|
59 11
|
83 13
|
69 14
|
|
AL Residents (Primary Participants)
Gingival Index Data Provided (Month 4)
|
64 12
|
59 11
|
83 13
|
69 14
|
|
AL Residents (Primary Participants)
Denture Index Data Provided (Month 4)
|
21 12
|
11 11
|
27 13
|
13 14
|
|
AL Residents (Primary Participants)
Plaque Index Data Provided (Baseline and Month 4)
|
61 12
|
56 11
|
80 13
|
66 14
|
|
AL Residents (Primary Participants)
Gingival Index Data Provided (Baseline and Month 4)
|
61 12
|
55 11
|
80 13
|
65 14
|
|
AL Residents (Primary Participants)
Denture Index Data Provided (Baseline and Month 4)
|
18 12
|
10 11
|
24 13
|
13 14
|
|
AL Residents (Primary Participants)
Plaque Index Data Provided (Month 8)
|
50 11
|
43 9
|
0 0
|
0 0
|
|
AL Residents (Primary Participants)
Gingival Index Data Provided (Month 8)
|
50 11
|
43 9
|
0 0
|
0 0
|
|
AL Residents (Primary Participants)
Denture Index Data Provided (Month 8)
|
15 11
|
9 9
|
0 0
|
0 0
|
|
AL Residents (Primary Participants)
COMPLETED
|
82 12
|
65 11
|
104 13
|
81 14
|
|
AL Residents (Primary Participants)
NOT COMPLETED
|
19 0
|
34 1
|
17 1
|
12 0
|
|
AL Staff at Baseline (Secondary)
STARTED
|
116 12
|
117 12
|
117 14
|
111 14
|
|
AL Staff at Baseline (Secondary)
COMPLETED
|
116 12
|
117 12
|
117 14
|
111 14
|
|
AL Staff at Baseline (Secondary)
NOT COMPLETED
|
0 0
|
0 0
|
0 0
|
0 0
|
|
AL Staff at 4-months (Secondary)
STARTED
|
97 12
|
82 11
|
103 13
|
84 14
|
|
AL Staff at 4-months (Secondary)
COMPLETED
|
97 12
|
82 11
|
103 13
|
84 14
|
|
AL Staff at 4-months (Secondary)
NOT COMPLETED
|
0 0
|
0 0
|
0 0
|
0 0
|
|
AL Staff at 8-months (Secondary)
STARTED
|
82 11
|
74 9
|
0 0
|
0 0
|
|
AL Staff at 8-months (Secondary)
COMPLETED
|
82 11
|
74 9
|
0 0
|
0 0
|
|
AL Staff at 8-months (Secondary)
NOT COMPLETED
|
0 0
|
0 0
|
0 0
|
0 0
|
|
Dental Hygienists (Secondary)
STARTED
|
0 0
|
0 0
|
0 0
|
8 14
|
|
Dental Hygienists (Secondary)
COMPLETED
|
0 0
|
0 0
|
0 0
|
8 14
|
|
Dental Hygienists (Secondary)
NOT COMPLETED
|
0 0
|
0 0
|
0 0
|
0 0
|
Reasons for withdrawal
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
AL Residents (Primary Participants)
Death
|
10
|
19
|
2
|
6
|
|
AL Residents (Primary Participants)
Resident discharged from AL community
|
9
|
9
|
11
|
6
|
|
AL Residents (Primary Participants)
Resident found to be ineligible after baseline
|
0
|
1
|
0
|
0
|
|
AL Residents (Primary Participants)
Assisted Living (AL) community withdrew from study
|
0
|
5
|
4
|
0
|
Baseline Characteristics
Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
Baseline characteristics by cohort
| Measure |
Standard Mouth Care-Aim2
n=12 AL Communities
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=12 AL Communities
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=14 AL Communities
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=14 AL Communities
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
Total
n=52 AL Communities
Total of all reporting groups
|
|---|---|---|---|---|---|
|
Age, Continuous
AL Residents at Baseline (Primary)
|
83.6 years
STANDARD_DEVIATION 8.9 • n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
83.8 years
STANDARD_DEVIATION 9.0 • n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
79.9 years
STANDARD_DEVIATION 10.4 • n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
82.8 years
STANDARD_DEVIATION 8.6 • n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
82.4 years
STANDARD_DEVIATION 9.5 • n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Age, Continuous
AL Staff at Baseline (Secondary)
|
41.0 years
STANDARD_DEVIATION 13.3 • n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
37.5 years
STANDARD_DEVIATION 13.6 • n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
38.5 years
STANDARD_DEVIATION 13.8 • n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
37.6 years
STANDARD_DEVIATION 14.1 • n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
39.2 years
STANDARD_DEVIATION 13.5 • n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Age, Continuous
AL Staff at 4-Months (Secondary)
|
42.9 years
STANDARD_DEVIATION 13.5 • n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
39.0 years
STANDARD_DEVIATION 13.2 • n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
38.5 years
STANDARD_DEVIATION 14.6 • n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
40.2 years
STANDARD_DEVIATION 14.7 • n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
40.2 years
STANDARD_DEVIATION 14.2 • n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Age, Continuous
AL Staff at 8-Months (Secondary)
|
41.6 years
STANDARD_DEVIATION 13.8 • n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
38.3 years
STANDARD_DEVIATION 13.0 • n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
40.0 years
STANDARD_DEVIATION 13.5 • n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Age, Continuous
Dental Hygienists at Baseline (Secondary)
|
—
|
—
|
—
|
44.3 years
STANDARD_DEVIATION 9.4 • n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
44.3 years
STANDARD_DEVIATION 9.4 • n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
AL Residents (Primary) · Female
|
71 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
71 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
83 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
69 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
294 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
AL Residents (Primary) · Male
|
28 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
24 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
36 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
22 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
110 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
AL Residents (Primary) · Not Reported
|
2 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
4 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
10 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
AL Staff at Baseline (Secondary) · Female
|
105 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
105 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
98 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
95 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
403 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
AL Staff at Baseline (Secondary) · Male
|
8 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
4 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
5 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
6 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
23 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
AL Staff at Baseline (Secondary) · Not Reported
|
3 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
8 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
14 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
10 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
35 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
AL Staff at 4-Months (Secondary) · Female
|
83 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
74 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
86 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
74 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
317 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
AL Staff at 4-Months (Secondary) · Male
|
6 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
4 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
4 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
16 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
AL Staff at 4-Months (Secondary) · Not Reported
|
8 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
6 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
13 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
6 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
33 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
AL Staff at 8-Months (Secondary) · Female
|
72 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
69 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
141 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
AL Staff at 8-Months (Secondary) · Male
|
6 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
8 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
AL Staff at 8-Months (Secondary) · Not Reported
|
4 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
3 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
7 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
Period: Dental Hygienists (Secondary) · Female
|
—
|
—
|
—
|
8 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
8 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
Period: Dental Hygienists (Secondary) · Male
|
—
|
—
|
—
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Sex/Gender, Customized
Period: Dental Hygienists (Secondary) · Not Reported
|
—
|
—
|
—
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
AL Residents (Primary) · Hispanic or Latino
|
2 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
1 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
7 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
AL Residents (Primary) · Not Hispanic or Latino
|
97 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
93 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
117 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
89 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
396 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
AL Residents (Primary) · Unknown or Not Reported
|
2 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
4 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
3 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
11 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
AL Staff at Baseline (Secondary) · Hispanic or Latino
|
3 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
5 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
12 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
6 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
26 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
AL Staff at Baseline (Secondary) · Not Hispanic or Latino
|
82 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
81 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
80 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
76 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
319 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
AL Staff at Baseline (Secondary) · Unknown or Not Reported
|
31 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
31 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
25 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
29 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
116 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
AL Staff at 4-Months (Secondary) · Hispanic or Latino
|
5 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
1 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
4 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
4 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
14 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
AL Staff at 4-Months (Secondary) · Not Hispanic or Latino
|
66 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
62 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
77 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
60 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
265 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
AL Staff at 4-Months (Secondary) · Unknown or Not Reported
|
26 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
19 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
22 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
20 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
87 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
AL Staff at 8-Months (Secondary) · Hispanic or Latino
|
6 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
6 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
AL Staff at 8-Months (Secondary) · Not Hispanic or Latino
|
50 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
59 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
109 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
AL Staff at 8-Months (Secondary) · Unknown or Not Reported
|
26 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
15 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
41 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
Dental Hygienists (Secondary) · Hispanic or Latino
|
—
|
—
|
—
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
Dental Hygienists (Secondary) · Not Hispanic or Latino
|
—
|
—
|
—
|
8 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
8 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Ethnicity (NIH/OMB)
Dental Hygienists (Secondary) · Unknown or Not Reported
|
—
|
—
|
—
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Residents (Primary) · American Indian or Alaska Native
|
0 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
1 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
1 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Residents (Primary) · Asian
|
0 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Residents (Primary) · Native Hawaiian or Other Pacific Islander
|
0 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Residents (Primary) · Black or African American
|
11 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
7 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
19 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
11 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
48 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Residents (Primary) · White
|
87 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
87 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
99 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
79 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
352 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Residents (Primary) · More than one race
|
0 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
1 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
1 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Residents (Primary) · Unknown or Not Reported
|
3 Participants
n=101 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
3 Participants
n=99 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=121 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=93 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
10 Participants
n=414 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at Baseline (Secondary) · American Indian or Alaska Native
|
5 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
4 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
11 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at Baseline (Secondary) · Asian
|
1 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
1 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
4 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
6 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at Baseline (Secondary) · Native Hawaiian or Other Pacific Islander
|
0 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
6 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
6 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at Baseline (Secondary) · Black or African American
|
66 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
51 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
39 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
49 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
205 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at Baseline (Secondary) · White
|
40 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
54 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
57 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
40 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
191 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at Baseline (Secondary) · More than one race
|
1 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
3 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
6 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
4 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
14 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at Baseline (Secondary) · Unknown or Not Reported
|
3 Participants
n=116 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
4 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
11 Participants
n=117 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
10 Participants
n=111 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
28 Participants
n=461 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 4-Months (Secondary) · American Indian or Alaska Native
|
2 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
3 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
3 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
8 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 4-Months (Secondary) · Asian
|
0 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
1 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
3 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 4-Months (Secondary) · Native Hawaiian or Other Pacific Islander
|
1 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
1 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
11 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
13 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 4-Months (Secondary) · Black or African American
|
55 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
41 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
39 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
36 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
171 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 4-Months (Secondary) · White
|
29 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
33 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
44 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
26 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
132 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 4-Months (Secondary) · More than one race
|
3 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
5 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
4 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
12 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 4-Months (Secondary) · Unknown or Not Reported
|
7 Participants
n=97 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
5 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
9 Participants
n=103 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
6 Participants
n=84 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
27 Participants
n=366 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 8-Months (Secondary) · American Indian or Alaska Native
|
1 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
1 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 8-Months (Secondary) · Asian
|
0 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
1 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
1 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 8-Months (Secondary) · Native Hawaiian or Other Pacific Islander
|
1 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
1 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 8-Months (Secondary) · Black or African American
|
36 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
36 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
72 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 8-Months (Secondary) · White
|
34 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
35 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
69 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 8-Months (Secondary) · More than one race
|
4 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
4 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
AL Staff at 8-Months (Secondary) · Unknown or Not Reported
|
6 Participants
n=82 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
2 Participants
n=74 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
—
|
—
|
8 Participants
n=156 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
Dental Hygienists (Secondary) · American Indian or Alaska Native
|
—
|
—
|
—
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
Dental Hygienists (Secondary) · Asian
|
—
|
—
|
—
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
Dental Hygienists (Secondary) · Native Hawaiian or Other Pacific Islander
|
—
|
—
|
—
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
Dental Hygienists (Secondary) · Black or African American
|
—
|
—
|
—
|
1 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
1 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
Dental Hygienists (Secondary) · White
|
—
|
—
|
—
|
7 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
7 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
Dental Hygienists (Secondary) · More than one race
|
—
|
—
|
—
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Race (NIH/OMB)
Dental Hygienists (Secondary) · Unknown or Not Reported
|
—
|
—
|
—
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
0 Participants
n=8 Participants • Rows show different study populations (not one population followed over time). AL staff (secondary) completed cross-sectional interviews at up to 3 timepoints and were not followed individually. Baseline characteristics are summarized by the number of participants surveyed at each timepoint.
|
|
Region of Enrollment
United States
|
396 Participants
n=396 Participants
|
372 Participants
n=372 Participants
|
341 Participants
n=341 Participants
|
296 Participants
n=296 Participants
|
1405 Participants
n=1405 Participants
|
PRIMARY outcome
Timeframe: Baseline VisitPopulation: This measure only applies to Aim2. All data are reported.
The Plaque Index for Long-Term Care (PI-LTC) is a modification of the Simplified Oral Hygiene Index. It is derived by separately scoring the buccal and lingual surfaces of six sextants in the mouth (left, front, and right regions of the upper and lower jaw), resulting in 12 separate observations for residents with a full set of teeth; sextants not containing teeth do not receive a score. Within each sextant, the tooth surface with the worst plaque is scratched using an explorer and assigned a score (0=no plaque or stain present; 1=soft plaque covering not more than one third of the tooth surface or presence of extrinsic stains without other plaque regardless of surface area covered; 2=soft plaque covering between one third and two thirds of the tooth surface; or 3=soft plaque covering more than two thirds of the exposed tooth surface). PI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
n=84 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=80 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Plaque Index Score for Long-Term Care (PI-LTC) - Baseline-Aim2
|
1.6 score on a scale
Standard Deviation 0.7
|
1.6 score on a scale
Standard Deviation 0.7
|
—
|
—
|
PRIMARY outcome
Timeframe: 4 Months Follow-up VisitPopulation: This measure only applies to Aim2. All data are reported.
The Plaque Index for Long-Term Care (PI-LTC) is a modification of the Simplified Oral Hygiene Index. It is derived by separately scoring the buccal and lingual surfaces of six sextants in the mouth (left, front, and right regions of the upper and lower jaw), resulting in 12 separate observations for residents with a full set of teeth; sextants not containing teeth do not receive a score. Within each sextant, the tooth surface with the worst plaque is scratched using an explorer and assigned a score (0=no plaque or stain present; 1=soft plaque covering not more than one third of the tooth surface or presence of extrinsic stains without other plaque regardless of surface area covered; 2=soft plaque covering between one third and two thirds of the tooth surface; or 3=soft plaque covering more than two thirds of the exposed tooth surface). PI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
n=64 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=59 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Plaque Index Score for Long-Term Care (PI-LTC) - 4 Months-Aim2
|
1.6 score on a scale
Standard Deviation 0.7
|
1.3 score on a scale
Standard Deviation 0.7
|
—
|
—
|
PRIMARY outcome
Timeframe: Change from Baseline to 4 monthsPopulation: This measure only applies to Aim2. All data are reported.
The Plaque Index for Long-Term Care (PI-LTC) is a modification of the Simplified Oral Hygiene Index. It is derived by separately scoring the buccal and lingual surfaces of six sextants in the mouth (left, front, and right regions of the upper and lower jaw), resulting in 12 separate observations for residents with a full set of teeth; sextants not containing teeth do not receive a score. Within each sextant, the tooth surface with the worst plaque is scratched using an explorer and assigned a score (0=no plaque or stain present; 1=soft plaque covering not more than one third of the tooth surface or presence of extrinsic stains without other plaque regardless of surface area covered; 2=soft plaque covering between one third and two thirds of the tooth surface; or 3=soft plaque covering more than two thirds of the exposed tooth surface). PI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
n=61 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=56 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Change in Plaque Index Score for Long-Term Care (PI-LTC) - 4 Months-Aim2
|
0.1 score on a scale
Standard Deviation 0.6
|
-0.3 score on a scale
Standard Deviation 0.6
|
—
|
—
|
PRIMARY outcome
Timeframe: Baseline VisitPopulation: This measure only applies to Aim2. All data are reported.
The Gingival Index for Long-Term Care (GI-LTC) is a modification of the Gingival Index. Within each sextant, the most inflamed gingival surface is identified, swept using an explorer, and assigned a score (0=no inflammation; 1=mild inflammation, slight change in color, little change in texture; 2=moderate inflammation, glazing, redness, edema, and/or hypertrophy; or 3=severe inflammation, marked redness, edema and/or hypertrophy of the marginal or papillary gingival unit, spontaneous bleeding, congestion, or ulceration). Overall GI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
n=82 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=78 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Gingival Index Score for Long-Term Care (GI-LTC) - Baseline-Aim2
|
1.8 score on a scale
Standard Deviation 0.9
|
1.7 score on a scale
Standard Deviation 0.9
|
—
|
—
|
PRIMARY outcome
Timeframe: 4 Months Follow-up VisitPopulation: This measure only applies to Aim2. All data are reported.
The Gingival Index for Long-Term Care (GI-LTC) is a modification of the Gingival Index. Within each sextant, the most inflamed gingival surface is identified, swept using an explorer, and assigned a score (0=no inflammation; 1=mild inflammation, slight change in color, little change in texture; 2=moderate inflammation, glazing, redness, edema, and/or hypertrophy; or 3=severe inflammation, marked redness, edema and/or hypertrophy of the marginal or papillary gingival unit, spontaneous bleeding, congestion, or ulceration). Overall GI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
n=64 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=59 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Gingival Index Score for Long-Term Care (GI-LTC) - 4 Months-Aim2
|
1.7 score on a scale
Standard Deviation 0.9
|
1.3 score on a scale
Standard Deviation 0.8
|
—
|
—
|
PRIMARY outcome
Timeframe: Change from Baseline to 4 MonthsPopulation: This measure only applies to Aim2. All data are reported.
The Gingival Index for Long-Term Care (GI-LTC) is a modification of the Gingival Index. Within each sextant, the most inflamed gingival surface is identified, swept using an explorer, and assigned a score (0=no inflammation; 1=mild inflammation, slight change in color, little change in texture; 2=moderate inflammation, glazing, redness, edema, and/or hypertrophy; or 3=severe inflammation, marked redness, edema and/or hypertrophy of the marginal or papillary gingival unit, spontaneous bleeding, congestion, or ulceration). Overall GI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
n=61 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=55 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Change in Gingival Index Score for Long-Term Care (GI-LTC) - 4 Months-Aim2
|
0.0 score on a scale
Standard Deviation 0.7
|
-0.3 score on a scale
Standard Deviation 0.6
|
—
|
—
|
PRIMARY outcome
Timeframe: Baseline VisitPopulation: This measure only applies to Aim2. All data are reported.
The Denture Plaque Index (DPI) is scored by removing the denture, placing it in a bath of disclosing solution for 30 seconds, rinsing it under lukewarm water for 15 seconds, and assigning a score to each of four quadrants (upper and lower, and lingual and buccal) as follows: 0=no plaque, 1=light plaque (1-25% of area covered), 2=moderate plaque (26-50% of area covered), 3=heavy plaque (51-75% of area covered), or 4=very heavy plaque (76 100% of area covered). DPI is reported as the mean score of all quadrants and lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
n=24 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=19 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Denture Plaque Index Score (DPI) - Baseline-Aim2
|
2.7 score on a scale
Standard Deviation 1.1
|
2.3 score on a scale
Standard Deviation 1.2
|
—
|
—
|
PRIMARY outcome
Timeframe: 4 Months Follow-up VisitPopulation: This measure only applies to Aim2. All data are reported.
The Denture Plaque Index (DPI) is scored by removing the denture, placing it in a bath of disclosing solution for 30 seconds, rinsing it under lukewarm water for 15 seconds, and assigning a score to each of four quadrants (upper and lower, and lingual and buccal) as follows: 0=no plaque, 1=light plaque (1-25% of area covered), 2=moderate plaque (26-50% of area covered), 3=heavy plaque (51-75% of area covered), or 4=very heavy plaque (76 100% of area covered). DPI is reported as the mean score of all quadrants and lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
n=21 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=11 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Denture Plaque Index Score (DPI) - 4 Months-Aim2
|
2.4 score on a scale
Standard Deviation 1.1
|
1.8 score on a scale
Standard Deviation 1.3
|
—
|
—
|
PRIMARY outcome
Timeframe: Change from Baseline to 4 monthsPopulation: This measure only applies to Aim2. All data are reported.
The Denture Plaque Index (DPI) is scored by removing the denture, placing it in a bath of disclosing solution for 30 seconds, rinsing it under lukewarm water for 15 seconds, and assigning a score to each of four quadrants (upper and lower, and lingual and buccal) as follows: 0=no plaque, 1=light plaque (1-25% of area covered), 2=moderate plaque (26-50% of area covered), 3=heavy plaque (51-75% of area covered), or 4=very heavy plaque (76 100% of area covered). DPI is reported as the mean score of all quadrants and lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
n=18 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=10 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Change in Denture Plaque Index Score (DPI) - 4 Months-Aim2
|
-0.2 score on a scale
Standard Deviation 1.2
|
-0.7 score on a scale
Standard Deviation 1.2
|
—
|
—
|
PRIMARY outcome
Timeframe: Baseline VisitPopulation: This measure only applies to Aim3. All data are reported.
The Plaque Index for Long-Term Care (PI-LTC) is a modification of the Simplified Oral Hygiene Index. It is derived by separately scoring the buccal and lingual surfaces of six sextants in the mouth (left, front, and right regions of the upper and lower jaw), resulting in 12 separate observations for residents with a full set of teeth; sextants not containing teeth do not receive a score. Within each sextant, the tooth surface with the worst plaque is scratched using an explorer and assigned a score (0=no plaque or stain present; 1=soft plaque covering not more than one third of the tooth surface or presence of extrinsic stains without other plaque regardless of surface area covered; 2=soft plaque covering between one third and two thirds of the tooth surface; or 3=soft plaque covering more than two thirds of the exposed tooth surface). PI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=98 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=78 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Plaque Index Score for Long-Term Care (PI-LTC) - Baseline-Aim3
|
—
|
—
|
1.5 score on a scale
Standard Deviation 0.8
|
1.7 score on a scale
Standard Deviation 0.8
|
PRIMARY outcome
Timeframe: 4 Months Follow-up VisitPopulation: This measure only applies to Aim3. All data are reported.
The Plaque Index for Long-Term Care (PI-LTC) is a modification of the Simplified Oral Hygiene Index. It is derived by separately scoring the buccal and lingual surfaces of six sextants in the mouth (left, front, and right regions of the upper and lower jaw), resulting in 12 separate observations for residents with a full set of teeth; sextants not containing teeth do not receive a score. Within each sextant, the tooth surface with the worst plaque is scratched using an explorer and assigned a score (0=no plaque or stain present; 1=soft plaque covering not more than one third of the tooth surface or presence of extrinsic stains without other plaque regardless of surface area covered; 2=soft plaque covering between one third and two thirds of the tooth surface; or 3=soft plaque covering more than two thirds of the exposed tooth surface). PI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=83 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=69 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Plaque Index Score for Long-Term Care (PI-LTC) - 4 Months-Aim3
|
—
|
—
|
1.5 score on a scale
Standard Deviation 0.7
|
1.5 score on a scale
Standard Deviation 0.7
|
PRIMARY outcome
Timeframe: Change from Baseline to 4 monthsPopulation: This measure only applies to Aim3. All data are reported.
The Plaque Index for Long-Term Care (PI-LTC) is a modification of the Simplified Oral Hygiene Index. It is derived by separately scoring the buccal and lingual surfaces of six sextants in the mouth (left, front, and right regions of the upper and lower jaw), resulting in 12 separate observations for residents with a full set of teeth; sextants not containing teeth do not receive a score. Within each sextant, the tooth surface with the worst plaque is scratched using an explorer and assigned a score (0=no plaque or stain present; 1=soft plaque covering not more than one third of the tooth surface or presence of extrinsic stains without other plaque regardless of surface area covered; 2=soft plaque covering between one third and two thirds of the tooth surface; or 3=soft plaque covering more than two thirds of the exposed tooth surface). PI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=80 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=66 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Change in Plaque Index Score for Long-Term Care (PI-LTC) - 4 Months-Aim3
|
—
|
—
|
0.0 score on a scale
Standard Deviation 0.6
|
-0.2 score on a scale
Standard Deviation 0.8
|
PRIMARY outcome
Timeframe: Baseline VisitPopulation: This measure only applies to Aim3. All data are reported.
The Gingival Index for Long-Term Care (GI-LTC) is a modification of the Gingival Index. Within each sextant, the most inflamed gingival surface is identified, swept using an explorer, and assigned a score (0=no inflammation; 1=mild inflammation, slight change in color, little change in texture; 2=moderate inflammation, glazing, redness, edema, and/or hypertrophy; or 3=severe inflammation, marked redness, edema and/or hypertrophy of the marginal or papillary gingival unit, spontaneous bleeding, congestion, or ulceration). Overall GI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=98 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=77 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Gingival Index Score for Long-Term Care (GI-LTC) - Baseline-Aim3
|
—
|
—
|
1.2 score on a scale
Standard Deviation 0.9
|
1.5 score on a scale
Standard Deviation 0.8
|
PRIMARY outcome
Timeframe: 4 Months Follow-up VisitPopulation: This measure only applies to Aim3. All data are reported.
The Gingival Index for Long-Term Care (GI-LTC) is a modification of the Gingival Index. Within each sextant, the most inflamed gingival surface is identified, swept using an explorer, and assigned a score (0=no inflammation; 1=mild inflammation, slight change in color, little change in texture; 2=moderate inflammation, glazing, redness, edema, and/or hypertrophy; or 3=severe inflammation, marked redness, edema and/or hypertrophy of the marginal or papillary gingival unit, spontaneous bleeding, congestion, or ulceration). Overall GI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=83 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=69 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Gingival Index Score for Long-Term Care (GI-LTC) - 4 Months-Aim3
|
—
|
—
|
1.2 score on a scale
Standard Deviation 0.7
|
1.2 score on a scale
Standard Deviation 0.8
|
PRIMARY outcome
Timeframe: Change from Baseline to 4 monthsPopulation: This measure only applies to Aim3. All data are reported.
The Gingival Index for Long-Term Care (GI-LTC) is a modification of the Gingival Index. Within each sextant, the most inflamed gingival surface is identified, swept using an explorer, and assigned a score (0=no inflammation; 1=mild inflammation, slight change in color, little change in texture; 2=moderate inflammation, glazing, redness, edema, and/or hypertrophy; or 3=severe inflammation, marked redness, edema and/or hypertrophy of the marginal or papillary gingival unit, spontaneous bleeding, congestion, or ulceration). Overall GI-LTC scores range from 0-3 and are the average sextant score. Lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=80 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=65 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Change in Gingival Index Score for Long-Term Care (GI-LTC) - 4 Months-Aim3
|
—
|
—
|
-0.0 score on a scale
Standard Deviation 0.7
|
-0.3 score on a scale
Standard Deviation 0.8
|
PRIMARY outcome
Timeframe: Baseline VisitPopulation: This measure only applies to Aim3. All data are reported.
The Denture Plaque Index (DPI) is scored by removing the denture, placing it in a bath of disclosing solution for 30 seconds, rinsing it under lukewarm water for 15 seconds, and assigning a score to each of four quadrants (upper and lower, and lingual and buccal) as follows: 0=no plaque, 1=light plaque (1-25% of area covered), 2=moderate plaque (26-50% of area covered), 3=heavy plaque (51-75% of area covered), or 4=very heavy plaque (76 100% of area covered). DPI is reported as the mean score of all quadrants and lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=30 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=16 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Denture Plaque Index Score (DPI) - Baseline-Aim3
|
—
|
—
|
2.7 score on a scale
Standard Deviation 1.0
|
2.4 score on a scale
Standard Deviation 0.9
|
PRIMARY outcome
Timeframe: 4 Months Follow-up visitPopulation: This measure only applies to Aim3. All data are reported.
The Denture Plaque Index (DPI) is scored by removing the denture, placing it in a bath of disclosing solution for 30 seconds, rinsing it under lukewarm water for 15 seconds, and assigning a score to each of four quadrants (upper and lower, and lingual and buccal) as follows: 0=no plaque, 1=light plaque (1-25% of area covered), 2=moderate plaque (26-50% of area covered), 3=heavy plaque (51-75% of area covered), or 4=very heavy plaque (76 100% of area covered). DPI is reported as the mean score of all quadrants and lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=27 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=13 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Denture Plaque Index Score (DPI) - 4 Months-Aim3
|
—
|
—
|
2.3 score on a scale
Standard Deviation 1.3
|
1.7 score on a scale
Standard Deviation 1.2
|
PRIMARY outcome
Timeframe: Change from Baseline to 4 monthsPopulation: This measure only applies to Aim3. All data are reported.
The Denture Plaque Index (DPI) is scored by removing the denture, placing it in a bath of disclosing solution for 30 seconds, rinsing it under lukewarm water for 15 seconds, and assigning a score to each of four quadrants (upper and lower, and lingual and buccal) as follows: 0=no plaque, 1=light plaque (1-25% of area covered), 2=moderate plaque (26-50% of area covered), 3=heavy plaque (51-75% of area covered), or 4=very heavy plaque (76 100% of area covered). DPI is reported as the mean score of all quadrants and lower scores are better.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=24 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=13 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Change in Denture Plaque Index Score (DPI) - 4 Months-Aim3
|
—
|
—
|
-0.5 score on a scale
Standard Deviation 1.0
|
-0.8 score on a scale
Standard Deviation 1.0
|
SECONDARY outcome
Timeframe: Cumulative from Baseline to Completion (up to 8 months)Population: This measure only applies to Aim2. All data are reported.
The total number of AL residents diagnosed with pneumonia.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
n=101 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=99 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Number of Participants Diagnosed With Pneumonia-Aim2
|
5 Participants
|
4 Participants
|
—
|
—
|
SECONDARY outcome
Timeframe: Cumulative from Baseline to Completion (up to 8 months)Population: This measure only applies to Aim2. All data are reported.
The total number AL residents with hospitalizations.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
n=101 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=99 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Number of Participants With Hospitalizations-Aim2
|
12 Participants
|
18 Participants
|
—
|
—
|
SECONDARY outcome
Timeframe: Cumulative from Baseline to Completion (up to 4 months)Population: This measure only applies to Aim3. All data are reported.
The total number of AL residents diagnosed with pneumonia.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=121 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=93 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Number of Participants Diagnosed With Pneumonia-Aim3
|
—
|
—
|
3 Participants
|
0 Participants
|
SECONDARY outcome
Timeframe: Cumulative from Baseline to Completion (up to 4 months)Population: This measure only applies to Aim3. All data are reported.
The total number of AL residents with hospitalizations.
Outcome measures
| Measure |
Standard Mouth Care-Aim2
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=121 Participants
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=93 Participants
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Number of Participants With Hospitalizations-Aim3
|
—
|
—
|
12 Participants
|
9 Participants
|
Adverse Events
Standard Mouth Care-Aim2
Daily Mouth Care-Aim2
Standard Mouth Care-Aim3
Daily Mouth Care-Aim3
Serious adverse events
| Measure |
Standard Mouth Care-Aim2
n=101 participants at risk
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=99 participants at risk
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=121 participants at risk
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=93 participants at risk
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Injury, poisoning and procedural complications
Fall resulting in persistent incapacity
|
3.0%
3/101 • Number of events 3 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.83%
1/121 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Respiratory, thoracic and mediastinal disorders
Respiratory Disorder resulting in persistent incapacity
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Vascular disorders
Stroke symptoms results in persistent incapacity
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Cardiac disorders
Cardiac problem resulting in hospitalization
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.83%
1/121 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.1%
1/93 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Skin and subcutaneous tissue disorders
Cellulitis resulting in hospitalization
|
2.0%
2/101 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Infections and infestations
COVID infection resulting in hospitalization
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
2.0%
2/99 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Injury, poisoning and procedural complications
Fall resulting in hospitalization
|
8.9%
9/101 • Number of events 9 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
6.1%
6/99 • Number of events 6 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.7%
2/121 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.1%
1/93 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Gastrointestinal disorders
Emergency Gall Bladder Surgery
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.1%
1/93 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
General disorders
General decline resulting in hospitalization
|
3.0%
3/101 • Number of events 3 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
4.0%
4/99 • Number of events 4 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.1%
1/93 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Gastrointestinal disorders
Gastrointestinal Bleed resulting in hospitalization
|
0.99%
1/101 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Infections and infestations
Clostridium difficile infection
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.1%
1/93 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Injury, poisoning and procedural complications
Laceration resulting in hospitalization
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Psychiatric disorders
Mental Status Change resulting in hospitalization
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
2.0%
2/99 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.83%
1/121 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Infections and infestations
Pneumonia resulting in hospitalization
|
3.0%
3/101 • Number of events 3 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
3.0%
3/99 • Number of events 3 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
2.5%
3/121 • Number of events 3 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Respiratory, thoracic and mediastinal disorders
Respiratory distress resulting in hospitalization
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
2.0%
2/99 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.1%
1/93 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Infections and infestations
Respiratory Syncytial Virus (RSV) infection resulting in hospitalization
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.1%
1/93 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Nervous system disorders
Seizure resulting in hospitalization
|
0.99%
1/101 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Vascular disorders
Stroke symptoms resulting in hospitalization
|
0.99%
1/101 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.1%
1/93 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Infections and infestations
Urinary tract infection resulting in hospitalization
|
0.99%
1/101 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
3.0%
3/99 • Number of events 4 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
4.1%
5/121 • Number of events 6 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.1%
1/93 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Cancer diagnosis resulting in hospitalization
|
0.99%
1/101 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Vascular disorders
Edema resulting in hospitalization
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.83%
1/121 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
General disorders
Syncope resulting in hospitalization
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
Other adverse events
| Measure |
Standard Mouth Care-Aim2
n=101 participants at risk
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim2
n=99 participants at risk
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim2 the intervention training is delivered by a research dental hygienist.
Aim2 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim2 the intervention training is delivered by a research dental hygienist.
|
Standard Mouth Care-Aim3
n=121 participants at risk
Assisted living communities will continue to provide standard mouth care to all residents. Assisted living staff will not receive training or supplies in the control condition.
|
Daily Mouth Care-Aim3
n=93 participants at risk
The intervention being tested is a standardized educational and skill-building program for use in assisted living communities, which highlights that mouth care is infection control (e.g., can reduce pneumonia); includes techniques and products to clean and protect the teeth, tongue, gums, and dentures (e.g., the jiggle-sweep approach to remove plaque, use of an interdental brush instead of floss); provides strategies for care provision in special situations (e.g., broken teeth); and includes a toolkit of dementia-sensitive approaches for people who are resistant (e.g., refuse to open the mouth). It also includes information about potential dental emergencies and issues that merit assessment.
For Aim3 the intervention training is delivered by state public health dental hygienists.
Aim3 - Daily Mouth Care: Nursing assistants will be trained to provide daily mouth care to all residents in nursing homes. Mouth care supplies will also be provided to intervention assisted living communities.
For Aim3 the intervention training is delivered by state public health dental hygienists.
|
|---|---|---|---|---|
|
Immune system disorders
Allergy to Antibiotic
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Infections and infestations
COVID infection
|
5.0%
5/101 • Number of events 5 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
19.2%
19/99 • Number of events 19 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
9.9%
12/121 • Number of events 12 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
General disorders
Syncope
|
3.0%
3/101 • Number of events 3 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.1%
1/93 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Injury, poisoning and procedural complications
Fall resulting in emergency department visit
|
7.9%
8/101 • Number of events 8 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
9.1%
9/99 • Number of events 11 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
3.3%
4/121 • Number of events 6 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Injury, poisoning and procedural complications
Fall with injury
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Infections and infestations
Gastrointestinal infection
|
5.0%
5/101 • Number of events 5 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.1%
1/93 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
General disorders
General decline
|
0.99%
1/101 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
2.0%
2/99 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Gastrointestinal disorders
Hernia
|
0.99%
1/101 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Infections and infestations
Influenza
|
2.0%
2/101 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Injury, poisoning and procedural complications
Laceration
|
0.99%
1/101 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.83%
1/121 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Psychiatric disorders
Mental status change
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.7%
2/121 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Immune system disorders
Allergic reaction in mouth
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
2.0%
2/99 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Gastrointestinal disorders
Sore in mouth
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Gastrointestinal disorders
Tooth abscess
|
0.99%
1/101 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Infections and infestations
Pneumonia
|
2.0%
2/101 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Infections and infestations
Respiratory infection
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.7%
2/121 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Nervous system disorders
Seizure
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Skin and subcutaneous tissue disorders
Shingles
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.83%
1/121 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Respiratory, thoracic and mediastinal disorders
Shortness of Breath
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.0%
1/99 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Gastrointestinal disorders
Swallowing problem
|
2.0%
2/101 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/121 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
Infections and infestations
Urinary tract infection
|
0.99%
1/101 • Number of events 1 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
4.0%
4/99 • Number of events 4 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
2.5%
3/121 • Number of events 5 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
2.2%
2/93 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
|
General disorders
General distress
|
0.00%
0/101 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/99 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
1.7%
2/121 • Number of events 2 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
0.00%
0/93 • Collected for n=414 primary participants from the time of baseline data collection until the end of study participation; for Aim 2 participants up to 8 months, for Aim 3 participants up to 4 months.
All-Cause Mortality, Serious and Other (Not including serious) adverse events were collected for assisted living residents (n=414, primary participants). All-Cause Mortality, Serious and Other (Not including serious) adverse events were NOT assessed, monitored, or collected for AL staff or dental hygienists (n=8+461+366+156 secondary, participants) because they were not randomized and did not receive the intervention.
|
Additional Information
Lynne Sampson, PhD, MPH
University of North Carolina at Chapel Hill
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place