Trial Outcomes & Findings for Social Work Intervention Focused on Transitions (NCT NCT02232126)

NCT ID: NCT02232126

Last Updated: 2023-11-09

Results Overview

The outcome measure is the number of readmissions experienced by participants in the Usual Care and Intervention groups within 30-days of their index discharge.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

181 participants

Primary outcome timeframe

30-days post hospitalization

Results posted on

2023-11-09

Participant Flow

Participant milestones

Participant milestones
Measure
Usual Care
Intervention
SWIFT home intervention: 1 in-home assessment performed by study social worker, another in-home visit performed if needed. Up to 4 telephone contacts performed by study social worker. A maximum of 6 contacts
Overall Study
STARTED
91
90
Overall Study
COMPLETED
91
90
Overall Study
NOT COMPLETED
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Social Work Intervention Focused on Transitions

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Usual Care
n=91 Participants
Usual care consisted of the usual course of care provided to older adults transitioning home from a hospital stay at Huntington Memorial Hospital
Intervention
n=90 Participants
SWIFT home intervention: 1 in-home assessment performed by study social worker, another in-home visit performed if needed. Up to 4 telephone contacts performed by study social worker. A maximum of 6 contacts
Total
n=181 Participants
Total of all reporting groups
Age, Categorical
<=18 years
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Age, Categorical
Between 18 and 65 years
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Age, Categorical
>=65 years
91 Participants
n=99 Participants
90 Participants
n=107 Participants
181 Participants
n=206 Participants
Age, Continuous
79.2 years
STANDARD_DEVIATION 8.8 • n=99 Participants
78.4 years
STANDARD_DEVIATION 7.8 • n=107 Participants
78.8 years
STANDARD_DEVIATION 8.3 • n=206 Participants
Sex: Female, Male
Female
49 Participants
n=99 Participants
39 Participants
n=107 Participants
88 Participants
n=206 Participants
Sex: Female, Male
Male
42 Participants
n=99 Participants
51 Participants
n=107 Participants
93 Participants
n=206 Participants
Race/Ethnicity, Customized
African American
23 participants
n=99 Participants
14 participants
n=107 Participants
37 participants
n=206 Participants
Race/Ethnicity, Customized
Caucasian
52 participants
n=99 Participants
57 participants
n=107 Participants
109 participants
n=206 Participants
Race/Ethnicity, Customized
Latino
7 participants
n=99 Participants
9 participants
n=107 Participants
16 participants
n=206 Participants
Race/Ethnicity, Customized
Native American
1 participants
n=99 Participants
1 participants
n=107 Participants
2 participants
n=206 Participants
Race/Ethnicity, Customized
Asian/Pacific Islander
4 participants
n=99 Participants
2 participants
n=107 Participants
6 participants
n=206 Participants
Race/Ethnicity, Customized
Other
3 participants
n=99 Participants
6 participants
n=107 Participants
9 participants
n=206 Participants
Race/Ethnicity, Customized
Declined to provide response
1 participants
n=99 Participants
1 participants
n=107 Participants
2 participants
n=206 Participants
Region of Enrollment
United States
91 participants
n=99 Participants
90 participants
n=107 Participants
181 participants
n=206 Participants
Marital status
Married
35 participants
n=99 Participants
45 participants
n=107 Participants
80 participants
n=206 Participants
Marital status
Single
11 participants
n=99 Participants
16 participants
n=107 Participants
27 participants
n=206 Participants
Marital status
Divorced
10 participants
n=99 Participants
7 participants
n=107 Participants
17 participants
n=206 Participants
Marital status
Widowed
35 participants
n=99 Participants
19 participants
n=107 Participants
54 participants
n=206 Participants
Marital status
Declined to provide response
0 participants
n=99 Participants
3 participants
n=107 Participants
3 participants
n=206 Participants
Current living situation
Own house/apartment
82 participants
n=99 Participants
78 participants
n=107 Participants
160 participants
n=206 Participants
Current living situation
Living in family member's home
7 participants
n=99 Participants
6 participants
n=107 Participants
13 participants
n=206 Participants
Current living situation
Other
2 participants
n=99 Participants
3 participants
n=107 Participants
5 participants
n=206 Participants
Current living situation
Declined to provide response
0 participants
n=99 Participants
3 participants
n=107 Participants
3 participants
n=206 Participants
Who do you live with?
Alone
35 participants
n=99 Participants
20 participants
n=107 Participants
55 participants
n=206 Participants
Who do you live with?
Spouse/partner
31 participants
n=99 Participants
43 participants
n=107 Participants
74 participants
n=206 Participants
Who do you live with?
Child
14 participants
n=99 Participants
13 participants
n=107 Participants
27 participants
n=206 Participants
Who do you live with?
Paid caregiver
2 participants
n=99 Participants
1 participants
n=107 Participants
3 participants
n=206 Participants
Who do you live with?
Other
9 participants
n=99 Participants
8 participants
n=107 Participants
17 participants
n=206 Participants
Who do you live with?
Declined to provide response
0 participants
n=99 Participants
5 participants
n=107 Participants
5 participants
n=206 Participants
Who is your primary caregiver?
No one/self
43 participants
n=99 Participants
33 participants
n=107 Participants
76 participants
n=206 Participants
Who is your primary caregiver?
Spouse
19 participants
n=99 Participants
24 participants
n=107 Participants
43 participants
n=206 Participants
Who is your primary caregiver?
Significant other
0 participants
n=99 Participants
4 participants
n=107 Participants
4 participants
n=206 Participants
Who is your primary caregiver?
Child
11 participants
n=99 Participants
11 participants
n=107 Participants
22 participants
n=206 Participants
Who is your primary caregiver?
Paid caregiver
9 participants
n=99 Participants
6 participants
n=107 Participants
15 participants
n=206 Participants
Who is your primary caregiver?
Other
9 participants
n=99 Participants
8 participants
n=107 Participants
17 participants
n=206 Participants
Who is your primary caregiver?
Declined to provide response
0 participants
n=99 Participants
4 participants
n=107 Participants
4 participants
n=206 Participants
Current annual income
Under $10,000
15 participants
n=99 Participants
9 participants
n=107 Participants
24 participants
n=206 Participants
Current annual income
$10,000-$19,000
9 participants
n=99 Participants
10 participants
n=107 Participants
19 participants
n=206 Participants
Current annual income
$20,000-$29,000
9 participants
n=99 Participants
5 participants
n=107 Participants
14 participants
n=206 Participants
Current annual income
$30,000-$39,000
3 participants
n=99 Participants
1 participants
n=107 Participants
4 participants
n=206 Participants
Current annual income
$40,000-$49,000
0 participants
n=99 Participants
1 participants
n=107 Participants
1 participants
n=206 Participants
Current annual income
$50,000 or more
11 participants
n=99 Participants
11 participants
n=107 Participants
22 participants
n=206 Participants
Current annual income
Refused to respond
44 participants
n=99 Participants
53 participants
n=107 Participants
97 participants
n=206 Participants
Highest grade completed in school
8th grade or less
1 participants
n=99 Participants
5 participants
n=107 Participants
6 participants
n=206 Participants
Highest grade completed in school
9th-11th grade
4 participants
n=99 Participants
5 participants
n=107 Participants
9 participants
n=206 Participants
Highest grade completed in school
High school graduate
17 participants
n=99 Participants
13 participants
n=107 Participants
30 participants
n=206 Participants
Highest grade completed in school
Some college
27 participants
n=99 Participants
20 participants
n=107 Participants
47 participants
n=206 Participants
Highest grade completed in school
College graduate
17 participants
n=99 Participants
19 participants
n=107 Participants
36 participants
n=206 Participants
Highest grade completed in school
Graduate degree
10 participants
n=99 Participants
14 participants
n=107 Participants
24 participants
n=206 Participants
Highest grade completed in school
Doctoral degree
7 participants
n=99 Participants
4 participants
n=107 Participants
11 participants
n=206 Participants
Highest grade completed in school
Declined to provide response
8 participants
n=99 Participants
10 participants
n=107 Participants
18 participants
n=206 Participants
Chronic condition inventory
Cancer
24 participants
n=99 Participants
20 participants
n=107 Participants
44 participants
n=206 Participants
Chronic condition inventory
Cardiac disease
58 participants
n=99 Participants
55 participants
n=107 Participants
113 participants
n=206 Participants
Chronic condition inventory
Dementia/Alzheimer's disease
3 participants
n=99 Participants
4 participants
n=107 Participants
7 participants
n=206 Participants
Chronic condition inventory
Depression
14 participants
n=99 Participants
32 participants
n=107 Participants
46 participants
n=206 Participants
Chronic condition inventory
Diabetes
18 participants
n=99 Participants
23 participants
n=107 Participants
41 participants
n=206 Participants
Chronic condition inventory
Hypertension
57 participants
n=99 Participants
54 participants
n=107 Participants
111 participants
n=206 Participants
Chronic condition inventory
Respiratory disease
30 participants
n=99 Participants
29 participants
n=107 Participants
59 participants
n=206 Participants
Chronic condition inventory
Stroke
7 participants
n=99 Participants
10 participants
n=107 Participants
17 participants
n=206 Participants
Patient Health Questionnaire 9-item (PHQ-9)
4.33 units on a scale
STANDARD_DEVIATION 3.9 • n=99 Participants
6.15 units on a scale
STANDARD_DEVIATION 5.1 • n=107 Participants
5.24 units on a scale
STANDARD_DEVIATION 4.5 • n=206 Participants
Pain (Number Rating Scale)
3.54 units on a scale
STANDARD_DEVIATION 3.4 • n=99 Participants
9.18 units on a scale
STANDARD_DEVIATION 1.1 • n=107 Participants
6.36 units on a scale
STANDARD_DEVIATION 2.25 • n=206 Participants
Physical Functioning Index (abbreviated Short Form-12)
7.67 units on a scale
STANDARD_DEVIATION 5.12 • n=99 Participants
7.18 units on a scale
STANDARD_DEVIATION 5.08 • n=107 Participants
7.43 units on a scale
STANDARD_DEVIATION 5.1 • n=206 Participants
Cognition (SPMSQ score)
9.08 units on a scale
STANDARD_DEVIATION 1.2 • n=99 Participants
9.18 units on a scale
STANDARD_DEVIATION 1.1 • n=107 Participants
9.13 units on a scale
STANDARD_DEVIATION 1.15 • n=206 Participants
Number of health conditions
6.35 health conditions
STANDARD_DEVIATION 4.1 • n=99 Participants
5.88 health conditions
STANDARD_DEVIATION 2.9 • n=107 Participants
6.17 health conditions
STANDARD_DEVIATION 3.5 • n=206 Participants
Number of daily medications
7.61 medications
STANDARD_DEVIATION 3.8 • n=99 Participants
8.00 medications
STANDARD_DEVIATION 3.8 • n=107 Participants
7.81 medications
STANDARD_DEVIATION 3.8 • n=206 Participants
Discharged home under self-care
Yes
61 participants
n=99 Participants
67 participants
n=107 Participants
128 participants
n=206 Participants
Discharged home under self-care
No
30 participants
n=99 Participants
23 participants
n=107 Participants
53 participants
n=206 Participants
Had inpatient stay or emergency department visit in previous 6 months
Yes
35 participants
n=99 Participants
32 participants
n=107 Participants
67 participants
n=206 Participants
Had inpatient stay or emergency department visit in previous 6 months
No
56 participants
n=99 Participants
58 participants
n=107 Participants
114 participants
n=206 Participants
Has Advance Directive
Yes
50 participants
n=99 Participants
46 participants
n=107 Participants
96 participants
n=206 Participants
Has Advance Directive
No
41 participants
n=99 Participants
44 participants
n=107 Participants
85 participants
n=206 Participants

PRIMARY outcome

Timeframe: 30-days post hospitalization

The outcome measure is the number of readmissions experienced by participants in the Usual Care and Intervention groups within 30-days of their index discharge.

Outcome measures

Outcome measures
Measure
Usual Care
n=91 Participants
Usual Care in the present study constitutes usual care that is delivered to older adults transitioning from the hospital to home from Huntington Memorial Hospital.
Intervention
n=90 Participants
SWIFT home intervention: 1 in-home assessment performed by study social worker, another in-home visit performed if needed. Up to 4 telephone contacts performed by study social worker. A maximum of 6 contacts
30-day Hospital Readmission
11 30-day hospital readmissions
9 30-day hospital readmissions

SECONDARY outcome

Timeframe: 30-days

Population: Analysis among Intervention group ONLY for this outcome

The outcome measure is the rate of 30-day readmissions among Intervention group participants that declined to receive the in-home social work intervention versus those Intervention group participants that received the in-home social work intervention.

Outcome measures

Outcome measures
Measure
Usual Care
n=63 Participants
Usual Care in the present study constitutes usual care that is delivered to older adults transitioning from the hospital to home from Huntington Memorial Hospital.
Intervention
n=27 Participants
SWIFT home intervention: 1 in-home assessment performed by study social worker, another in-home visit performed if needed. Up to 4 telephone contacts performed by study social worker. A maximum of 6 contacts
30-day Readmission Among Intervention Participants
4 30-day hospital readmissions
5 30-day hospital readmissions

Adverse Events

Usual Care

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Intervention

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Dr. Susan Enguidanos

University of Southern California

Phone: 213-740-9822

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place