Trial Outcomes & Findings for Oregon Military Employee Sleep and Health Study (NCT NCT02946736)
NCT ID: NCT02946736
Last Updated: 2025-01-03
Results Overview
Total number of hours calculated from reported bed time and wake time. Minimum 0 hours, Maximum 24 hours. Longer duration indicates longer sleep duration. Ideal range is 7-9 hours of sleep per night.
COMPLETED
NA
704 participants
4 months
2025-01-03
Participant Flow
n=215 were identified as supervisors in the intervention condition and were excluded (i.e., focus is on service members only for analysis)
Participant milestones
| Measure |
Intervention Combined: Service Member/Employees
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/Family Supportive training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
Service members do not receive actigraphy feedback nor do their supervisors receive the sleep leadership/Family Supportive training until AFTER final data collection at 9 months
|
|---|---|---|
|
Employees: 4 Month Completion
STARTED
|
358
|
346
|
|
Employees: 4 Month Completion
COMPLETED
|
295
|
289
|
|
Employees: 4 Month Completion
NOT COMPLETED
|
63
|
57
|
|
Employees: 9 Month Completion
STARTED
|
295
|
289
|
|
Employees: 9 Month Completion
COMPLETED
|
275
|
274
|
|
Employees: 9 Month Completion
NOT COMPLETED
|
20
|
15
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Missing data
Baseline characteristics by cohort
| Measure |
Intervention Combined: Service Member/Employees
n=358 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=346 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
Total
n=704 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Continuous
|
35.94 years
STANDARD_DEVIATION 8.98 • n=358 Participants
|
36.49 years
STANDARD_DEVIATION 9.18 • n=346 Participants
|
36.21 years
STANDARD_DEVIATION 9.08 • n=704 Participants
|
|
Sex: Female, Male
Female
|
90 Participants
n=357 Participants • Missing data
|
87 Participants
n=346 Participants • Missing data
|
177 Participants
n=703 Participants • Missing data
|
|
Sex: Female, Male
Male
|
267 Participants
n=357 Participants • Missing data
|
259 Participants
n=346 Participants • Missing data
|
526 Participants
n=703 Participants • Missing data
|
|
Race/Ethnicity, Customized
Dichotomized Race/Ethnicity · White
|
289 Participants
n=356 Participants • Missing data
|
276 Participants
n=344 Participants • Missing data
|
565 Participants
n=700 Participants • Missing data
|
|
Race/Ethnicity, Customized
Dichotomized Race/Ethnicity · Non-White/Multiple
|
67 Participants
n=356 Participants • Missing data
|
68 Participants
n=344 Participants • Missing data
|
135 Participants
n=700 Participants • Missing data
|
|
Region of Enrollment
United States
|
358 participants
n=358 Participants
|
346 participants
n=346 Participants
|
704 participants
n=704 Participants
|
|
Self-Reported Sleep Duration
|
7.29 Hours
STANDARD_DEVIATION 1.09 • n=358 Participants
|
7.28 Hours
STANDARD_DEVIATION 1.06 • n=346 Participants
|
7.28 Hours
STANDARD_DEVIATION 1.08 • n=704 Participants
|
|
Patient Reported Outcomes Measurement Information System (PROMIS): Sleep Disturbance Insomnia Subsca
|
52.47 units on a scale
STANDARD_DEVIATION 8.52 • n=358 Participants
|
52.79 units on a scale
STANDARD_DEVIATION 7.86 • n=346 Participants
|
52.63 units on a scale
STANDARD_DEVIATION 8.20 • n=704 Participants
|
|
Patient Reported Outcomes Measurement Information System (PROMIS): Dissatisfaction With Sleep Subsca
|
53.88 units on a scale
STANDARD_DEVIATION 7.68 • n=358 Participants
|
54.08 units on a scale
STANDARD_DEVIATION 7.33 • n=346 Participants
|
53.98 units on a scale
STANDARD_DEVIATION 7.51 • n=704 Participants
|
|
Patient Reported Outcomes Measurement Information System (PROMIS): Sleep Related Impairment Subscale
|
53.07 units on a scale
STANDARD_DEVIATION 8.85 • n=358 Participants
|
53.35 units on a scale
STANDARD_DEVIATION 8.40 • n=346 Participants
|
53.21 units on a scale
STANDARD_DEVIATION 8.63 • n=704 Participants
|
|
Actigraphic Sleep Duration: Total Sleep Time (TST)
|
6.61 Hours
STANDARD_DEVIATION .77 • n=358 Participants
|
6.59 Hours
STANDARD_DEVIATION .80 • n=346 Participants
|
6.60 Hours
STANDARD_DEVIATION .79 • n=704 Participants
|
|
Actigraphic Sleep Efficiency: Wake After Sleep Onset (WASO)
|
41.06 Minutes
STANDARD_DEVIATION 12.03 • n=358 Participants
|
41.31 Minutes
STANDARD_DEVIATION 12.81 • n=346 Participants
|
41.19 Minutes
STANDARD_DEVIATION 12.42 • n=704 Participants
|
|
Overall Job Satisfaction Scale
|
3.98 units on a scale
STANDARD_DEVIATION .85 • n=358 Participants
|
3.90 units on a scale
STANDARD_DEVIATION .85 • n=346 Participants
|
3.94 units on a scale
STANDARD_DEVIATION .85 • n=704 Participants
|
|
Turnover Intentions
|
2.04 units on a scale
STANDARD_DEVIATION 1.15 • n=358 Participants
|
2.23 units on a scale
STANDARD_DEVIATION 1.23 • n=346 Participants
|
2.13 units on a scale
STANDARD_DEVIATION 1.19 • n=704 Participants
|
|
Perceived Stress Scale
|
1.37 units on a scale
STANDARD_DEVIATION .70 • n=358 Participants
|
1.37 units on a scale
STANDARD_DEVIATION .67 • n=346 Participants
|
1.37 units on a scale
STANDARD_DEVIATION .68 • n=704 Participants
|
|
Walter Reed Functional Impairment: Occupational Subscale (OFI)
|
1.83 units on a scale
STANDARD_DEVIATION .82 • n=358 Participants
|
1.79 units on a scale
STANDARD_DEVIATION .73 • n=346 Participants
|
1.81 units on a scale
STANDARD_DEVIATION .78 • n=704 Participants
|
|
Walter Reed Functional Impairment: Social Functional Impairment (SFI)
|
1.68 units on a scale
STANDARD_DEVIATION .66 • n=358 Participants
|
1.69 units on a scale
STANDARD_DEVIATION .67 • n=346 Participants
|
1.68 units on a scale
STANDARD_DEVIATION .66 • n=704 Participants
|
|
Walter Reed Functional Impairment: Personal Functional Impairment (PFI)
|
1.60 units on a scale
STANDARD_DEVIATION .75 • n=358 Participants
|
1.63 units on a scale
STANDARD_DEVIATION .76 • n=346 Participants
|
1.61 units on a scale
STANDARD_DEVIATION .76 • n=704 Participants
|
PRIMARY outcome
Timeframe: 4 monthsTotal number of hours calculated from reported bed time and wake time. Minimum 0 hours, Maximum 24 hours. Longer duration indicates longer sleep duration. Ideal range is 7-9 hours of sleep per night.
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=270 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=271 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Self-Reported Sleep Duration
|
7.43 Hours
Standard Deviation 1.10
|
7.34 Hours
Standard Deviation 1.13
|
PRIMARY outcome
Timeframe: 9 monthsTotal number of hours calculated from reported bed time and wake time. Minimum 0 hours, Maximum 24 hours. Longer duration indicates longer sleep duration. Ideal range is 7-9 hours of sleep per night.
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=251 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=260 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Self-Reported Sleep Duration
|
7.50 Hours
Standard Deviation 1.15
|
7.39 Hours
Standard Deviation 1.21
|
PRIMARY outcome
Timeframe: 4 monthsFour item subscale of the larger 8 item Sleep Disturbance scale. Likert-type responses: 1 = Not at all to 5 = Very much). T-Scores were created using HealthMeasures Scoring service, where data are uploaded into the HealthMeasures scoring service website, which generates T-Scores. This is considered the most accurate option. T-Scores estimates were developed using a population of 2,252 participants, 259 of which had clinical sleep disorders, and was intended to be representative of the US population. This is the reference population that the T-score means and SDs were calibrated and centered with. The T-Scores that HealthMeasures generates are not precisely at a mean of 50 and standard deviation of 10 because they are based on the unique MESH samples. A higher PROMIS T-score represents more of the concept being measured (worse).
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=269 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=272 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Patient Reported Outcomes Measurement Information System (PROMIS): Sleep Disturbance Insomnia Subscale
|
50.90 t score on a scale
Standard Deviation 8.65
|
51.78 t score on a scale
Standard Deviation 8.01
|
PRIMARY outcome
Timeframe: 9 monthsFour item subscale of the larger 8 item Sleep Disturbance scale. Likert-type responses: 1 = Not at all to 5 = Very much). T-Scores were created using HealthMeasures Scoring service, where data are uploaded into the HealthMeasures scoring service website, which generates T-Scores. This is considered the most accurate option. T-Scores estimates were developed using a population of 2,252 participants, 259 of which had clinical sleep disorders, and was intended to be representative of the US population. This is the reference population that the T-score means and SDs were calibrated and centered with. The T-Scores that HealthMeasures generates are not precisely at a mean of 50 and standard deviation of 10 because they are based on the unique MESH samples. A higher PROMIS T-score represents more of the concept being measured.
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=251 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=260 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Patient Reported Outcomes Measurement Information System (PROMIS): Sleep Disturbance Insomnia Subscale
|
51.63 t score on a scale
Standard Deviation 8.48
|
52.00 t score on a scale
Standard Deviation 8.21
|
PRIMARY outcome
Timeframe: 4 monthsFour item subscale of the larger 8 item Sleep Disturbance scale. Likert-type responses: 1 = Not at all to 5 = Very much. T-Scores were created using HealthMeasures Scoring service, where data are uploaded into the HealthMeasures scoring service website, which generates T-Scores. This is considered the most accurate option. T-Scores estimates were developed using a population of 2,252 participants, 259 of which had clinical sleep disorders, and was intended to be representative of the US population. This is the reference population that the T-score means and SDs were calibrated and centered with. The T-Scores that HealthMeasures generates are not precisely at a mean of 50 and standard deviation of 10 because they are based on the unique MESH samples. A higher PROMIS T-score represents more of the concept being measured (worse).
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=269 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=272 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Patient Reported Outcomes Measurement Information System (PROMIS): Dissatisfaction With Sleep Subscale
|
52.28 t score on a scale
Standard Deviation 8.06
|
53.27 t score on a scale
Standard Deviation 7.98
|
PRIMARY outcome
Timeframe: 9 monthsFour item subscale of the larger 8 item Sleep Disturbance scale. Likert-type responses: 1 = Not at all to 5 = Very much). T-Scores were created using HealthMeasures Scoring service, where data are uploaded into the HealthMeasures scoring service website, which generates T-Scores. This is considered the most accurate option. T-Scores estimates for Dissatisfaction with Sleep were developed using a population of 2,252 participants, 259 of which had clinical sleep disorders, and was intended to be representative of the US population. This is the reference population that the T-score means and SDs were calibrated and centered with. The T-Scores that HealthMeasures generates are not precisely at a mean of 50 and standard deviation of 10 because they are based on the unique MESH samples. A higher PROMIS T-score represents more of the concept being measured (worse).
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=251 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=259 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Patient Reported Outcomes Measurement Information System (PROMIS): Dissatisfaction With Sleep Subscale
|
52.26 t score on a scale
Standard Deviation 7.79
|
53.32 t score on a scale
Standard Deviation 7.68
|
PRIMARY outcome
Timeframe: 4 months8 item scale. Likert-type responses: 1 = Not at all to 5 = Very much). T-Scores were created using HealthMeasures Scoring service, where data are uploaded into the HealthMeasures scoring service website, which generates T-Scores. This is considered the most accurate option. T-Scores estimates for SRI were developed using a population of 2,252 participants, 259 of which had clinical sleep disorders, and was intended to be representative of the US population. This is the reference population that the T-score means and SDs were calibrated and centered with. The T-Scores that HealthMeasures generates are not precisely at a mean of 50 and standard deviation of 10 because they are based on the unique MESH samples. A higher PROMIS T-score represents more sleep impairment (worse).
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=270 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=272 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Patient Reported Outcomes Measurement Information System (PROMIS): Sleep Related Impairment Subscale (SRI)
|
51.10 t score on a scale
Standard Deviation 9.58
|
52.33 t score on a scale
Standard Deviation 8.66
|
PRIMARY outcome
Timeframe: 9 months8 item scale. Likert-type responses: 1 = Not at all to 5 = Very much). T-Scores were created using HealthMeasures Scoring service, where data are uploaded into the HealthMeasures scoring service website, which generates T-Scores. This is considered the most accurate option. T-Scores estimates for SRI were developed using a population of 2,252 participants, 259 of which had clinical sleep disorders, and was intended to be representative of the US population. This is the reference population that the T-score means and SDs were calibrated and centered with. The T-Scores that HealthMeasures generates are not precisely at a mean of 50 and standard deviation of 10 because they are based on the unique MESH samples. A higher PROMIS T-score represents more sleep impairment (worse).
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=251 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=260 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Patient Reported Outcomes Measurement Information System (PROMIS): Sleep Related Impairment Subscale (SRI)
|
50.91 t score on a scale
Standard Deviation 9.12
|
51.91 t score on a scale
Standard Deviation 8.33
|
PRIMARY outcome
Timeframe: 9 monthsActigraphic measurements obtained using Actiwatch2 worn for 3 weeks Average sleep duration in hours Great duration generally better, with target range of 7-9 hours each sleep period.
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=227 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=256 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Actigraphic Sleep Duration: Total Sleep Time (TST)
|
6.65 Hours
Standard Deviation .79
|
6.54 Hours
Standard Deviation .96
|
PRIMARY outcome
Timeframe: 9-monthsActigraphic measurements obtained using Actiwatch2 worn for 3 weeks Average number of minutes spent awake during the sleep period. More minutes indicates worse outcome.
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=227 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=253 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Actigraphic Sleep Efficiency: Wake After Sleep Onset (WASO)
|
42.76 Minutes
Standard Deviation 13.90
|
42.71 Minutes
Standard Deviation 13.73
|
PRIMARY outcome
Timeframe: 9-monthsService member satisfaction with current job; Likert-type scale 1 = Strongly disagree to 5 = Strongly agree, mean created from the 3 items. Scores could range from 0-5 with higher levels indicating greater satisfaction. Source: Cammann et al., 1983
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=261 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=262 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Overall Job Satisfaction Scale
|
3.86 score on a scale
Standard Deviation .82
|
3.80 score on a scale
Standard Deviation .94
|
PRIMARY outcome
Timeframe: 9-monthsService member intention to quit current job; Two items with responses on Likert-type scale 1 = Strongly disagree to 5 = Strongly agree. Overall score created with a mean of the two items, with higher levels indicating greater intention to leave one's job. Source: Boroff \& Lewin, 1997
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=259 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=263 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Turnover Intentions
|
2.25 score on a scale
Standard Deviation 1.00
|
2.32 score on a scale
Standard Deviation 1.27
|
PRIMARY outcome
Timeframe: 9-monthsService member self-reported stress; Likert-type scale 0 = Never to 4 = Very often, combined to a mean score, with a possible range from 0 to 4. Higher scores indicate greater stress (worse). Source: Cohen \& Williamson, 1988
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=253 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=260 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Perceived Stress Scale
|
1.35 score on a scale
Standard Deviation .71
|
1.38 score on a scale
Standard Deviation .67
|
PRIMARY outcome
Timeframe: 9-monthsService member difficulty with completing work tasks and quality; 6 items with Likert-type responses: 1 = No difficulty at all to 5 = Extreme difficulty, mean score created from all items, with possible score range from 1 to 5. Higher levels indicating greater impairment (worse). Source: Subscale of Overall Functional Impairment by Herrell et al., 2014
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=252 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=259 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Walter Reed Functional Impairment: Occupational Subscale (OFI)
|
1.79 score on a scale
Standard Deviation .77
|
1.73 score on a scale
Standard Deviation .76
|
PRIMARY outcome
Timeframe: 9-monthsService member difficulty with getting personal life skills completed; 2 items with Likert-type responses: 1 = No difficulty at all to 5 = Extreme difficulty, mean score created from all items, with possible score range from 1 to 5. Higher levels indicating greater impairment (worse). Source: Subscale of Overall Functional Impairment by Herrell et al., 2014
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=253 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=260 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Walter Reed Functional Impairment Scale: Personal Functioning Subscale (PFI)
|
1.66 score on a scale
Standard Deviation .67
|
1.68 score on a scale
Standard Deviation .69
|
PRIMARY outcome
Timeframe: 9-monthsService member difficulty functioning in social situations; 4 items with Likert-type responses: 1 = No difficulty at all to 5 = Extreme difficulty, mean score created from all items, with possible score range from 1 to 5. Higher levels indicating greater impairment (worse). Source: Subscale of Overall Functional Impairment by Herrell et al., 2014
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=252 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=256 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Walter Reed Functional Impairment Scale: Social Functional Impairment Subscale (SFI)
|
1.55 score on a scale
Standard Deviation .70
|
1.54 score on a scale
Standard Deviation .68
|
SECONDARY outcome
Timeframe: 4-monthsPerceived supervisor support for work-family integration as reported by service member, 4 items, with responses on Likert-type scale 1=Strongly disagree to 5= Strongly agree, overall score created by mean score, with possible scores ranging from 1 to 5.. Higher scores indicating higher levels of support (better) Source: Hammer et al., 2013
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=286 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=283 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Family Supportive Supervisor Behaviors (FSSB)
|
4.12 score on a scale
Standard Deviation .91
|
3.98 score on a scale
Standard Deviation .94
|
SECONDARY outcome
Timeframe: 4-monthsPerceived supervisor support for sleep health as reported by service member, 8 items, with responses on Likert-type scale 1=Never to 5= Always, overall score created by mean score, with possible scores ranging from 1 to 5.. Higher scores indicating higher levels of support (better) Source: Modified version of Gunia et al., 2015
Outcome measures
| Measure |
Intervention Combined: Service Member/Employees
n=283 Participants
Includes all service members/employees who are in the intervention condition, which includes both treatments: 1) Their supervisor is in the condition for the Sleep Leadership/FSSB training and 2) the service member is in the sleep actigraphy feedback condition.
|
Waitlist Control
n=284 Participants
Service members do not receive actigraphy feedback NOR do their supervisors receive the sleep leadership/FSSB training until AFTER final data collection at 9 months
|
|---|---|---|
|
Sleep Leadership
|
2.54 score on a scale
Standard Deviation 1.05
|
2.32 score on a scale
Standard Deviation .95
|
Adverse Events
Intervention Combined: Service Member/Employees
Waitlist Control
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Dr. Leslie Hammer, PI
Oregon Health & Science University
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place