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.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

704 participants

Primary outcome timeframe

4 months

Results posted on

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

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

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 months

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.

Outcome measures

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 months

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.

Outcome measures

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 months

Four 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

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 months

Four 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

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 months

Four 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

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 months

Four 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

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 months

8 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

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 months

8 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

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 months

Actigraphic 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

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-months

Actigraphic 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

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-months

Service 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

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-months

Service 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

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-months

Service 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

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-months

Service 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

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-months

Service 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

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-months

Service 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

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-months

Perceived 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

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-months

Perceived 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

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

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

Waitlist Control

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. Leslie Hammer, PI

Oregon Health & Science University

Phone: 503-494-9313

Results disclosure agreements

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