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Oregon Military Employee Sleep and Health Study

Not Applicable
Completed
Conditions
Health Behavior
Well-Being
Sleep
Interventions
Behavioral: FSSB/Sleep Leadership Training
Behavioral: Actigraphy Feedback
Registration Number
NCT02946736
Lead Sponsor
Oregon Health and Science University
Brief Summary

This study is a randomized controlled trial that will assess the effects of (1) the Family-Supportive Supervisor Behavior (FSSB) and Sleep Leadership training and (2) sleep/cognitive effectiveness feedback intervention on health and well-being among full-time employees in the Oregon National Guard, their supervisors, and their families. The interventions involving both health protection and health promotion are expected to contribute to improvements in employees' and their supervisors' sleep, risk behaviors, mental and physical health, and injury, as well as employees' and their spouse/partners' family experiences, health and well-being, and workplace outcomes.

Detailed Description

The overall goal of the Military Employee Sleep and Health (MESH) study is to improve safety, health and well-being of service members in the Oregon National Guard and their families. The MESH Study seeks to do this by training supervisors to support Oregon National Guard service members by focusing on a reduction in work-life stress while increasing sleep health.

The Oregon MESH Study proposes that leadership can influence a fundamental change in the recognition of sleep health and service members' overall well-being and the well-being of their family members. With the support of the Oregon National Guard, the MESH Study will provide family-support and sleep leadership training for supervisors while raising awareness of sleep through daily non-invasive sleep measurements.

The investigators of the Oregon MESH Study expect positive results for study participants, including reduced stress and increased social support. Longer term, these effects are expected to create a more supportive work environment, which has positive effects on safety, health, well-being, family, and organizational outcomes. The investigators also expect that providing service members with individual sleep feedback will reduce sleep problems and improve sleep awareness.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1284
Inclusion Criteria
  • Full-time employees in the Oregon National Guard, including Military Technicians and Active Guard Reserves.
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Exclusion Criteria
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Supervisor InterventionFSSB/Sleep Leadership TrainingSupervisors in the intervention group will go through the FSSB/sleep leadership training and receive actigraphy feedback.
Supervisor InterventionActigraphy FeedbackSupervisors in the intervention group will go through the FSSB/sleep leadership training and receive actigraphy feedback.
Employee InterventionActigraphy FeedbackEmployees in the intervention group will receive actigraphy feedback.
Primary Outcome Measures
NameTimeMethod
Change in Sleep Quality as assessed by the PROMIS Scale of Sleep-Related ImpairmentChange from Baseline Sleep Quality at 9-month post-baseline

PROMIS: Patient-Reported Outcomes Measurement Information System;

All items will be averaged to compute scale scores.

Change in Perceived Health as assessed by Hobfoll et al.'s (2012) Perceived Health ScaleChange from Baseline Perceived Health at 9-month post-baseline
Change in Sleep Quality as assessed by the PROMIS Scale of Sleep DisturbanceChange from Baseline Sleep Quality at 9-month post-baseline

PROMIS: Patient-Reported Outcomes Measurement Information System;

All items will be averaged to compute scale scores.

Change in Sleep Patterns as assessed by objective actigraphic measurementsChange from Baseline Sleep Patterns at 9-month post-baseline

Actigraphic measurements are obtained using Actiwatch2

Change in Work-Family Conflict as assessed by Matthews et al.'s (2010) Work-Family Conflict ScaleChange from Baseline Work-Family Conflict at 9-month post-baseline
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Oregon Health & Science University

🇺🇸

Portland, Oregon, United States

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