MESH: Oregon Military Employee Sleep and Health Study

Sponsor
Oregon Health and Science University (Other)
Overall Status
Completed
CT.gov ID
NCT02946736
Collaborator
Portland State University (Other), Colorado State University (Other), United States Department of Defense (U.S. Fed)
1,284
1
2
40.5
31.7

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: FSSB/Sleep Leadership Training
  • Behavioral: Actigraphy Feedback
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
1284 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Prevention
Official Title:
Evaluation of a Work-Family and Sleep Leadership Intervention in the Oregon National Guard: A Behavioral Health Leadership Approach
Actual Study Start Date :
Jul 21, 2017
Actual Primary Completion Date :
May 22, 2020
Actual Study Completion Date :
Dec 4, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Supervisor Intervention

Supervisors in the intervention group will go through the FSSB/sleep leadership training and receive actigraphy feedback.

Behavioral: FSSB/Sleep Leadership Training
Supervisors will receive a training addressing family-supportive supervisor behaviors and sleep leadership.

Behavioral: Actigraphy Feedback
Supervisors and employees will receive personalized feedback on their sleep and activity measurements.

Experimental: Employee Intervention

Employees in the intervention group will receive actigraphy feedback.

Behavioral: Actigraphy Feedback
Supervisors and employees will receive personalized feedback on their sleep and activity measurements.

Outcome Measures

Primary Outcome Measures

  1. Change in Sleep Quality as assessed by the PROMIS Scale of Sleep-Related Impairment [Change from Baseline Sleep Quality at 4-month post-baseline]

    PROMIS: Patient-Reported Outcomes Measurement Information System; All items will be averaged to compute scale scores.

  2. Change in Sleep Quality as assessed by the PROMIS Scale of Sleep-Related Impairment [Change 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.

  3. Change in Sleep Patterns as assessed by objective actigraphic measurements [Change from Baseline Sleep Patterns at 4-month post-baseline]

    Actigraphic measurements are obtained using Actiwatch2

  4. Change in Sleep Patterns as assessed by objective actigraphic measurements [Change from Baseline Sleep Patterns at 9-month post-baseline]

    Actigraphic measurements are obtained using Actiwatch2

  5. Change in Perceived Health as assessed by Hobfoll et al.'s (2012) Perceived Health Scale [Change from Baseline Perceived Health at 4-month post-baseline]

  6. Change in Perceived Health as assessed by Hobfoll et al.'s (2012) Perceived Health Scale [Change from Baseline Perceived Health at 9-month post-baseline]

  7. Change in Work-Family Conflict as assessed by Matthews et al.'s (2010) Work-Family Conflict Scale [Change from Baseline Work-Family Conflict at 4-month post-baseline]

  8. Change in Work-Family Conflict as assessed by Matthews et al.'s (2010) Work-Family Conflict Scale [Change from Baseline Work-Family Conflict at 9-month post-baseline]

  9. Change in Sleep Quality as assessed by the PROMIS Scale of Sleep Disturbance [Change from Baseline Sleep Quality at 4-month post-baseline]

    PROMIS: Patient-Reported Outcomes Measurement Information System; All items will be averaged to compute scale scores.

  10. Change in Sleep Quality as assessed by the PROMIS Scale of Sleep Disturbance [Change 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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Full-time employees in the Oregon National Guard, including Military Technicians and Active Guard Reserves.
Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Oregon Health & Science University Portland Oregon United States 97239

Sponsors and Collaborators

  • Oregon Health and Science University
  • Portland State University
  • Colorado State University
  • United States Department of Defense

Investigators

  • Principal Investigator: Leslie Hammer, PhD, Oregon Health and Science University

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Leslie Hammer, Professor, Oregon Health and Science University
ClinicalTrials.gov Identifier:
NCT02946736
Other Study ID Numbers:
  • W81XWH-16-1-0720
First Posted:
Oct 27, 2016
Last Update Posted:
Feb 24, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Leslie Hammer, Professor, Oregon Health and Science University

Study Results

No Results Posted as of Feb 24, 2021