RESULT: Readiness Supportive Leadership Training

Sponsor
Oregon Health and Science University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04152824
Collaborator
Portland State University (Other)
2,297
1
2
22.9
100.3

Study Details

Study Description

Brief Summary

This study is a randomized controlled trial that will assess the effects of an evidence based, multi-component, leadership support intervention, Resilience-Supportive Leadership Training (RESULT), using accelerated learning strategies aimed at improving Service Member resilience and readiness in the military.

The intervention is expected to increase perceptions of resilience-supportive behaviors, resilience indicators, and related behavioral health outcomes such as emotion regulation, connectedness, team cohesion, psychological health, and physical health following the training from the perspective of the Service Member.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Resilience-Supportive Leadership Training (RESULT)
N/A

Detailed Description

The goal of our proposed study is to adapt our existing, evidence-based supportive leadership training for an active duty population, focusing on training junior leaders in the Army on ways they can enhance readiness and resilience in their soldiers, as well as their own resilience. The investigators will draw on best practices from existing military and civilian programs in a training that is engaging, interactive, and customizable. The investigators will use micro-learnings - small, bite-sized pieces of information delivered in non-traditional ways, such as short podcasts or videos to enhance the training and enable it to be integrated easily into both military and civilian jobs.

The investigators will evaluate the effectiveness of our Resilience-Supportive Leadership Training (RESULT) intervention with U.S. Army soldiers stationed at Joint Base Lewis-McChord (JBLM) in the State of Washington. The study will include a control group, so The investigators can better determine whether any observed changes in our participants are due to our training programs, and not some other factor. The investigators anticipate that the training programs will have a positive impact on service member readiness and resilience, psychological health, team cohesion, and reduced loneliness.

This research is designed to benefit not only U.S. Army soldiers but across all military branches, as well as first-responders and other civilian occupations that face highly stressful situations as part of their work. Our training will have the potential to positively contribute to the military by enhancing service member readiness and unit autonomy, and improving mental and physical health.

Study Design

Study Type:
Interventional
Actual Enrollment :
2297 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Prevention
Official Title:
Behavioral Health & Resilience Training for Military Leaders
Actual Study Start Date :
Sep 3, 2020
Actual Primary Completion Date :
Feb 8, 2021
Anticipated Study Completion Date :
Aug 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Leader Intervention

Leaders in the intervention group will go through the Resilience-Supportive Leadership Training (RESULT)

Behavioral: Resilience-Supportive Leadership Training (RESULT)
Leaders will receive a training addressing supportive supervisor behaviors and resilience

No Intervention: Control Group

Leaders in the control group will be usual practice

Outcome Measures

Primary Outcome Measures

  1. Leader reactions to RESULT training [10 minutes post-training]

    Leader perceptions of training effectiveness, usefulness, and recommendations of training. Survey responses on likert-type scales. Anonymized individual data will be collected. Data will be reported at the mean.

  2. Training Knowledge [10 minutes post-training]

    Leader knowledge of resilience leadership and mental health knowledge; demonstrating knowledge acquisition from training content. Survey responses on likert-type scales (e.g., not at all - very much; strongly disagree - strongly agree). Anonymized individual data will be collected. Data will be reported at the mean.

  3. Leader general self-efficacy [10 minutes post-training]

    Leader belief that they can effectively execute behaviors to obtain important outcomes. Survey responses on likert-type scales. Anonymized individual data will be collected. Data will be reported at the mean.

  4. Mental health self-efficacy [10 minutes post-training]

    Leader belief that they can effectively execute behaviors to obtain mental health outcomes. Survey responses on likert-type scales. Anonymized individual data will be collected. Data will be reported at the mean.

  5. Mental illness stigma [10 minutes post-training]

    Leader perceptions of mental illness stigma. Survey responses on likert-type scales. Anonymized individual data will be collected. Data will be reported at the mean.

  6. Resilience supportive supervisor behaviors [6-month post intervention]

    Service member's perceptions of leadership behaviors supporting resilience and mental health, general effectiveness, and general supervisor support. Survey responses on likert-type scales. Anonymized individual data will be collected. Data will be reported at the mean.

  7. Organizational attachment [6-month post intervention]

    Organizational attachment Description: Service member's perceptions of organizational commitment. Survey responses on likert-type scales. Anonymized individual data will be collected. Data will be reported at the mean.

  8. Emotion Regulation [6-month post intervention]

    Service member's perceptions of regulation or suppression of emotions. Survey responses on likert-type scales. Anonymized individual data will be collected. Data will be reported at the mean.

  9. Resilience [6-month post intervention]

    Service member's perceptions of the effectiveness in which they cope with problems in life. Survey responses on likert-type scales. Anonymized individual data will be collected. Data will be reported at the mean.

  10. Social connectedness [6-month post intervention]

    Service member's perceptions of belongingness and loneliness. Survey responses on likert-type scales. Anonymized individual data will be collected. Data will be reported at the mean.

  11. Psychological health [6-month post intervention]

    Service member's perceptions of their psychological health including distress, impairment in functional life areas, stress, PTSD symptoms, and anger. Survey responses on likert-type scales. Anonymized individual data will be collected. Data will be reported at the mean.

  12. Physical health [6-month post intervention]

    Service member's perceptions of physical health. Survey responses on likert-type or continuous scales. Anonymized individual data will be collected. Data will be reported at the mean.

  13. Cohesion [6-month post intervention]

    Service member's reported exposure to combat experiences during their military tenure. Survey responses on a count scale (never - 5 or more times). Anonymized individual data will be collected. Data will be reported at the mean.

  14. Combat exposure [6-month post intervention]

    Service member's reported exposure to combat experiences during their military tenure. Survey responses on a count scale (never - 5 or more times). Anonymized individual data will be collected. Data will be reported at the mean.

  15. Demographics [6-month post intervention]

    Leader and service member demographics including unit information, age, rank, gender, relationship status, number of children, years in the military, deployment history, and months in platoon. Survey responses. Anonymized individual data will be collected. Data will reported with mean or percentages.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Active Duty Service Members Serving in one of the two Striker Brigade Combat Teams (SBCT), Positions of platoon leader or below.

Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Joint Base Lewis McChord Tacoma Washington United States 98433

Sponsors and Collaborators

  • Oregon Health and Science University
  • Portland State University

Investigators

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

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Leslie Hammer, Principal Investigator, Oregon Health and Science University
ClinicalTrials.gov Identifier:
NCT04152824
Other Study ID Numbers:
  • W81XWH-18-PHTBIRP-R2OE-TRA
First Posted:
Nov 5, 2019
Last Update Posted:
Mar 10, 2022
Last Verified:
Mar 1, 2022
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, Principal Investigator, Oregon Health and Science University

Study Results

No Results Posted as of Mar 10, 2022