Readiness Supportive Leadership Training (RESULT)

March 8, 2022 updated by: Leslie Hammer, Oregon Health and Science University

Behavioral Health & Resilience Training for Military Leaders

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.

Study Overview

Status

Active, not recruiting

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 Type

Interventional

Enrollment (Actual)

2297

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Washington
      • Tacoma, Washington, United States, 98433
        • Joint Base Lewis McChord

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

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:

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: DOUBLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Leader Intervention
Leaders in the intervention group will go through the 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Leader reactions to RESULT training
Time Frame: 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.
10 minutes post-training
Training Knowledge
Time Frame: 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.
10 minutes post-training
Leader general self-efficacy
Time Frame: 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.
10 minutes post-training
Mental health self-efficacy
Time Frame: 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.
10 minutes post-training
Mental illness stigma
Time Frame: 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.
10 minutes post-training
Resilience supportive supervisor behaviors
Time Frame: 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.
6-month post intervention
Organizational attachment
Time Frame: 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.
6-month post intervention
Emotion Regulation
Time Frame: 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.
6-month post intervention
Resilience
Time Frame: 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.
6-month post intervention
Social connectedness
Time Frame: 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.
6-month post intervention
Psychological health
Time Frame: 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.
6-month post intervention
Physical health
Time Frame: 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.
6-month post intervention
Cohesion
Time Frame: 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.
6-month post intervention
Combat exposure
Time Frame: 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.
6-month post intervention
Demographics
Time Frame: 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.
6-month post intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

September 3, 2020

Primary Completion (ACTUAL)

February 8, 2021

Study Completion (ANTICIPATED)

August 1, 2022

Study Registration Dates

First Submitted

October 18, 2019

First Submitted That Met QC Criteria

November 4, 2019

First Posted (ACTUAL)

November 5, 2019

Study Record Updates

Last Update Posted (ACTUAL)

March 10, 2022

Last Update Submitted That Met QC Criteria

March 8, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • W81XWH-18-PHTBIRP-R2OE-TRA

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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