- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04152824
Readiness Supportive Leadership Training (RESULT)
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
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Washington
-
Tacoma, Washington, United States, 98433
- Joint Base Lewis McChord
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Collaborators
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- W81XWH-18-PHTBIRP-R2OE-TRA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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