Evaluation of the Readiness Supportive Leadership Training - National Guard
RESULT-NG
Evaluating the Effectiveness of Leadership Training for Preventing Risk Factors and Promoting Protective Factors Contributing to Psychological Health
1 other identifier
interventional
5,400
0 countries
N/A
Brief Summary
The goal of this randomized clinical trial is to evaluate an intervention aimed at increasing the support leaders in the National Guard provide to their subordinates to promote mental health and well-being and reduce risk factors. Survey data will be collected from leaders, service members (SMs) and spouse/partners to evaluate the training effectiveness. The primary objective of the trial is to demonstrate efficacy in the NG, including effects on leaders, SMs, and spouse/partners on the following outcomes: H1: Leaders in the intervention group will demonstrate significant improvements in digital learning effects from pre-test to post-test. H2: The intervention will significantly decrease SM and Leader reports of problematic anger, loneliness, and psychological distress 6-months and then 12-months post-baseline. H3: Spouses/partners of SMs in the intervention group will report decreases in problematic anger, loneliness, and psychological distress at 6 and 12 months. Researchers will compare those in the training intervention group to a wait-list control group. The leadership training builds on a training evaluated in a previous RCT (NCT04152824) adapting from active duty Army to National Guard, including Air NG, and adding an additional facilitated session component. The intervention will include: (1) a 1-hour digital learning utilizing an interactive and self-paced computer-based training, (2) an behavior tracking exercise, and (3) a 1-hour facilitated session, approximately one month later.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Feb 2026
Longer than P75 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 24, 2025
CompletedFirst Posted
Study publicly available on registry
October 2, 2025
CompletedStudy Start
First participant enrolled
February 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 30, 2029
October 2, 2025
September 1, 2025
1.7 years
September 24, 2025
September 24, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Dimensions of Anger (DAR-5)
Each item in the scale uses a 5-point Likert scale (1 = none of the time, 2 = a little of the time, 3 = some of the time, 4 = most of the time, and 5 = all of the time). A cutoff score of 8 or greater on the DAR-3 is considered indicative of problematic anger and shows optimal sensitivity and specificity.
0 months, 6 months, and 12 months
Depression Subscale- Primary Health Questionnaire (PHQ-9)
Nine item questionnaire based on the diagnostic criteria for major depressive disorder in the DSM-5. Each question is scored on a scale of 0 to 3, with higher scores indicating greater symptom severity.
0 months, 6 months, and 12 months
Brief Loneliness Scale
3-item scale. Responses are summed to calculate a total score between 3 and 9. Lower scores (3-5) indicate less loneliness, while higher scores (6-9) suggest more significant feelings of loneliness.
0 months, 6 months, and 12 months.
Study Arms (2)
Leadership Training Intervention
EXPERIMENTALIncludes leaders, service members, and their spouse/partners where applicable whose units were randomized to receive the RESULT-NG training
Wait-list Control
NO INTERVENTIONThe Waitlist Control Arm serves as a delayed start arm. During months 0-15, the waitlist control arm acts as usual practice/no intervention comparator. During months 16-21 (i.e. after final data collection), the waitlist control warm will receive the intervention.
Interventions
RESULT-NG is a multi-level intervention where leaders receive the training intervention, with evaluation of effects at the subordinate, leader and spouse levels. RESULT-NG consists of three distinct but related components: 1) a 60-minute, multimedia, interactive digital-learning training session, 2) a two-week behavior tracking exercise that takes less than 2 minutes/day after the digital learning to put what was learned into practice, and 3) a 60-minute facilitated session, either in person or virtual, with trained staff embedded within the National Guard.
Eligibility Criteria
You may qualify if:
- years of age (adults)
- Employed as a member of the Oregon National Guard (ORNG), including Title 5 and 32 civilians, or is a spouse/partner of an ORNG service member married or cohabitating with the SM for 6 months or more
You may not qualify if:
- Under 18 years of age
- Not employed as a member of the Oregon National Guard (ORNG), including Title 5 and 32 civilians, or is a spouse/partner of an ORNG service member married or cohabitating with the SM for less than 6 months
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Director of Applied Research
Study Record Dates
First Submitted
September 24, 2025
First Posted
October 2, 2025
Study Start
February 1, 2026
Primary Completion (Estimated)
November 1, 2027
Study Completion (Estimated)
June 30, 2029
Last Updated
October 2, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
All deidentified IPD collected throughout the trial.