NCT07203170

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

65
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
5,400

participants targeted

Target at P75+ for not_applicable

Timeline
39mo left

Started Feb 2026

Longer than P75 for not_applicable

Status
not yet recruiting

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

Study Progress8%
Feb 2026Jun 2029

First Submitted

Initial submission to the registry

September 24, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

October 2, 2025

Completed
4 months until next milestone

Study Start

First participant enrolled

February 1, 2026

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2027

Expected
1.7 years until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2029

Last Updated

October 2, 2025

Status Verified

September 1, 2025

Enrollment Period

1.7 years

First QC Date

September 24, 2025

Last Update Submit

September 24, 2025

Conditions

Keywords

MilitaryPsychological healthProblematic angerLeadershipResilienceTraining intervention

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

EXPERIMENTAL

Includes leaders, service members, and their spouse/partners where applicable whose units were randomized to receive the RESULT-NG training

Behavioral: Readiness Supportive Leadership Training for the National Guard (RESULT-NG)

Wait-list Control

NO INTERVENTION

The 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.

Leadership Training Intervention

Eligibility Criteria

Age18 Years - 89 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Psychological Well-Being

Condition Hierarchy (Ancestors)

Personal SatisfactionBehavior

Central Study Contacts

Krista Brockwood, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: This clinical trial uses a cluster-randomized Type I Hybrid design at the military unit level, with a wait-list control group.
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

All deidentified IPD collected throughout the trial.

Shared Documents
STUDY PROTOCOL
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