ClinicalTrials.Veeva

Menu

Evaluation of the Readiness Supportive Leadership Training - National Guard (RESULT-NG)

Oregon Health & Science University (OHSU) logo

Oregon Health & Science University (OHSU)

Status

Not yet enrolling

Conditions

Anger Problems
Loneliness
Psychological Distress

Treatments

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

Study type

Interventional

Funder types

Other

Identifiers

NCT07203170
HT9425-25-1-0668

Details and patient eligibility

About

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.

Enrollment

5,400 estimated patients

Sex

All

Ages

18 to 89 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18 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

Exclusion criteria

  • 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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

5,400 participants in 2 patient groups

Leadership Training Intervention
Experimental group
Description:
Includes leaders, service members, and their spouse/partners where applicable whose units were randomized to receive the RESULT-NG training
Treatment:
Behavioral: Readiness Supportive Leadership Training for the National Guard (RESULT-NG)
Wait-list Control
No Intervention group
Description:
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.

Trial contacts and locations

0

Loading...

Central trial contact

Krista Brockwood, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems