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Not yet recruiting NCT07203170

Evaluation of the Readiness Supportive Leadership Training - National Guard

No phase Interventional Psychological Distress Anger Problems Loneliness

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Readiness Supportive Leadership Training for the National Guard (RESULT-NG).
Who it may be relevant to
Registry conditions: Psychological Distress, Anger Problems, Loneliness. Basic parameters: 18 years — 89 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Evaluating the Effectiveness of Leadership Training for Preventing Risk Factors and Promoting Protective Factors Contributing to Psychological Health

Overview

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.

Interventions

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

Primary outcome measures

  • Dimensions of Anger (DAR-5) [Time frame: 0 months, 6 months, and 12 months]
  • Depression Subscale- Primary Health Questionnaire (PHQ-9) [Time frame: 0 months, 6 months, and 12 months]
  • Brief Loneliness Scale [Time frame: 0 months, 6 months, and 12 months.]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Prevention

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07203170 · HT9425-25-1-0668

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗