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Recruiting NCT06205186

Four Pillars of Defense: A Whole Health Approach to the Military

No phase Interventional Health Behavior

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: Army Health.
Who it may be relevant to
Registry conditions: Health Behavior. Basic parameters: from 21 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
United States
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 →

Overview

The overall objectives of this study are to better define the construct of psychological resilience in the military, to identify potential modifiable risk factors and trainable skills of psychological resilience in Soldiers, and provide a scalable, integrated physical and mental optimization training app to be integrated into relevant systems. The proposed work would be a first step in identifying predictive risk factors that can be modified to increase the future resilience of Soldiers. With this crucial information, the investigators aim to gather data that will inform the development of a resilience-focused intervention (e.g., a skills training program) and test the feasibility of that intervention.

Interventions

  • Behavioral Army Health
    A whole health mobile application for Soldiers

Primary outcome measures

  • Resilience [Time frame: 1 month]
  • Resilience [Time frame: 1 month]
  • Emotion Regulation [Time frame: 1 month]
  • Experiential Avoidance [Time frame: 1 month]
  • Intolerance of Uncertainty [Time frame: 1 month]
  • Coping [Time frame: 1 month]
  • Positive and Negative Social Exchanges [Time frame: 1 month]
  • Post Traumatic Stress Disorder (PTSD) [Time frame: 1 month]
  • Sleep [Time frame: 1 month]
  • Social Support [Time frame: 1 month]
Secondary outcome measures (3)
  • Topics Ranking [Time frame: 1 month]
  • Technology Use [Time frame: 1 month]
  • Program Satisfaction [Time frame: 6 Months]

Eligibility criteria

Inclusion criteria

  • Age 21+ and either a Soldier in the NG or NG family member

Exclusion criteria

  • Under age 21 and not an NG Soldier or family member

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

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Prevention

Study locations

United States · 1 center
  • Pennington Biomedical Research Center — Baton Rouge

Identifiers

NCT: NCT06205186 · PBRC 2023-073

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗