NCT06205186

Brief Summary

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.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
400

participants targeted

Target at P75+ for not_applicable

Timeline
8mo left

Started Mar 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress77%
Mar 2024Jan 2027

First Submitted

Initial submission to the registry

December 19, 2023

Completed
24 days until next milestone

First Posted

Study publicly available on registry

January 12, 2024

Completed
2 months until next milestone

Study Start

First participant enrolled

March 8, 2024

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 15, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 15, 2027

Last Updated

April 27, 2025

Status Verified

April 1, 2025

Enrollment Period

2.9 years

First QC Date

December 19, 2023

Last Update Submit

April 23, 2025

Conditions

Health Behavior

Keywords

SoldierResilience

Outcome Measures

Primary Outcomes (16)

  • Resilience

    Connor Davidson Resilience Scale (CDRISC)

    1 month

  • Resilience

    Brief Resilience Scale (BRS)

    1 month

  • Emotion Regulation

    Difficulty in Emotion Regulation Scale (DERS)

    1 month

  • Experiential Avoidance

    Multidimensional Experiential Avoidance Questionnaire (MEAQ-30)

    1 month

  • Intolerance of Uncertainty

    Intolerance of Uncertainty Scale (IUS-12)

    1 month

  • Coping

    Brief COPE

    1 month

  • Positive and Negative Social Exchanges

    Positive and Negative Social Exchanges (PANSE)

    1 month

  • Post Traumatic Stress Disorder (PTSD)

    PTSD Checklist (PCL-5)

    1 month

  • Sleep

    Pittsburgh Sleep Quality Index (PSQI)

    1 month

  • Social Support

    Social Support Survey (SSS)

    1 month

  • Responses to Stressful Experiences

    Responses to Stressful Experiences Scale (RSES)

    1 month

  • Unit Cohesion

    Questionnaire

    1 month

  • Depression

    Patient Health Questionnaire (PHQ-8)

    2 weeks

  • Anxiety

    Generalized Anxiety Disorder (GAD7)

    2 weeks

  • Stress

    Perceived Stress Scale (PSS)

    1 month

  • Drug Abuse

    Drug Abuse Screening Test (DAST-10)

    12 months

Secondary Outcomes (3)

  • Topics Ranking

    1 month

  • Technology Use

    1 month

  • Program Satisfaction

    6 Months

Study Arms (1)

Program Users

OTHER
Behavioral: Army Health

Interventions

Army HealthBEHAVIORAL

A whole health mobile application for Soldiers

Program Users

Eligibility Criteria

Age21 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Pennington Biomedical Research Center

Baton Rouge, Louisiana, 70808, United States

RECRUITING

MeSH Terms

Conditions

Health Behavior

Condition Hierarchy (Ancestors)

Behavior

Central Study Contacts

Nicole Wesley

CONTACT

2257632721nicole.wesley@pbrc.edu

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

December 19, 2023

First Posted

January 12, 2024

Study Start

March 8, 2024

Primary Completion (Estimated)

January 15, 2027

Study Completion (Estimated)

January 15, 2027

Last Updated

April 27, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

Locations

US(1)