NCT07050238

Brief Summary

The goal of the Life Force study is to (1) evaluate the efficacy of targeted, skills-based training for enhancing mental toughness and mitigating harmful and high-risk behaviors in active-duty Soldiers, and (2) to determine who benefits the most from this type of training. Researchers will compare the training group to a control group. All participants will complete a baseline survey and two follow up surveys at 6 and 12 months post-baseline. The group assigned to the Life Force training condition will also complete a 5-session, group-based, skills training program.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
2,400

participants targeted

Target at P75+ for not_applicable

Timeline
38mo left

Started Jan 2026

Longer than P75 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

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Study Timeline

Key milestones and dates

Study Progress10%
Jan 2026Jul 2029

First Submitted

Initial submission to the registry

June 25, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 3, 2025

Completed
6 months until next milestone

Study Start

First participant enrolled

January 6, 2026

Completed
2.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2028

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2029

Last Updated

April 28, 2026

Status Verified

May 1, 2025

Enrollment Period

2.5 years

First QC Date

June 25, 2025

Last Update Submit

April 27, 2026

Conditions

Keywords

Mental ToughnessActive-duty MilitaryRisk ReductionPrevention

Outcome Measures

Primary Outcomes (1)

  • Risky/Harmful Behaviors

    Self-reported or administratively recorded

    Within the 12 months following completion of the baseline assessment

Secondary Outcomes (5)

  • Poor Performance

    Within the 12 months following completion of the baseline assessment

  • Mental Toughness

    Within the 12 months following completion of the baseline assessment

  • Military Readiness, Satisfaction, & Career Plans

    Within the 12 months following completion of the baseline assessment

  • Suicide-related behaviors

    Within the 12 months following completion of the baseline assessment

  • Role Functioning (occupational, personal, and social)

    Within the 12 months following completion of the baseline assessment

Study Arms (2)

Life Force program

EXPERIMENTAL

The Life Force program is a 5-session, group-based, skills training program tailored specifically for active duty Soldiers. The program uses evidence-based strategies to mitigate harmful and high-risk behaviors and promote Mental Toughness.

Behavioral: Life Force

Control

NO INTERVENTION

Standard of care with 6- and 12-month follow up assessments.

Interventions

Life ForceBEHAVIORAL

5-session, group-based, skills training program tailored specifically for active-duty Soldiers aimed at mitigating harmful and high-risk behaviors and promote Mental Toughness.

Life Force program

Eligibility Criteria

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

You may qualify if:

  • Active duty Soldiers in the regular Army
  • Age 18 or older
  • Stationed at Fort Hood, TX

You may not qualify if:

  • Soldiers with self-identified plans of leaving active duty service within 12 months of the baseline assessment
  • Soldiers having a planned permanent change in station (PCS) or deployment within 12 months of the baseline assessment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Fort Hood

Killeen, Texas, 76544, United States

RECRUITING

MeSH Terms

Conditions

Risk Reduction Behavior

Condition Hierarchy (Ancestors)

Behavior

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
FED
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 25, 2025

First Posted

July 3, 2025

Study Start

January 6, 2026

Primary Completion (Estimated)

July 1, 2028

Study Completion (Estimated)

July 1, 2029

Last Updated

April 28, 2026

Record last verified: 2025-05

Locations