Transition Health and Resilience Through Valued Experiences (THRiVE) Pilot for Newly Separated Veterans

Part of paid clinical trials in Durham, North Carolina.

Sponsor
RTI International
Study ID
NCT06778278
Status
Recruiting
Apply to this trial

Conditions

  • Alcohol Misuse
  • Community Reintegration
  • Mental Health
  • Military Transition
  • Suicidal Ideation

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Transition Health and Resilience through Valued Experiences (THRiVE) Program — BEHAVIORAL
    Six (6) total weekly, 90-minute, small-group, peer-led sessions delivered virtually

Study Details

The objective of this study is to develop and pilot a program designed to improve mental health outcomes and reduce suicide risk during the transition from military to civilian life. It is hypothesized that the Transition Health and Resilience through Valued Experiences (THRiVE) program, to be developed as part of this study, will meet participant recruitment, retention, and satisfaction benchmarks (primary outcomes) and show positive preliminary effects on mental health symptoms, risk factors for suicidal ideation, and psychosocial functioning outcomes (secondary outcomes). The specific aims of this study are to: 1. Develop a small-group, peer-led, cross-cutting prevention program for newly separated veterans (NSVs) called THRiVE and 2. Evaluate the feasibility, acceptability, and preliminary effects of the THRiVE program on mental health symptoms, risk factors for suicidal ideation, and psychosocial functioning outcomes. Up to 40 NSVs participating in this Stage 1 pilot study will complete validated self-report measures at baseline, immediately after completing the THRiVE program (post-THRiVE), and 3 months after completing the THRiVE program (follow-up). The duration of a participant's time in the study is anticipated to be 5 months.

Key Dates

Start date
Jul 30, 2025
Status verified
Jan 2026
Primary completion
Oct 31, 2026
Completion
Oct 31, 2026

Study Design

Enrollment
40 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION

Arms

  • Experimental: THRiVE

Primary Outcome Measure

Participant recruitment rate [ Time Frame: 14 months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
RTI InternationalDurhamNorth Carolina27713
Principal Investigator
[email protected]
919-485-5427
Shannon M Blakey, PhD (PRINCIPAL_INVESTIGATOR)

Find similar trials in Durham, NC

By research site
RTI International· Durham, NC

Related Studies