Trauma Screening/Referral and Interpersonal Violence Prevention for Women with Substance Use Disorders

Part of paid clinical trials in Greenville, South Carolina.

Sponsor
Clemson University
Study ID
NCT06608979
Status
Recruiting
Apply to this trial

Conditions

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Screening/Referral and Prevention — BEHAVIORAL
    Session 1: One hour PTSD Screening/referral and Psychoeducation on interpersonal violence (consent, drug-and-alcohol-facilitated assault, intimate partner violence); Session 2: One hour sessions on Protective Behavioral Strategies for interpersonal violence (skills training)

Study Details

The purpose of this project is to implement a pilot study to investigate the feasibility and preliminary efficacy of a peer support specialist delivered violence prevention program for women in substance use treatment. The program entails a posttraumatic stress disorder (PTSD) screening, resource referral, and two session interpersonal violence prevention protocol for 60 participants. In this single arm trial, women are recruited from three substance use treatment facilities. Participants complete baseline, post-intervention, one-month, and three-month follow-up assessments. Self-report surveys assess trauma exposure, knowledge and behaviors related to interpersonal violence, and intervention engagement.

Key Dates

Start date
Jun 11, 2024
Status verified
Jun 2024
Primary completion
Mar 31, 2025
Completion
Mar 31, 2025

Study Design

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

Arms

  • Experimental: Screening/Referral and Prevention
    Participants will receive a brief PTSD screening, warm handoff to trauma-focused resources if screening positive, and two session peer support specialist-delivered educational program on interpersonal violence prevention.

Primary Outcome Measure

ARC3 Consent Scale [ Time Frame: Participants complete this measure at baseline, post intervention (2 weeks), 1 month follow-up (6 weeks), and 3 month follow-up (18 weeks). ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Addiction Medicine Clinic, Prisma Health UpstateGreenvilleSouth Carolina29605
Leigh Huckins
[email protected]
864-643-8567
The Phoenix CenterGreenvilleSouth Carolina29607
Kimbley Smith
[email protected]
864-467-3790

Find similar trials in Greenville, SC

By condition
PTSD (post-traumatic stress disorder)
By specialty
PsychiatryMental healthBehavioral health
By research site
Addiction Medicine Clinic, Prisma Health Upstate· Greenville, SCThe Phoenix Center· Greenville, SC

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