Actively Recruiting
Trauma Screening/Referral and Interpersonal Violence Prevention for Women with Substance Use Disorders
Led by Clemson University · Updated on 2024-09-23
60
Participants Needed
2
Research Sites
N/A
Total Duration
On this page
Sponsors
C
Clemson University
Lead Sponsor
P
Prisma Health-Upstate
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to evaluate a peer support specialist-delivered violence prevention program for women in substance use treatment who often have trauma histories that increase their risk of revictimization and relapse. The study focuses on the feasibility and preliminary effects of a program that includes posttraumatic stress disorder (PTSD) screening, trauma-focused resource referrals, and a two-session interpersonal violence prevention protocol for 60 women. Participants receive a brief PTSD screening and, if positive, are connected to trauma-focused resources. They then attend two one-hour sessions led by peer support specialists: the first covers PTSD screening and education on interpersonal violence including consent and intimate partner violence, and the second focuses on protective behavioral strategies for violence prevention. Women complete assessments at baseline, immediately after the intervention, one month, and three months later. These include self-report surveys on trauma exposure, attitudes toward violence, coping strategies, and resource use. Researchers measure outcomes such as acceptance of rape myths, dating violence attitudes, sexual aggression coping, and substance use. The total participation spans about three months with ongoing monitoring of intervention engagement and satisfaction.
CONDITIONS
Brief Title
Trauma Screening/Referral and Interpersonal Violence Prevention for Women with Substance Use Disorders
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 or higher
- Female gender identity
- Currently engaged in substance use treatment or care (behavioral, peer support, pharmacological, medical)
You will not qualify if you...
- Non-English-speaking
- Acute physical and medical conditions that interfere with participation in educational sessions (e.g., active psychosis, suicidality)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person)
Duration - 2 weeks
Participants receive a brief PTSD screening/referral and participate in two one-hour peer support specialist-delivered educational sessions on interpersonal violence prevention.
2 sessions over 2 weeks (in-person)
Duration - 16 weeks
Participants complete follow-up assessments to monitor knowledge, attitudes, and experiences related to interpersonal violence prevention.
3 visits at post-intervention (2 weeks), 1 month (6 weeks), and 3 months (18 weeks) follow-ups
Trial Site Locations
Total: 2 locations
1
Addiction Medicine Clinic, Prisma Health Upstate
Greenville, South Carolina, United States, 29605
Actively Recruiting
2
The Phoenix Center
Greenville, South Carolina, United States, 29607
Actively Recruiting
Research Team
H
Heidi Zinzow, Ph.D.
L
Lauren Smalls, B.S.
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1