Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
ID06608979

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

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

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)
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit (in-person)

Outpatient Treatment

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)

Follow-up

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

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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

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Published Research Related To This Trial

A Peer Support Specialist-Delivered Sexual and Intimate Partner Violence Prevention Program for Women in Substance Use Treatment: Protocol for a Single-Arm Trial.

Heidi M Zinzow, Irene Pericot-Valverde, Lauren Smalls...

https://pubmed.ncbi.nlm.nih.gov/40779309