RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2024-06-11
Study Completion:2025-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06608979

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Heidi Zinzow, Ph.D.
CONTACT
864-656-4376
hzinzow@clemson.edu
Lauren Smalls, B.S.
CONTACT
864-656-3210
ltsmall@clemson.edu

Principal Investigator

Heidi Zinzow, Ph.D.
PRINCIPAL_INVESTIGATOR
Clemson University

Study Locations (Sites)

Addiction Medicine Clinic, Prisma Health Upstate
Greenville, South Carolina, 29605
United States
The Phoenix Center
Greenville, South Carolina, 29607
United States

Collaborators and Investigators

Sponsor: Clemson University

  • Heidi Zinzow, Ph.D., PRINCIPAL_INVESTIGATOR, Clemson University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-06-11
Study Completion Date2025-03

Study Record Updates

Study Start Date2024-06-11
Study Completion Date2025-03

Terms related to this study

Keywords Provided by Researchers

  • prevention
  • peer support specialist
  • substance use disorders
  • posttraumatic stress disorder
  • interpersonal violence
  • intimate partner violence
  • sexual violence

Additional Relevant MeSH Terms

  • Substance Use Disorders
  • Posttraumatic Stress Disorder
  • Opioid Use Disorder
  • Violence, Sexual
  • Violence, Gender-Based
  • Violence, Domestic