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

NCT ID: NCT06608979

Last Updated: 2024-09-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-06-11

Study Completion Date

2025-03-31

Brief Summary

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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.

Detailed Description

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The majority of women entering substance use treatment have a trauma history, placing them at risk for revictimization and substance use relapse. 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, trauma-focused 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 demographics, trauma and sexual assault experiences, knowledge and attitudes towards sexual and intimate partner violence, protective behavioral strategies, and intervention satisfaction and engagement.

Conditions

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

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Single arm design with baseline, posttest, and follow-up assessments
Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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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.

Group Type EXPERIMENTAL

Screening/Referral and Prevention

Intervention Type 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)

Interventions

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Screening/Referral and Prevention

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)

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1\) Age 18 or higher;2) female gender identity; 3) currently engaged in substance use treatment or care (behavioral, peer support, pharmacological, medical)

\-

Exclusion Criteria

1\) Non-English-speaking; 2) acute physical and medical conditions that interfere with participation in educational sessions (e.g., active psychosis, suicidality).

\-
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Prisma Health-Upstate

OTHER

Sponsor Role collaborator

Clemson University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Heidi Zinzow, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Clemson University

Locations

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Addiction Medicine Clinic, Prisma Health Upstate

Greenville, South Carolina, United States

Site Status RECRUITING

The Phoenix Center

Greenville, South Carolina, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Heidi Zinzow, Ph.D.

Role: CONTACT

864-656-4376

Lauren Smalls, B.S.

Role: CONTACT

864-656-3210

Facility Contacts

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Leigh Huckins

Role: primary

864-643-8567

Kimbley Smith

Role: primary

864-467-3790

References

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Zinzow HM, Pericot-Valverde I, Smalls L, Brancato MG, Chapman G, Smith A, Thompson A, Greco C, Shank M, Eichelberger KY, Smith K, Litwin AH. A Peer Support Specialist-Delivered Sexual and Intimate Partner Violence Prevention Program for Women in Substance Use Treatment: Protocol for a Single-Arm Trial. JMIR Res Protoc. 2025 Aug 8;14:e68673. doi: 10.2196/68673.

Reference Type DERIVED
PMID: 40779309 (View on PubMed)

Other Identifiers

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2016636

Identifier Type: -

Identifier Source: org_study_id

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