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Completed

NCT Number: NCT00998153

Risk Reduction for Drug Use and Sexual Revictimization

The investigator proposes to evaluate Risk Reduction through Family Therapy (RRFT), which integrates: 1) an ecologically-based intervention for treatment of substance abuse behaviors in high risk adolescents, 2) exposure-based cognitive-behavioral therapy for sexually assaulted youth, and 3) psychoeducation strategies for prevention of risky sexual behaviors and revictimization. The principal purpose of this research proposal is to evaluate the efficacy of RRFT in reducing the risk of drug abuse and other risky behaviors, PTSD, and revictimization among adolescents who have been sexually assaulted. The Research Plan will be conducted based on Stage 1a and Stage 1b from NIDA's Behavioral Therapies Development Program as described in Rounsaville, Carroll, & Onken (2001). The final phase of the research will involve conducting a pilot randomized controlled trial of RRFT in a sample of adolescents, comparing primary outcome measures of youth receiving RRFT to youth receiving usual care in the community. Participants will be adolescents (12-17 years) who have experienced a sexual assault. Assessment of substance use and other risk behaviors, trauma-related psychopathology, and incidents of revictimization will be collected at pre- and post- treatment, as well as 6-week and 3-month follow-ups. Hierarchical Linear Modeling will be the primary method used to test study hypotheses. Development and evaluation of the proposed intervention will have significant implications for addressing public health problems in adolescent substance abuse and related high risk behaviors.

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Key information

Age range

12 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

National Crime Victims Research and Treatment Center

Charleston, South Carolina, 29425, United States

About this study

See above summary

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • memorable sexual assault

Exclusion criteria

  • active psychosis
  • active suicidality

Treatment and study plan

Risk Reduction through Family Therapy

Behavioral

Component based intervention based on existing empirically supported treatments

Other names: RRFT

Primary outcomes

  1. Time Line Follow Back and urine screen

    Time frame: Pre and post-treatment, 3 and 6 month follow-ups

Secondary outcomes

  1. YRBS

    Time frame: Pre and post-treatment, 3 and 6 month follow-ups

  2. FES

    Time frame: Pre and post-treatment, 3 and 6 month follow-ups

  3. UCLA PTSD Reaction Index

    Time frame: Pre, post, and 3 and 6 month follow-up

Sponsors and collaborators

Lead sponsor

Medical University of South Carolina

Other

Collaborators

  • National Institute on Drug Abuse (NIDA)

Registry information

Acronym: RRFT

Important dates

Study start
2006
Primary completion
2011
Study completion
2012
First posted
Oct 20, 2009
Registry last updated
Jun 18, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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