RRFT: Integrative Risk Reduction and Treatment for Teen Substance Use Problems and PTSD

Sponsor
Medical University of South Carolina (Other)
Overall Status
Completed
CT.gov ID
NCT01751035
Collaborator
National Institute on Drug Abuse (NIDA) (NIH)
135
1
2
68.3
2

Study Details

Study Description

Brief Summary

Adolescents receiving RRFT and their caregivers will report significantly fewer substance use problems (quantity of use, frequency of use, and abuse symptoms) during treatment and follow-up than control adolescents who receive Treatment as Usual (TAU). Adolescents receiving RRFT and their caregivers will report improvement in empirically-demonstrated risk and protective factors for substance use and abuse at the individual level (e.g., coping) and at each level of an adolescent's ecology (e.g., increased number of positive family activities, reduced family conflict, reduced number of peers who use drugs, improved school attendance, increased involvement in pro-social community activities) during treatment and follow-up than control adolescents who receive TAU. Adolescents receiving RRFT will experience less PTSD symptoms (per youth and caregiver reports) during treatment and follow-up than control adolescents who receive TAU. Adolescents receiving RRFT will report engaging in fewer risky sexual behaviors (e.g., increased condom use, fewer partners) during treatment and follow-up than control adolescents who receive TAU. Changes during treatment in family relations (familial cohesiveness and conflict, satisfaction with caregiver-youth relationship) and parenting practices (monitoring) will mediate changes in substance use. Changes during treatment in emotional reactivity will mediate changes in PTSD symptoms.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Risk Reduction through Family Therapy
  • Behavioral: Treatment as Usual
N/A

Detailed Description

See above.

Study Design

Study Type:
Interventional
Actual Enrollment :
135 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Integrative Risk Reduction and Treatment for Teen Substance Use Problems and PTSD
Actual Study Start Date :
Nov 1, 2012
Actual Primary Completion Date :
Jul 12, 2018
Actual Study Completion Date :
Jul 12, 2018

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Treatment as Usual (TAU)

Treatment as Usual (TAU) will be defined as it already exists within the community child advocacy centers. This could include individual and/or group therapy using a variety of treatment models.

Behavioral: Treatment as Usual
Participants assigned to the TAU condition will receive the standard treatment that a CSA victim would typically receive at community advocacy centers. In addition to treatment that is typically offered at the CACs, this will include a referral for substance abuse evaluation and may include referrals to other agencies in the community. TAU has been utilized as a comparison condition for several behavioral treatment evaluations involving adolescent substance abuse.
Other Names:
  • TAU
  • Experimental: RRFT

    RRFT is an acronym for an experimental intervention named Risk Reduction through Family Therapy. Please see intervention description for more detail about the model.

    Behavioral: Risk Reduction through Family Therapy
    RRFT is an integrative, ecologically-based approach to risk reduction and treatment. A Stage 1a feasibility trial and a Stage 1b pilot randomized controlled trial (RCT) evaluating RRFT have been completed. This Stage 1 work has resulted in a treatment manual, a clinician training protocol, and a quality assurance system. Preliminary findings from these studies are promising, indicating that RRFT can be readily learned and implemented with fidelity, and that it can lead to improvements in drug use and drug use-related risk and protective factors, PTSD symptoms, and risky sexual behaviors.
    Other Names:
  • RRFT
  • Outcome Measures

    Primary Outcome Measures

    1. change in substance use problems (initiation/continuation, quantity, and abuse symptoms) [18 months]

    Secondary Outcome Measures

    1. change in PTSD severity and symptoms [18 months]

    2. change in risky sexual behaviors [18 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    13 Years to 18 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
      1. 13-18 years old;
      1. Presenting to LCC/HH for evaluation or treatment;
      1. Report having experienced IPV in their lifetime, including: CSA, defined as forced or unwanted: (a) vaginal or anal penetration by an object, finger, or penis; (b) oral sex; (c) touching of the respondent's breasts or genitalia; or (d) respondents' touching of another person's genitalia; CPA, defined as having been (a) attacked or threatened with a gun, knife, or some other weapon; (b) attacked by another person with perceived intent to kill or seriously injure; (c) beaten and injured (i.e., "hurt pretty badly") by another person; (d) spanked so forcefully that it resulted in sustained welts or bruises or required medical care; or (e) cut, burned, or tied up by a caregiver as a punitive consequence; Exposure to Domestic Violence; and being victim of or bearing witness to Community Violence.
      1. Have a memory of the incident(s);
      1. Five or more DSM-IV PTSD symptoms;
      1. Substance use, defined as alcohol or illicit drug use in the past 90 days per self-report and/or urine drug screen or breathalyzer.
    Exclusion Criteria:
      1. Previously identified as having a Pervasive Developmental Disability or Moderate to Severe Mental Retardation;
      1. Actively suicidal or homicidal;
      1. Reports active psychotic disorder

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Medical University of South Carolina Charleston South Carolina United States 29425

    Sponsors and Collaborators

    • Medical University of South Carolina
    • National Institute on Drug Abuse (NIDA)

    Investigators

    • Principal Investigator: Carla K Danielson, PhD, Medical University of South Carolina

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Medical University of South Carolina
    ClinicalTrials.gov Identifier:
    NCT01751035
    Other Study ID Numbers:
    • Pro00009042
    • R01DA031285-01
    First Posted:
    Dec 17, 2012
    Last Update Posted:
    Aug 3, 2018
    Last Verified:
    Aug 1, 2018
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 3, 2018