Child Behavior Disorders |
Bullying |
Clinical Trial: Motivational Enhancement to Improve Treatment Engagement and Outcome in Subjects Seeking Treatment for Substance Abuse - 1
This study is no longer recruiting patients.
Purpose
The purpose of this study is to evaluate the therapeutic usefulness of incorporating Motivational Enhancement Treatment into the standard drug abuse treatment entry process of Community Treatment Programs on improving treatment engagement, retention, and outcome.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Substance-Related Disorders | Behavior: Behavior Therapy | Phase III |
MedlinePlus related topics: Drug Abuse; Prescription Drug Abuse
Study Type: Interventional
Study Design: Treatment, Randomized, Uncontrolled
Official Title: Motivational Enhancement Treatment (MET) to Improve Treatment Engagement and Outcome in Subjects Seeking Treatment for Substance Abuse
Expected Total Enrollment: 561
Study start: August 2000
Participants seeking treatment at the participating CTPs will be randomly assigned to either "standard" or "MET/MI" treatment, with a 1- and 3-month follow-up. Primary outcome measures will include (1) treatment retention (e.g., number of sessions/weeks completed, the rate of patients completing 3 or more subsequent sessions, and (2) substance use (e.g., urinalyses, days of opioid, cocaine, marijuana, alcohol use, rates of abstinence). Secondary outcomes will include motivation, psychosocial functioning, HIV risk behaviors, treatment utilization, and patient satisfaction. Process assessments will include measures of the working alliance as well as therapist adherence/competence ratings which will evaluate how effectively MET/MI was implemented. Participating CTPs will implement one of two independent protocols, depending on which is the best suited or feasible for the intake procedures at their clinic. Thus, following an invitation to participate, explanation of the study, and provision of informed consent, patients would complete a brief assessment battery followed by either: 1) Random assignment to 3 individual sessions of standard treatment (treatment as usual) at the program versus 3 individual sessions of MET. or 2) Random assignment to 1 individual standard assessment/evaluation session.
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
Individuals will be eligible for the protocol who:
- Are seeking outpatient treatment for any substance use disorder
- Are willing to participate in the protocol (e.g., to be randomized to treatment, be contacted for follow-up assessment, to have their sessions audiotaped)
- Are able to understand and provide written informed consent
Exclusion Criteria:
Individuals will be excluded who:
- Are not sufficiently medically or psychiatrically stable to participate in outpatient treatment
- Are seeking detoxification only, methadone maintenance treatment or residential inpatient treatment
Location Information
California
Haight Ashbury Free Clinics, San Francisco, California, 94117, United States
Tarzana Treatment Center, Tarzana, California, 91356, United States
Connecticut
LMG Programs, Inc., Stamford, Connecticut, 06901, United States
CT Renaissance, Inc., Norwalk, Connecticut, 06852, United States
Pennsylvania
Rehab After Work, Philadelphia, Pennsylvania, 19103, United States
Northeast Treatment Center, Philadelphia, Pennsylvania, 19123, United States
Kathleen Carroll, Ph.D., Principal Investigator, VA Connecticut Healthcare System
More Information
Record last reviewed: August 2004
Last Updated: February 16, 2005
Record first received: April 5, 2002
ClinicalTrials.gov Identifier: NCT00032981
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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