Motivational Enhancement to Improve Treatment Engagement and Outcome in Subjects Seeking Treatment for Substance Abuse - 1

NCT ID: NCT00032981

Last Updated: 2017-01-12

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

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

561 participants

Study Classification

INTERVENTIONAL

Study Start Date

2001-05-31

Study Completion Date

2004-08-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Substance-Related Disorders

Study Design

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Allocation Method

RANDOMIZED

Primary Study Purpose

TREATMENT

Interventions

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Behavior Therapy

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Yale University

OTHER

Sponsor Role lead

Responsible Party

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Yale University School of Medicine

Principal Investigators

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Kathleen Carroll, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

VA Connecticut Healthcare System

Locations

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Haight Ashbury Free Clinics

San Francisco, California, United States

Site Status

Tarzana Treatment Center

Tarzana, California, United States

Site Status

CT Renaissance, Inc.

Norwalk, Connecticut, United States

Site Status

LMG Programs, Inc.

Stamford, Connecticut, United States

Site Status

Rehab After Work

Philadelphia, Pennsylvania, United States

Site Status

Northeast Treatment Center

Philadelphia, Pennsylvania, United States

Site Status

Countries

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United States

Related Links

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Other Identifiers

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NIDA-CTN-0004-1

Identifier Type: -

Identifier Source: org_study_id

NCT00016770

Identifier Type: -

Identifier Source: nct_alias

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