Behavioral Therapy Development for Methamphetamine Abusers

NCT ID: NCT00249678

Last Updated: 2020-02-17

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

WITHDRAWN

Clinical Phase

PHASE2

Study Classification

INTERVENTIONAL

Study Start Date

2004-09-30

Study Completion Date

2007-05-31

Brief Summary

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The purpose of this study is...to assess whether placing a substance abuse intervention for HIV+ methamphetamine users within an HIV medical care setting improves rates of follow-up on referral to treatment by primary care physicians; reduces drug use and sexual risk behaviors more than treatment-as-usual; and increases rates of adherence to HIV medication regimens.

Detailed Description

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Conditions

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The Study Was Designed to Develop a Cognitive Behavioral Approach to Treating Methamphetamine Abuse in HIV Primary Care Settings

Study Design

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Primary Study Purpose

TREATMENT

Interventions

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Behavior Therapy

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. HIV-seropositive, GBM receiving medical treatment for HIV for at least 30 days prior to signing informed consent at the UCLA CARE clinic, aged 18-65
2. Willing to give informed consent and comply with study procedures;
3. Willing to provide consent to contact treating physicians and pharmacies to assess adherence to HIV medications;
4. Diagnosed with current methamphetamine abuse as determined by MINI; and
5. Interested in seeking treatment for their methamphetamine abuse and in participating in this research project.

Exclusion Criteria

1. Unwilling to give, or withdrawal of, informed consent;
2. Inability to understand nature of study;
3. A psychiatric condition that, in the principal investigator's judgment, warrants additional intervention to ensure participant safety (e.g., meets DSM-IV-TR criteria for current bipolar disorder or a psychotic disorder);
4. Current suicidal ideation or suicide attempt within the past 3 months; and
5. Concurrent dependence on opiates, alcohol, or benzodiazepines as determined by MINI.
6. Total lack of any type of healthcare coverage. These potential participants will be given low-fee treatment referrals.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role collaborator

University of California, Los Angeles

OTHER

Sponsor Role lead

Responsible Party

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Steve Shoptaw

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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James Peck, Other

Role: PRINCIPAL_INVESTIGATOR

University of California, Los Angeles

Locations

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UCLA Medical Center

Los Angeles, California, United States

Site Status

UCLA, Integrated Substance Abuse Programs

Los Angeles, California, United States

Site Status

UCLA CARE Clinic

Los Angeles, California, United States

Site Status

Countries

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United States

Other Identifiers

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R21DA018075

Identifier Type: NIH

Identifier Source: secondary_id

View Link

R21-18075-1

Identifier Type: -

Identifier Source: secondary_id

NIDA-18075-1

Identifier Type: -

Identifier Source: org_study_id

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