- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00249678
Behavioral Therapy Development for Methamphetamine Abusers
February 13, 2020 updated by: Steve Shoptaw, University of California, Los Angeles
Behavioral Therapy Development for Methamphetamine Abuse
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.
Study Overview
Status
Withdrawn
Intervention / Treatment
Study Type
Interventional
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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California
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Los Angeles, California, United States, 90024
- UCLA Medical Center
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Los Angeles, California, United States, 90035
- UCLA CARE Clinic
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Los Angeles, California, United States, 90024
- UCLA, Integrated Substance Abuse Programs
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- 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
- Willing to give informed consent and comply with study procedures;
- Willing to provide consent to contact treating physicians and pharmacies to assess adherence to HIV medications;
- Diagnosed with current methamphetamine abuse as determined by MINI; and
- Interested in seeking treatment for their methamphetamine abuse and in participating in this research project.
Exclusion Criteria:
- Unwilling to give, or withdrawal of, informed consent;
- Inability to understand nature of study;
- 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);
- Current suicidal ideation or suicide attempt within the past 3 months; and
- Concurrent dependence on opiates, alcohol, or benzodiazepines as determined by MINI.
- Total lack of any type of healthcare coverage. These potential participants will be given low-fee treatment referrals.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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Craving
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Medication compliance
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Addiction severity
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Psychiatric interview
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Sex-risk behavior
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Secondary Outcome Measures
Outcome Measure |
|---|
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Depression
|
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Quality of Life
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: James Peck, Other, University of California, Los Angeles
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
September 1, 2004
Primary Completion (Actual)
May 1, 2007
Study Completion (Actual)
May 1, 2007
Study Registration Dates
First Submitted
November 3, 2005
First Submitted That Met QC Criteria
November 3, 2005
First Posted (Estimate)
November 7, 2005
Study Record Updates
Last Update Posted (Actual)
February 17, 2020
Last Update Submitted That Met QC Criteria
February 13, 2020
Last Verified
February 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- NIDA-18075-1
- R21DA018075 (U.S. NIH Grant/Contract)
- R21-18075-1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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