Behavioral Therapy Development for Methamphetamine Abusers
This study has suspended participant recruitment.
Sponsor:
University of California, Los Angeles
Collaborator:
Information provided by (Responsible Party):
Steve Shoptaw, University of California, Los Angeles
ClinicalTrials.gov Identifier:
NCT00249678
First received: November 3, 2005
Last updated: May 31, 2013
Last verified: May 2013
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
The Study Was Designed to Develop a Cognitive Behavioral Approach to Treating Methamphetamine Abuse in HIV Primary Care Settings. |
Behavioral: Behavior Therapy |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Primary Purpose: Treatment |
| Official Title: | Behavioral Therapy Development for Methamphetamine Abuse |
Resource links provided by NLM:
Further study details as provided by University of California, Los Angeles:
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Criteria
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.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00249678
Locations
| United States, California | |
| UCLA CARE Clinic | |
| Los Angeles, California, United States, 90035 | |
| UCLA Medical Center | |
| Los Angeles, California, United States, 90024 | |
| UCLA, Integrated Substance Abuse Programs | |
| Los Angeles, California, United States, 90024 | |
Sponsors and Collaborators
University of California, Los Angeles
Investigators
| Principal Investigator: | James Peck, Other | University of California, Los Angeles |
More Information
No publications provided
| Responsible Party: | Steve Shoptaw, Professor, University of California, Los Angeles |
| ClinicalTrials.gov Identifier: | NCT00249678 History of Changes |
| Other Study ID Numbers: | NIDA-18075-1, R21DA018075, R21-18075-1 |
| Study First Received: | November 3, 2005 |
| Last Updated: | May 31, 2013 |
| Health Authority: | United States: Federal Government |
Keywords provided by University of California, Los Angeles:
|
Behavior Therapy methamphetamine |
Additional relevant MeSH terms:
|
Methamphetamine Sympathomimetics Autonomic Agents Peripheral Nervous System Agents Physiological Effects of Drugs Pharmacologic Actions Dopamine Agents Neurotransmitter Agents |
Molecular Mechanisms of Pharmacological Action Central Nervous System Stimulants Central Nervous System Agents Therapeutic Uses Adrenergic Agents Adrenergic Uptake Inhibitors Neurotransmitter Uptake Inhibitors Dopamine Uptake Inhibitors |
ClinicalTrials.gov processed this record on June 17, 2013