Design and Evaluate 12 Week Group Therapy Intervention for HIV+ Methamphetamine Users and Deliver It Within an HIV/AIDS Primary Care Setting. - 1
The recruitment status of this study is unknown because the information has not been verified recently.
Verified November 2005 by National Institute on Drug Abuse (NIDA).
Recruitment status was Not yet recruiting
Recruitment status was Not yet recruiting
Sponsor:
Collaborator:
University of California, Los Angeles
Information provided by:
National Institute on Drug Abuse (NIDA)
ClinicalTrials.gov Identifier:
NCT00249678
First received: November 3, 2005
Last updated: NA
Last verified: November 2005
History: No changes posted
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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 |
|---|---|---|
|
Behavior Therapy Methamphetamine |
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 National Institute on Drug Abuse (NIDA):
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 | Not yet recruiting |
| Los Angeles, California, United States, 90035 | |
| Contact: Ardis Moe 310-557-2273 | |
| UCLA Medical Center | Not yet recruiting |
| Los Angeles, California, United States, 90024 | |
| Contact: Ardis Moe 310-557-2273 | |
| UCLA, Integrated Substance Abuse Programs | Not yet recruiting |
| Los Angeles, California, United States, 90024 | |
| Contact: James Peck, Other 310-312-0500 jpeck@mednet.ucla.edu | |
Sponsors and Collaborators
University of California, Los Angeles
Investigators
| Principal Investigator: | James Peck, Other | University of California, Los Angeles |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00249678 History of Changes |
| Other Study ID Numbers: | NIDA-18075-1, R21-18075-1 |
| Study First Received: | November 3, 2005 |
| Last Updated: | November 3, 2005 |
| Health Authority: | United States: Federal Government/HHS/NIH/NIDA |
Additional relevant MeSH terms:
|
Methamphetamine Amphetamine 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 May 19, 2013