View Clinical Trial (Medical Research Study)
Effects of Contingency Management for Methamphetamine Abstinence on Post-Exposure Prophylaxis for HIV in Men Who Have Sex With Men (MSM) - NCT00856323-90028(Clinical Trial 276005)
ClinicalConnection.com has recently undergone an update and this page may no longer be up-to-date. Please Search For Clinical Trials to view the most current clinical trials listings.
| City: |
|
Los Angeles |
|
State:
|
|
CA |
| Zip Code: |
|
90028 |
| Conditions: |
|
Amphetamine-Related Disorders - HIV - HIV Infections |
| Purpose: |
|
This study seeks to decrease methamphetamine use and concomitant high-risk sexual behaviors
among methamphetamine-using men who have sex with men (MSM) by combining a biomedical
intervention with a behavioral intervention. The behavioral intervention will consist of an
8-week course of contingency management (CM) through which participants will be reinforced
for testing negative for methamphetamine metabolites during periodic urine analyses. The
biomedical intervention involves a 28-day course of an antiretroviral drug (Truvada) to be
administered after an unanticipated HIV risk exposure (i.e., engaging in either receptive or
insertive anal sex without a condom with someone who is HIV-positive or of unknown status).
In combining these two interventions, this study seeks to evaluate the combined
intervention's effects on sexual risk behaviors and methamphetamine use.
|
| Study summary: |
|
|
| Criteria: |
|
Inclusion Criteria:
- Individual must identify as a male who has sex with other men (MSM);
- At least 18 years of age;
- HIV negative serostatus on baseline rapid oral HIV antibody test;
- Self-reported methamphetamine use within the previous 72 hours and test positive for
methamphetamine metabolites at baseline;
- Self-reported unprotected anal intercourse (either receptive or insertive) with an
HIV-positive or status unknown partner within the previous 3 months;
- Self-reports no previous hypersensitivity to any of the components of Truvada
(tenofovir disoproxil fumarate or emtricitabine);
- Willing to comply with study requirements (i.e., monitored urine testing three times
per week, meet with physician within first week of enrollment, begin medication
immediately following an unexpected high-risk sexual exposure, and contact the clinic
and meet with physician within 92 hours of unexpected high-risk sexual exposure).
Exclusion Criteria:
- Does not identify as a male who has sex with other men;
- Under 18 years of age;
- HIV positive, by self-report or as indicated by the results on the baseline rapid
oral HIV antibody test;
- Self-reports any previous hypersensitivity to any of the components of Truvada;
- Has not used methamphetamine in the previous 72 hours and does not test positive for
methamphetamine metabolites;
- Has not had unprotected anal intercourse with an HIV-positive or status unknown
partner within the previous 3 months;
- Unwilling to comply with study requirements. |
|
|
|
|
|
|
|
|
If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
|
| Trials Alerts: |
|
If you would like to be
notified of new clinical trials as they become available please
register for a free account.
|
|
| Data Source: |
|
ClinicalTrials.gov |
| Date Processed: |
|
February 17, 2011 |
Modifications to
this listing: |
|
Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
|
|
|
|
|
|
|
|