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Clinical Trial Summary

This multi-site randomized controlled trial enrolling sexual minority men who use stimulants and are currently taking pre-exposure prophylaxis (PrEP). This randomized controlled trial will test the efficacy of a PrEP Affect Regulation Treatment Innovation (PARTI) condition comprised of a 5-session positive affect intervention delivered during smartphone-based Contingency Management (CM) for directly observed PrEP doses (PARTI+CM) compared to an attention-control condition delivered during CM. The primary outcome is HIV acquisition risk measured using a combination of tenofovir-diphosphate levels in dried blood spots that are indicative of sub-optimal adherence to PrEP and recent condomless anal sex.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04899024
Study type Interventional
Source Florida International University
Contact Adam W. Carrico, PhD
Phone 305-348-7887
Email acarrico@fiu.edu
Status Recruiting
Phase N/A
Start date January 31, 2022
Completion date July 1, 2026

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