Condition: Substance Use · Sponsor: The University of Texas Health Science Center, Houston
The goal of this clinical trial is to test an addiction-clinic based behavioral intervention for increasing PrEP uptake and adherence among women who engage in high-risk sexual behaviors and problematic substance use. The main question it aims to answer is: • If the integrated intervention increase PrEP uptake and adherence compared to standard treatment Participants will * receive provision of PrEP information through 4 counseling sessions * prevention navigation * receive nurse practitioner prescribed PrEP in an addiction treatment setting Researchers will compare intervention group with standard treatment to see if the integrated intervention help increase PrEP uptake and adherence
This description comes directly from the study's public registry record.
Angela Heads, PhD · (713) 486-2830 · Angela.M.Heads@uth.tmc.edu
Kaixuan An · (713) 486-2531 · Kaixuan.An@uth.tmc.edu
Always discuss trial participation with your own doctor first.
| Louis A. Faillace, MD, Department of Psychiatry and Behavioral Sciences, University of Texas Health Science Center at Houston | Houston, Texas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06158607