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Study identifier: NCT06558825 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Pre-exposure Prophylaxis (PrEP) Uptake and Adherence Intervention for Women with Trauma-related Conditions

Condition: Substance Use  ·  Sponsor: The University of Texas Health Science Center, Houston

PhaseNA
Planned participants60
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

The investigators have previously developed an integrated bio-behavioral intervention to promote PrEP uptake and adherence in cisgender women who are undergoing treatment for trauma-related mental health conditions and who are at a higher risk for HIV. The intervention is delivered within the mental health treatment setting and integrates knowledge, behavioral skills, and motivation to engage in and adhere to PrEP care. The purpose of this study is to assess the preliminary efficacy, feasibility, and acceptability of this intervention. The hypothesis is that, compared to standard treatment, the intervention will be feasible, acceptable, and associated with greater PrEP uptake and adherence.

This description comes directly from the study's public registry record.

Talk to the study team

Angela M 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.

Locations (1)

Louis A. Faillace, MD, Department of Psychiatry and Behavioral Sciences, University of Texas Health Science Center at HoustonHouston, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06558825