About this trial
This study evaluates strategies to improve access to HIV prevention through the integration of pre-exposure prophylaxis (PrEP) into existing healthcare settings, rather than limiting delivery to specialty clinics. The study addresses barriers to PrEP uptake, including limited awareness, stigma, and restricted access, and recognizes that availability alone may not ensure initiation or sustained use.
The study includes two components. First, a longitudinal cohort of current PrEP users will be followed to assess changes in access, preferences, and PrEP use over time in real-world settings. Second, a dynamic decision-support toolkit will be developed and evaluated to support patients and providers in PrEP-related decision-making. The toolkit will include patient- and provider-facing components to support clinical decision-making, improve risk understanding, and facilitate integration of PrEP into routine healthcare. The toolkit will be refined and beta-tested in selected healthcare facilities in Botswana and Alabama.
Eligibility criteria
Qualifiers
18 years of age or older
Currently using or eligible for PrEP
18 years of age or older
Participated in the parent Tshireletso study in Botswana
Disqualifiers
None
Trial design
Treatments tested in this trial
- Observational cohort (PrEP use in real-world settings)
Treatment groups
Locations
1Map coordinates are unavailable for these locations. Locations are shown below instead.
Sponsors and collaborators
University of Alabama at Birmingham
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborator
Beth Israel Deaconess Medical Center
Collaborator
Harvard School of Public Health (HSPH)
Collaborator