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Implementing HIV Pre-Exposure Prophylaxis in a Family Planning Clinic: A Study of Feasibility and Acceptability (Aka The Pilot Fish Study)

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to understand what patients and physicians think about providing medications to prevent HIV transmission to patients in a family planning clinic. These medications are known as pre-exposure prophylaxis, or PrEP. The main questions to answer are: 1. Do patients find it acceptable to be asked about, and offered, PrEP during their visit to a family planning clinic? 2. What things make it easier or harder to ask about PrEP in a family planning clinic setting? 3. What things make it easier or harder to begin PrEP in a family planning clinic setting? Patient participants: 1. Will receive standardized counseling about PrEP. 2. Will have the opportunity to begin PrEP as part of their routine, ongoing care. 3. Will be asked to complete a survey about their experiences. Physician participants: 1. Will receive standardized education about PrEP. 2. Will talk to patient participants about PrEP, and support patient participants who want to begin PrEP. 3. Will be asked to complete pre-and post-study surveys about their experiences. 4. May be asked to complete a post-study in-depth interview about their experiences.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 16
Healthy Volunteers: t
View:

⁃ This study will include patient participants who:

• Are age 16 or older

• Are presenting for care at the Women and Infants Hospital of Rhode Island Family Planning Clinic

• Speak English or Spanish

• Have decisional capacity

⁃ This study will exclude patient participants who:

⁃ \- Are currently seeking abortion care

⁃ This study will include physician participants who:

⁃ \- Provide care at the Women and Infants Hospital of Rhode Island Family Planning Clinic

Locations
United States
Rhode Island
Women and Infants Hospital of Rhode Island
RECRUITING
Providence
Contact Information
Primary
Benjamin P Brown, MD, MS
benjamin_brown@brown.edu
401-274-1122
Backup
Erica J Hardy, MD, MMSc, MA
erica_hardy@brown.edu
401-453-7950
Time Frame
Start Date: 2026-05-28
Estimated Completion Date: 2026-07-31
Participants
Target number of participants: 83
Treatments
Experimental: Patient Participant
Experimental: Physician Participant
Related Therapeutic Areas
Sponsors
Collaborators: Advance RI CTR
Leads: Women and Infants Hospital of Rhode Island

This content was sourced from clinicaltrials.gov