NCT06930508Recruiting
Bringing Medicines for HIV Prevention to a Family Planning Clinic
Implementing HIV Pre-Exposure Prophylaxis in a Family Planning Clinic: A Study of Feasibility and Acceptability (Aka The Pilot Fish Study)
Source: ClinicalTrials.gov · Last updated 6 Aug 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 83 (estimated)
- First submitted
- 1 Apr 2025
- Start date
- 28 May 2026
- Primary completion date
- 31 Oct 2026
- Lead sponsor
- Women and Infants Hospital of Rhode Island
- Diseases
- HIV
- NCT number
- NCT06930508
What you commit to
- Study type: Interventional
- Planned participants: 83
- From 28 May 2026 to the primary completion date, 31 Oct 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- 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
- This study will not have any specific exclusion criteria for physician participants.
Age in the registry: 16 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Women and Infants Hospital of Rhode Island Coordinator of this site? Confirm its status | Providence | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.