Actively Recruiting
Implementing HIV Pre-Exposure Prophylaxis in a Family Planning Clinic: A Study of Feasibility and Acceptability (The Pilot Fish Study)
Led by Women and Infants Hospital of Rhode Island · Updated on 2026-05-29
83
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
W
Women and Infants Hospital of Rhode Island
Lead Sponsor
A
Advance RI CTR
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating how patients and physicians feel about offering medications called pre-exposure prophylaxis (PrEP) to prevent HIV in a family planning clinic. The study focuses on whether patients find it acceptable to be asked about PrEP during their clinic visits, as well as understanding the challenges and supports for discussing and starting PrEP in this setting. The study aims to provide data to help design better ways to offer PrEP in family planning clinics. The study offers standardized counseling about PrEP to patients and provides an opportunity to begin PrEP as part of routine care. Physicians receive training on a standardized PrEP screening and initiation protocol and support patients interested in starting PrEP. There is no control group; this is a pilot study to assess feasibility and acceptability of integrating PrEP into family planning services. Participants will complete surveys about their experiences with PrEP screening and initiation. Patients complete a post-intervention survey and receive a gift card, while physicians complete pre- and post-study surveys and some may take part in in-depth interviews. Researchers measure how acceptable, feasible, and appropriate the intervention is for both patients and physicians during the study period, which lasts up to 12 months for physicians and up to 6 hours for patients.
CONDITIONS
Brief Title
Bringing Medicines for HIV Prevention to a Family Planning Clinic
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 16 or older
- Presenting for care at the Women and Infants Hospital of Rhode Island Family Planning Clinic
- Able to speak English or Spanish
- Have decisional capacity
You will not qualify if you...
- Currently seeking abortion care
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person)
Duration - Up to 6 hours for patient participants; Up to 12 months for physician participants
Participants complete surveys and provide feedback on the acceptability and feasibility of the PrEP screening and initiation procedures.
1 or more survey visits depending on participant role
Trial Site Locations
Total: 1 location
1
Women and Infants Hospital of Rhode Island
Providence, Rhode Island, United States, 02905
Actively Recruiting
Research Team
B
Benjamin P Brown, MD, MS
E
Erica J Hardy, MD, MMSc, MA
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
SCREENING
Number of Arms
2
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