Actively Recruiting

Phase Not Applicable
Age: 16Years +
All Genders
Healthy Volunteers
ID06930508

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

Age: 16Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • Currently seeking abortion care

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit (in-person)

Surveillance

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

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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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