Bringing Medicines for HIV Prevention to a Family Planning Clinic

Recruiting · NCT06930508 · Interventional (participants receive a specific treatment) · Lead sponsor: Women and Infants Hospital of Rhode Island

View the official record on ClinicalTrials.gov →

HIV

Interventions studied

Patient participant screeningPhysician participant training

What this trial is about

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.

Who can take part

Age range

16 Years and older

Sex

All (male and female)

Healthy volunteers

Yes - healthy volunteers may be accepted

Phase

Not applicable (e.g. observational or device study)

Study type

Interventional (participants receive a specific treatment)

Eligibility criteria (as published)

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.

Where it is running

1 location listed across 1 US state.

Women and Infants Hospital of Rhode Island - Providence, Rhode Island, United States

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →