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Integrating PrEP Decision Making Into Counseling in Sexual and Reproductive Health Clinics
RecruitingPhase 2Healthy volunteers welcome
Project Carmenta: Integrating PrEP Decision Making Into Counseling in Sexual and Reproductive Health Clinics
Who can join
Ages 18 and older · Women · Healthy volunteers welcome
Full eligibility criteria
Patients (inclusion): * Woman * Aged 18 years or older * Have a uterus * Do not have HIV (by self-report) * Not currently on PrEP * Comfortable conversing in English or Spanish * Able to participate in informed consent procedures Patients (exclusion): * People who cannot become pregnant (i.e., have had a hysterectomy or tubal ligation) * People who wish to become pregnant (will not qualify for pregnancy prevention counseling) * Have a scheduled visit with a member of the investigative team (to minimize risk of potential ascertainment bias) * Participants of Aim 1 cannot participate in Aim 2. Sexual and Reproductive Health clinicians will be included if they provide sexual and reproductive health patient care at any of the participating sites. Clinic staff will be included if they work at any of the participating sites and have patient-facing or non-patient-facing roles .
About the study
This study addresses the need for HIV prevention to be integrated into counseling visits at sexual and reproductive health clinics.
What is being tested
- PrEP Decision Aid (device)
- Generic Information (other)
Sponsor: Yale University · Participants: 50 · Started: Mar 11, 2026
Contact the study team
- Carolina Price, MPA · Phone: 2034998075
- Jaimie P Meyer, MD · Phone: 2037376233
Official record on ClinicalTrials.gov — NCT06684613
Locations in the U.S.
| Connecticut | Yale Clinical and Community Research, New Haven |
From ClinicalTrials.gov, data retrieved Oct 1, 2026. Each study sets its own eligibility; the study team decides who can join.