Integrating PrEP Decision Making Into Counseling in Sexual and Reproductive Health Clinics
Recruiting · NCT06684613 · Interventional (participants receive a specific treatment) · Lead sponsor: Yale University
View the official record on ClinicalTrials.gov →Interventions studied
Generic InformationPrEP Decision Aid
What this trial is about
This study addresses the need for HIV prevention to be integrated into counseling visits at sexual and reproductive health clinics.
Who can take part
Age range
18 Years and older
Sex
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)
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 .
Where it is running
1 location listed across 1 US state.
- Yale Clinical and Community Research - New Haven, Connecticut, United States