Integrating PrEP Decision Making Into Counseling in Sexual and Reproductive Health Clinics
Recruiting
N/AInterventional Study
Sexual Risk Behavior for HIV-infectionReproductive Health
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Prevention
Participants needed
50 (estimated)
Sponsor
Yale University · Other
Who this trial is looking for
This trial is looking for women aged 18 and older with a uterus who want to help improve HIV prevention counseling in clinics. Participants will discuss their experiences and help test new counseling approaches.
Are You a Good Fit for This Trial?
You may be able to join if
I am a woman
I am 18 years or older
I have a uterus
I do not have HIV
I am not currently on PrEP
I can speak English or Spanish
I can agree to participate in this trial
You may not be able to join if
I cannot become pregnant
I wish to become pregnant
I have a visit scheduled with someone from the study team
I am participating in another part of the study
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
This study addresses the need for HIV prevention to be integrated into counseling visits at sexual and reproductive health clinics.
Trial Locations
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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., ha…
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 .
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