NCT06335121Not yet recruiting
Implementation of PrEP Care Among Women in Family Planning Clinics
Source: ClinicalTrials.gov · Last updated 22 Jan 2026
Brief summary (registry, in English)
This study will evaluate implementation strategies to address barriers and increase uptake of PrEP among Black cisgender women in Planned Parenthood of Illinois (PPIL) health centers.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 250 (estimated)
- First submitted
- 21 Mar 2024
- Start date
- 1 Dec 2026
- Primary completion date
- 30 Jun 2027
- Lead sponsor
- Rush University Medical Center
- Diseases
- HIV
- NCT number
- NCT06335121
What you commit to
- Study type: Interventional
- Planned participants: 250
- From 1 Dec 2026 to the primary completion date, 30 Jun 2027
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- \- Participants will be excluded if they are not PrEP eligible, have a negative STI test, or are not identified in the EHR.
Who the study is looking for
- Eligible participants include ciswomen presenting at a PPIL health center with a positive STI test (syphilis, gonorrhea, or chlamydia) and identified in the EHR using STI testing records and new fields for optimizing support of provider PrEP counseling.
Age in the registry: 18 years to 45 years · Sex: Female · Accepts healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.