Fact CheckerSign in

NCT06746675Not yet recruiting

Evaluating the Healthy Families PrEP Program for Women at Risk for HIV

Evaluating Healthy Families PrEP: an Intervention to Promote PrEP Use During Periconception, Pregnancy and Postpartum Periods for Women in Rural Uganda

Source: ClinicalTrials.gov · Last updated 26 Oct 2026

Brief summary (registry, in English)

Study investigators developed and piloted a counselling intervention, Healthy Families-PrEP, that supports women to use HIV prevention strategies while trying for and during pregnancy. They will now adapt the intervention to community clinics and postpartum women and test the intervention. The goal is to reduce HIV incidence among women and children.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
660 (estimated)
First submitted
18 Dec 2024
Start date
Dec 2026
Primary completion date
Jan 2031
Lead sponsor
Yale University
Diseases
HIV
NCT number
NCT06746675

What you commit to

  • Study type: Interventional
  • Planned participants: 660
  • From Dec 2026 to the primary completion date, Jan 2031
  • 1 site in 1 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 illness

  • HIV-positive (onsite rapid testing)

Other

  • Not reporting pregnancy in the past 2 years
  • Does not report personal or partner desire to have a child in the next year
  • Not willing to provide informed consent
  • Not able to communicate in English or local language
  • Does not report pregnancy in the past 2 years and/or does not report personal or partner desire to have a child in the next year
  • Not able to communicate in English or local language
  • Living beyond 60km of the trial healthcare center

Who the study is looking for

  • Age ≥18 years and ≤45 years
  • Willing and able to participate in the informed consent process
  • HIV-uninfected by self-report, but have indications for HIV prevention strategies, such as having a partner living with HIV or who they think may be living with HIV
  • Reporting pregnancy in the past 2 years, and/or desire to have a child in the next year, and/or have a partner who desires to a child in the next year
  • Fluent in English or local language
  • Living within 60km of a healthcare center included in the trial
  • HIV Negative (onsite rapid testing)

Age in the registry: 18 years to 45 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mbarara University of Science and Technology
Coordinator of this site? Confirm its status
MbararaUgandaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.