Leveraging Infant Visit PrEP INtegration & tasK Shifting to Improve Post-partum HIV Prevention in Malawi

Recruiting N/A Interventional Study
Breastfeeding HIV Prevention
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.
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At a Glance
Age
15 – 99
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
5,000 (estimated)
Sponsor
University of North Carolina, Chapel Hill · Other
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About This Trial
The goal of the Leveraging Infant Visit PrEP INtegration \& tasK Shifting to Improve Postpartum HIV Prevention in Malawi (LINK) study is to evaluate both the effectiveness of a postpartum prevention package ("LINK model") among post-partum women and its implementation into existing clinical care models in Lilongwe, Malawi. The main question the study seeks to answer is: Do women at clinics implem…
Trial Locations
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Eligibility Criteria
PrEP user cohort: PrEP user cohort includes all adolescent and adult women \>=15 years old who are on PrEP and breastfeeding, enrolled in PrEP at each of the participating 12 sites during the study follow-up period. PrEP provision and clinical management will be at the discretion of the non-study P…
Contacts

Rutstein E Sarah, MD, PhD

(919) 966-2537

srutstein@unc.edu

CONTACT