HIV/AIDS Clinical Trial
Official title:
HIV Incidence in a Cohort of and Evaluation of Pre-Exposure Prophylaxis for High Risk Adolescent Girls and Young Women in Urban Lilongwe, Central Malawi
To provide preliminary evidence about feasibility and acceptability of delivering PrEP to AGYW identified as potentially at high risk of HIV infection in Lilongwe city communities and two public facilities in Lilongwe, Malawi. The primary objective of the study is to assess the feasibility, acceptability, tolerability and cost of delivering PrEP among high-risk AGYW aged 18-24 years and healthcare providers in urban Lilongwe. Secondary objectives are (i) to assess the program's ability to enroll and retain a PrEP cohort for one year and (ii) measure the incidence of HIV infection among high risk AGYW in urban Lilongwe among women who decline to enroll in the PrEP study (these will be offered enrollment in the HIV incidence study).
The main goal of the study is to provide preliminary evidence about feasibility and
acceptability of delivering PrEP to AGYW identified as potentially at high risk of HIV
infection in Lilongwe city communities and two public facilities in Lilongwe, Malawi. The
primary objectives are to; determine HIV prevalence among all AGYW identified as potentially
at high risk of HIV infection in urban Lilongwe; assess the HIV program's ability to enroll
and retain the PrEP cohort for one year; assess participants' and providers' perceptions of
the barriers and facilitators for providing PrEP to inform implementation of PrEP study and
future interventions and assess the cost of PrEP delivery in the routine HIV program.
Secondary Objectives:
1. To measure annual HIV incidence in a prospective cohort of HIV-negative AGYW identified
as potentially at high risk of HIV infection but declined to enroll in PrEP cohort study
in urban Lilongwe.
2. To measure annual HIV incidence among HIV-negative AGYW who enrolled in PrEP cohort
study in urban Lilongwe.
3. To determine risk factors for HIV in a cohort of AGYW recruited in the prospective
cohort study
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