HIV/AIDS
Conditions
Interventions
Universal arm
Targeted arm
Sponsors
National Institute of Health
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Age =15 years Pregnant at any gestational age Tuberculosis negative Plans to reside in area for at least one year postpartum Plans to receive postnatal and infant care at the study facility Not currently enrolled in any other studies.
Exclusion criteria
Exclusion criteria: HIV+ at time of enrollment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Maternal HIV Incidence | — |
Secondary
| Measure | Time frame |
|---|---|
| Appropriate PrEP Use. Scored 1 for high risk women using PrEP and low risk women not using PrEP; 0 for high risk women NOT on PrEP and low risk women using PrEP;PrEP Adherence and duration on PrEP through sequential dried blood spots and number of days on PrEP ;Infant birthweight, preterm birth, and growth curves. To compare infant outcomes in PrEP exposed infants vs. unexposed; ;To estimate the incremental cost-effectiveness of targeted PrEP compared to universal PrEP for women during pregnancy and in the postpartum period, per incident HIV infection and disability adjusted life year (DALY) averted. | — |
Countries
Kenya
Contacts
Public ContactNancy Ngumbau
Study coordinator
Outcome results
None listed