← Back to all trials
Not Yet Recruiting
NCT07725679
A Hybrid Effectiveness-Implementation Trial of Urine Point-of-Care Assay to Increase PrEP Adherence Among Women in Kenya
Conditions: PrEP Adherence Monitoring
Sex: Female
Ages: 18 Years – 29 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 400
Sponsor: University of Washington
Summary
The goal of this randomized trial study is to learn if drug-level feedback counseling works to improve oral PrEP adherence in adolescent girls and young women.
Researchers will compare urine TFV assay positivity between arms. All participants will attend visits on the same schedule, and receive the same SOC counseling for PrEP adherence. Participants in the intervention arm will additionally take POC urine TFV tests and receive drug-level feedback as part of that counseling.
Eligibility Criteria
Inclusion Criteria:
* HIV uninfected
* Received daily oral PrEP one month prior, with a negative result on a urine assay one-month post PrEP initiation
* Currently attending or willing to attend one of the study clinics for PrEP refills
* Interest in continuing on oral PrEP despite adherence challenges
* No known sero-discordant relationships
* Living in Kiambu County and not planning to relocate for the next year
Exclusion Criteria:
* Inadequate capacity to consent or complete planned study procedures
* Do not speak English or Kiswahili
* Test positive for HIV at screening
* Concomitant participation in another PrEP adherence support study
Source: ClinicalTrials.gov (NCT07725679). StuddyBuddy aggregates publicly available trial information.