Actively Recruiting
PrEP My Way: A Hybrid Type 1 Clinical Effectiveness-implementation Trial to Promote PrEP Persistence Among Young Kenyan Women
Led by Massachusetts General Hospital · Updated on 2026-04-22
500
Participants Needed
1
Research Sites
195 weeks
Total Duration
On this page
Sponsors
M
Massachusetts General Hospital
Lead Sponsor
K
Kenya Medical Research Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
PrEP My Way is a novel PrEP delivery system consisting of clinic-based PrEP initiation, followed by peer-delivered kits for HIV self-testing, PrEP refills, vaginal swabs for gonorrhea and chlamydia self-sampling, pregnancy tests, and contraception refills, if desired. Based on Social Cognitive Theory, the overall hypothesis is that PrEP My Way will overcome critical stigma and structural barriers that currently limit PrEP use and thus empower young women to promote their sexual health. Preliminary testing of PrEP My Way in Kisumu, Kenya found it to be highly feasible and acceptable, but PrEP use as an oral medication was lower than expected. Now that newer PrEP formulations are becoming available, the team is adding choice of PrEP formulation (i.e., oral tenofovir/emtricitabine, injectable cabotegravir-long acting \[CAB-LA\], or dapivirine ring) as well as choice of adherence support from peers (e.g., SMS \[short message service\], routine check-ins and/or WhatsApp groups) to the intervention. The study team will then test the effectiveness of the augmented PrEP My Way intervention (with and without testing for gonorrhea and chlamydia due to cost concerns) on PrEP persistence in women with ongoing HIV prevention needs (i.e., self-reported desire for PrEP, self-reported HIV risk, condomless sex, and/or multiple sexual partners). The team will also track implementation, service, and client metrics per Proctor's framework and determine cost-effectiveness of the intervention
CONDITIONS
Official Title
PrEP My Way: A Hybrid Type 1 Clinical Effectiveness-implementation Trial to Promote PrEP Persistence Among Young Kenyan Women
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Young women aged 16 to 24 years
- Starting PrEP at the recruitment site with required safety assessments completed
- Living in Kisumu County
- Own a mobile phone
- Able to understand Kiswahili, DhoLuo, or English
You will not qualify if you...
- Unable to provide informed consent (e.g., due to intoxication)
AI-Screening
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Trial Site Locations
Total: 1 location
1
Kenya Medical Research Institute
Kisumu, Kenya
Actively Recruiting
Research Team
L
Lindsey Garrison, MPH
CONTACT
J
Jessica Haberer, MD, MS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
3
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