Clinical Trial

I-CAN Uganda Effectiveness Trial

Study acronym: I-CAN
Not Yet Recruiting
View on ClinicalTrials.gov →
Summary
This is a cluster-randomized controlled trial to determine the effectiveness of the community-based "I-CAN" intervention to improve agency in contraceptive decision-making and use in rural Uganda. Lay women will be trained to serve as peer mentors to other women of reproductive age in the community, using their own lived experience to provide support and information about contraceptive choices. Villages will be randomized to either receive the intervention or not. A household survey will be conducted at baseline before implementation activities begin and 24 months later. Interviews will also be conducted with mentors, participants, male partners of participants and other stakeholders. Researchers will compare preference-aligned contraceptive use (primary outcome), contraceptive agency, contraceptive method satisfaction, preference-aligned fertility management, and use of self-injectable contraception in villages with and without the intervention to determine effectiveness.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-07-13.
Trial Details
NCT Number NCT07711717
Lead Sponsor University of California, San Francisco
Collaborators: Makerere University, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Baitambogwe Community Healthcare Initiative (BACHI), AIDS Information Centre - Uganda (AIC)
Conditions Contraception
Enrollment 1,560 participants
Start Date 2026-10-13
Primary Completion 2028-12-31 (estimated)
Study Completion 2028-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-07-23