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Clinical Trials/NCT03642314
NCT03642314
Unknown
Not Applicable

ImPrEP Sub-study - HIV Self-Testing to Increase Combination Prevention Demand in the ImPrEP Project: an Adaptative Randomized Trial

Oswaldo Cruz Foundation0 sites876 target enrollmentSeptember 2018
ConditionsHIV Prevention

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HIV Prevention
Sponsor
Oswaldo Cruz Foundation
Enrollment
876
Primary Endpoint
voucher redemption proportion by arm
Last Updated
7 years ago

Overview

Brief Summary

This is a sub-study of an ongoing PrEP study ( HIV PrEP for men who have sex with men - MSM - and transgender women - TGW: a demonstrative project in Brazil, Peru and Mexico - ImPrEP). MSM/TGW enrolled to ImPrEP Study at the selected sites, who agree to participate in this HIV Self Test (HIVST) sub-study, will be 1:1 randomized at the third study visit either to receive 5 HIVST+voucher (intervention arm) or 5 vouchers alone (control arm) to secondarily distribute into their MSM/TGW network. All vouchers are numbered invitations for priority access to individualized HIV risk assessment and combination prevention services, including PrEP, at the ImPrEP sites. Study population comprises ImPrEP participants and their referred peers. Sample size is going to be determined at an interim analysis performed when each city has enrolled 70 participants. Trial participants will be at maximum 876 (438 intervention and 438 in the control arm) MSM and TGW included in the ImPrEP Study who received PrEP for at least 6 months in the sites from Rio de Janeiro and Lima. The study is designed as a multicenter, open, adaptative, randomized trial. The main study outcome is the voucher redemption proportion by arm.

Registry
clinicaltrials.gov
Start Date
September 2018
End Date
September 2022
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Oswaldo Cruz Foundation
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • individuals who were included in the ImPrEP Study
  • performed at least 3 study visits,
  • accepted to participate in this sub study,
  • provide informed consent form

Exclusion Criteria

  • Individuals included into ImPrEP as a result of HIVST secondary distribution

Outcomes

Primary Outcomes

voucher redemption proportion by arm

Time Frame: 2 years

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