Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06927856

The Test-to-PrEP Study

Led by University of Miami · Updated on 2026-04-27

320

Participants Needed

1

Research Sites

168 weeks

Total Duration

On this page

Sponsors

U

University of Miami

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

To compare the effectiveness of two social network strategies (direct distribution and referral-based distribution) in increasing HIV self-testing (HIVST) completion rates among social network contacts of current Pre-Exposure Prophylaxis (PrEP) clients.

CONDITIONS

Official Title

The Test-to-PrEP Study

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Willingness to provide informed consent
  • Willingness to comply with all study procedures
  • Availability for the duration of the study
  • Ability to identify social network members who may benefit from receiving an HIV self-test kit and PrEP information
  • Currently prescribed PrEP by RAPID clinics, including same-day PrEP initiations
  • Provision of electronic informed consent by social network contacts (Alters) before completing surveys
Not Eligible

You will not qualify if you...

  • Inability or refusal to provide informed consent (e.g., cognitive impairment)
  • Unable or unwilling to comply with study procedures as determined by investigators
  • Inability to identify social network members who may benefit from HIV self-test kits and PrEP information
  • Age 17 years or younger for both PrEP clients (Egos) and social network contacts (Alters)
  • Failure to provide electronic informed consent by Alters before starting survey tools

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Miami

Miami, Florida, United States, 33136

Actively Recruiting

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Research Team

S

Susanne Doblecki-Lewis, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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