The Test-to-PrEP Study
Recruiting · NCT06927856 · Interventional (participants receive a specific treatment) · Lead sponsor: University of Miami
View the official record on ClinicalTrials.gov →Interventions studied
Access by ReferralTest-to-PrEP
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.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- PrEP Clients (Egos):
- Stated willingness to provide informed consent.
- Stated willingness to comply with all study procedures.
- Stated availability for the duration of the study.
- Ability to identify members of their social network who may benefit from receiving an HIVST kit and PrEP information.
- Currently prescribed PrEP by RAPID clinics, including those initiating PrEP on the same day as study enrollment.
- Inclusion Criteria for Peers (Alters):
- \- Provision of electronic informed consent prior to completion of the Quick Response (QR)-linked survey instruments.
Exclusion criteria
- for PrEP Clients (Egos):
- Inability or refusal to provide informed consent (e.g., cognitive impairment).
- Unable or unwilling to comply with study procedures per study investigator
- Inability to identify members of their social network who may benefit from receiving an HIVST kit and PrEP information.
- Aged 17 years or younger.
- Exclusion Criteria for Peers (Alters):
- Failure to provide electronic informed consent prior to starting QR-linked Alter survey tools.
- Age 17 years or younger.
Where it is running
1 location listed across 1 US state.
- University of Miami - Miami, Florida, United States