PrEP Readiness Interventions for Sustained Motivation (PRISM)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorFlorida International University

About this trial

This is a hybrid type I randomized controlled trial to test the effectiveness of contingency management (CM) alone versus CM with motivational interviewing (MI) for optimizing entry or re-entry into the HIV prevention or care continua. A total of 400 participants will be randomized to CM (n = 200) or MI+CM (n = 200), all delivered via telehealth. Monthly follow-up assessments will be completed over 12 months to examine effectiveness MI+CM for the primary outcome - filling a pre-exposure prophylaxis (PrEP) or anti-retroviral therapy (ART) prescription (verified using a digital photo). Secondary outcomes will include: self-reported PrEP or ART clinical evaluation by a provider; self-reported meth and other substance use severity (ASSIST), and self-reported receptive and insertive condomless anal sex (CAS).

Eligibility criteria

Qualifiers

18 years or older

Assigned male a birth

Self-reported methamphetamine use in the past 3 months

HIV-negative or unknown serostatus at baseline

Disqualifiers

Unwilling or unable to provide informed consent

Trial design

Treatments tested in this trial

  • Motivational Interviewing (MI)
  • Contingency Management (CM)

Treatment groups

400 Participants
are divided into 2 treatment groups