Feasibility of an Ingestible Sensor System to Measure PrEP Adherence in YMSM

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18-24
SponsorHektoen Institute for Medical Research

About this trial

The goal of this study is to evaluate an integrated technology system that confirms ingestion of oral PrEP, monitors adherence both in real-time and longitudinally, and provides visual feedback mechanisms to promote enhanced adherence behaviors.

Eligibility criteria

Qualifiers

PrEP-eligible YMSM

Ages 18-24

Biologically born male

Report interest in PrEP

Disqualifiers

HIV+

Creatinine clearance <60 cc/min)

Allergy to topical adhesive

Acute gastrointestinal symptoms

Trial design

Treatments tested in this trial

  • Proteus Sensor System

Treatment groups

100 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Hektoen Institute for Medical Research

Lead sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Collaborator