Skip to main content
Clinical Trials/NCT06908252
NCT06908252CompletedPhase 4

Integrating PrEP Into Mobile Addiction and Primary Care Services (MAPS)

Duke University1 site in 1 country7 target enrollmentStarted: September 17, 2025Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 4
Status
Completed
Sponsor
Enrollment
7
Locations
1
Primary Endpoint
Enrollment

Study Overview

Brief Summary

For this study the investigators aim to see if giving participants an oral HIV prevention medication on a medical van, is a good option of care for individuals who inject drugs and/or are sexually active and therefore at a higher risk of contracting HIV.

Detailed Description

The purpose of this study is to evaluate a pilot program that provides Pre-Exposure Prophylaxis (PrEP) for people who use drugs (PWUD) and are at risk for contracting HIV. Given the ongoing overdose crisis and the risk of HIV among PWUD, this study aims to assess weather offering oral PrEP on a Medical Mobile Unit (MMU) is a viable strategy for preventing HIV transmission in high-risk populations. The other goal of this study is to assess community perceptions of PrEP and perceived HIV risk among Syringe Service Program (SSP) clients visiting a MMU.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •18 years or older, active drug injection user and/or sexually active, referred from the Syringe Service Program

Exclusion Criteria

  • •positive HIV status

Arms & Interventions

PrEP

Experimental

All eligible participants will be given oral PrEP pills to reduce their risk for contracting HIV.

Intervention: Pre-Exposure Prophylaxis (PrEP) (Drug)

Outcomes

Primary Outcomes

Enrollment

Time Frame: Baseline

Number of participants utilizing medical mobile unit during study duration who are eligible for PrEP

Negative HIV Status

Time Frame: up to 3 months

Number of participants who remain HIV negative at 3 months (Measured via negative HIV test at 3 months

PrEP Consultation

Time Frame: up to 6 months

Number of participants who agree to PrEP consultation

PrEP Initiation

Time Frame: up to 6 months

Number of participants who complete PrEP consultation and start PrEP

Retention

Time Frame: up to 6 months

Number of participants who come back for 3 month and 6 month visit

Follow Through

Time Frame: up to 6 months

Number of participants who pick up PrEP medication

Negative HIV Status at 6 months

Time Frame: up to 6 months

Number of participants who remain HIV negative at 6 months (Measured via negative HIV test at 6 months)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Duke University
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials