Partner Navigation for Hepatitis C and Substance Use Disorder
What You Need to Know Before You Apply
What is the purpose of this trial?
This study builds upon an ongoing NIH-funded randomized controlled trial (R01DA053325) evaluating a Partner Navigation Intervention to increase hepatitis C virus (HCV) treatment initiation among young adult people who inject drugs (PWID) and their injecting partners in San Francisco. The proposed research includes secondary analyses of existing trial data, additional survey measures, qualitative interviews, and a pilot intervention adaptation.
The study has two primary objectives. First, it examines how racialized discrimination (structural, interpersonal, and internalized) affects HCV treatment initiation and dyadic partner support processes within injecting partnerships. Second, it evaluates whether a brief, adapted "booster" partner navigation session delivered at HCV treatment completion can improve engagement in ongoing healthcare.
Participants include adults (≥18 years) who inject drugs and have been diagnosed with HCV, along with their primary injecting partners. Study activities include longitudinal surveys, qualitative interviews with a subset of participants, and a pilot intervention session with follow-up evaluation.
This research addresses critical gaps in understanding how social relationships and structural inequities influence healthcare engagement among PWID. Findings will inform culturally responsive adaptations to dyadic interventions and improve continuity of care in a population disproportionately affected by HCV and systemic barriers to healthcare.
Who Is on the Research Team?
Meghan Morris, PhD, MPH
Principal Investigator
University of California, San Francisco
Are You a Good Fit for This Trial?
This trial is for adults (18+) who inject drugs, have finished hepatitis C treatment in the last 3 months, and have a main injecting partner willing to join. Participants must speak English or Spanish and be able to give informed consent.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive HCV treatment and a Partner Navigation Intervention booster session at treatment completion
Follow-up
Participants are monitored for engagement in ongoing healthcare and session acceptability
What Are the Treatments Tested in This Trial?
Interventions
- Partner Navigation Intervention Booster Session
Trial Overview
The study tests if a brief 'booster' session with both partners after finishing hepatitis C treatment helps people stay engaged in healthcare. It uses surveys, interviews, and follow-up checks to see how well this approach works.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Injecting dyads (index participant and their primary injecting partner) receive one adapted Partner Navigation Intervention booster session at the point of HCV treatment completion, designed to strengthen partnership-based support for sustained healthcare engagement beyond HCV care.
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of California, San Francisco
Lead Sponsor
National Institute on Drug Abuse (NIDA)
Collaborator
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