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Advanced Care Coordination and Enhanced Linkage and Retention Among Transitional Re-Entrants

Not Applicable
Recruiting
Conditions
Hepatitis C
Interventions
Behavioral: Standard of care
Behavioral: Peer mentor
Registration Number
NCT04701437
Lead Sponsor
Montefiore Medical Center
Brief Summary

The overarching goal of this study is to develop a peer-based care coordination intervention for individuals with Hepatitis C Virus (HCV) who were recently released from correctional settings to promote linkage to and retention in HCV care. The investigators will assess the existing barriers and facilitators of HCV treatment initiation, HCV treatment completion, and sustained virologic response among individuals recently released from a U.S. jail or prisons in a randomized control trial. This study will assess the feasibility and process measures of a peer-enhanced HCV care coordination intervention among recently incarcerated individuals.

Detailed Description

The proposed 2-year study will be a block stratified, randomized controlled trial. Once consented and enrolled, participants will be randomly assigned to either the peer-enhanced intervention or referred to standard clinical care. The investigators will enroll 80 former inmates with chronic HCV who have been released from incarceration within the past 6 months. It is expected that enrollment will be completed by the fourth quarter of the first year. This will allow sufficient time for HCV treatment uptake, completion, determination of Sustained Virologic Response (SVR), and assessment of reinfection. Individual participant follow-up will be 3 months on average for treatment, 3 months for SVR, and 3 months to assess for reinfection.

Elucidating the barriers and facilitators in the re-entry care cascade (as well as how they may be overcome) will be critical in designing sustainable models of care for HCV-infected former inmates. The investigators hypothesize that a peer-enhanced strategy will be more effective than standard referral in improving linkage to, and retention in, HCV care among individuals recently released from correctional settings.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
80
Inclusion Criteria
  • currently incarcerated or recently released from a U.S. jail or prison (6 months)
  • Chronic HCV with documented detectable viral load
  • 18 years old
  • Fluent in English or Spanish
  • Resident of the Upstate area of South Carolina
Exclusion Criteria
  • Unable to sign informed consent
  • Life expectancy of less than 1 year
  • Plans to relocate from the Upstate area of South Carolina in the next 6 months

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Standard of careStandard of careIf randomized to the standard of care intervention, the participant will only receive passive referral to HCV-care.
Peer-enhanced interventionPeer mentorThose randomized to the peer-enhanced intervention group will be contacted by a peer mentor within 72 hours of enrollment to discuss the early release period, readiness for HCV treatment, and identify ancillary needs. Individuals randomized to this arm will be provided a study cell phone.
Primary Outcome Measures
NameTimeMethod
Linkage to care6 months

A visit with an HCV treatment provider

Secondary Outcome Measures
NameTimeMethod
HCV cure3 months after treatment completion

Achieving HCV cure, as determined by EMR

Treatment completionup to 3 months after treatment initiation

Completing HCV treatment, as determined by EMR

Reinfection12 months after treatment completion

Determined by EMR

HCV treatment initiationup to 3 months after linkage to care

Initiating HCV treatment and the number of days following release from the correctional setting to initiation of HCV treatment

Trial Locations

Locations (1)

Prisma Health-Upstate

🇺🇸

Greenville, South Carolina, United States

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