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Accessible HCV Care Intervention for People Who Inject Illicit Drugs (PWID)

Not Applicable
Completed
Conditions
PWID
People Who Inject Drugs
Hepatitis C
HCV Coinfection
Interventions
Other: Usual Care
Other: Accessible Care
Registration Number
NCT03214679
Lead Sponsor
City University of New York, School of Public Health
Brief Summary

The proposed study will examine the feasibility, acceptability, safety, effectiveness, and cost of an Accessible Care intervention for engaging people who inject illicit drugs (PWID) in hepatitis C care. Accessible Care for PWID is low-threshold care provided in programs designed specifically for PWID where they can comfortably access care without fear of shame or stigma. Accessible Care will be provided by co-locating a hepatitis treatment provider, together with a Hepatitis C Care Coordinator (HCCC), on-site at a collaborating needle exchange program. The proposed study will compare the effectiveness of Accessible Care with Usual Care (referrals to existing services) in facilitating linkage, engagement, and retention of PWID in care for hepatitis C, addiction, and HIV prevention. The primary outcome is sustained virologic response, which constitutes virologic cure. Substance use and HIV and HCV risk behaviors are secondary outcomes.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
167
Inclusion Criteria
  1. 18 years or older,
  2. injected heroin, cocaine, or other drugs in the past 90 days.
  3. test HCV Ab and RNA positive
  4. provide written consent (including consent for researchers to examine their hepatitis C medical records)
Exclusion Criteria

Persons already in care for hepatitis C, defined as having had at least 2 visits with a hepatitis treatment provider within the past 6 months, will be excluded.

People with decompensated cirrhosis will be excluded.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Usual CareUsual CareUsual care represents the current process after someone tests positive for HCV antibody on site at the syringe exchange program. An on site care coordinator (not provided by study) assists with insurance and linkage to HCV medical provider at sites throughout NYC through the NYC Dept of Health Check Hep C program.
Accessible CareAccessible Care"Accessible Care" for PWID is low-threshold care provided in the needle exchange programs, where they can comfortably access services without fear of the shame or stigma that often attends them in mainstream institutions.It includes features such as an informal, nonjudgmental atmosphere, availability of walk-in appointments, and a harm reduction framework to help them identify and pursue their own personal health goals. Accessible Care will be provided by co-locating a hepatitis treatment provider, together with a Hepatitis C Care Coordinator, on-site at our collaborating needle exchange program.
Primary Outcome Measures
NameTimeMethod
Proportion of Patients in Each Arm Referred to Hepatitis C Treatment Providereach participant will be assessed at 1 year post entry

Proportion of patients in each arm referred to hepatitis C treatment provider by 12 months

Proportion of Patients to Achieve SVR12 at 1 Yeareach participant will be assessed at 1 year post entry

SVR12 is a sustained virologic response to HCV treatment defined as HCV RNA below the limit of quantification 12 weeks post completion of HCV treatment

Proportion of Participants in Each Arm Who Initiated TreatmentEach participant will be assessed 1 year post entry

Proportion of participants in each arm physically receiving the first dose of antiviral medication (without necessarily having confirmed ingestion)

The Proportion of Participants With Hepatitis C Treatment Engagement by 12 Months That Attended an Initial Visitend of study (12 months)

The proportion of participants in each arm who attend an initial visit with a hepatitis treatment provider post randomization.

Proportion of Patients in Each Arm Who Complete a Medical Evaluation for Antiviral Treatmenteach participant will be assessed at 1 year post entry

Proportion of patients in each arm who complete a medical evaluation for antiviral treatment, including a history, physical examination and laboratory evaluation

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Lower East Side Harm Reduction Center

🇺🇸

New York, New York, United States

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