Rural New England Health Study (Phase 2)
NCT05466331 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 220
Last updated 2023-12-01
Summary
This study will integrate mobile hepatitis C virus (HCV) testing and treatment with expanded syringe access in order to improve uptake of HCV testing and treatment, and reduce syringe sharing behavior in rural northern New England. The intervention aims to reach rural opioid injectors with HCV and to fill service gaps identified around access to syringe services and HCV testing and treatment, while limiting the burden on local partners. If effective, this mobile model of HCV telehealth integrated with syringe services will provide a promising approach for local public health authorities seeking to curb opioid injection, syringe sharing and HCV rates in rural America, and reduce the risk environment for HIV outbreaks in those communities.
Conditions
- Hepatitis C
- Opioid Use Disorder
- IV Drug Usage
Interventions
- OTHER
-
Mobile Tele-HCV Care
Study participants receive HCV care via telemedicine. Telemedicine appointments are performed on a mobile van.
- OTHER
-
Enhanced Usual Care
Study participants are referred to a clinician in their area for HCV care.
Sponsors & Collaborators
-
Tufts University
collaborator OTHER -
University of New Hampshire
collaborator OTHER -
University of Vermont
collaborator OTHER -
Dartmouth-Hitchcock Medical Center
collaborator OTHER -
Better Life Partners Inc
collaborator UNKNOWN -
National Institute on Drug Abuse (NIDA)
collaborator NIH -
Baystate Medical Center
lead OTHER
Principal Investigators
-
Peter D Friedmann, MD, MPH · Baystate Medical Center
-
Thomas J Stopka, PhD, MHS · Tufts University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2022-05-18
- Primary Completion
- 2024-07-31
- Completion
- 2024-07-31
Countries
- United States
Study Locations
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