Rural New England Health Study (Phase 2)

NCT05466331 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 220

Last updated 2023-12-01

No results posted yet for this study

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

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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05466331 on ClinicalTrials.gov