Drug Injection Surveillance and Care Enhancement for Rural Northern New England (UH3)

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Current or past history of drug injection;

• Health insurance that will cover HCV medications (study staff will work with those who are eligible but have not signed up for insurance prior to study enrollment)

• Lives in one of the study counties in NH and VT, and plans to remain in the study region for the next 12 months;

• Age 18 years or older;

• Speaks English;

• Capacity to voluntarily provide informed consent;

• Will accept randomized assignment, and participate in follow-up over 12 months;

• Will provide releases to access community medical records;

• Will provide names and contact information of at least 3 persons for re-contact purposes;

⁃ Not previously treated for HCV;

⁃ Not pregnant or trying to conceive;

⁃ HCV antibody positive on point-of-care rapid test.

Locations
United States
New Hampshire
Mobile Study Van
RECRUITING
Keene
Vermont
Mobile Study Van
RECRUITING
Bennington
Mobile Study Van
RECRUITING
Brattleboro
Contact Information
Primary
Randall A Hoskinson
randall.hoskinson@baystatehealth.org
413-794-7034
Backup
Lizbeth Del Toro-Mejias
lizbeth.deltoro-mejias@baystatehealth.org
787-462-1262
Time Frame
Start Date: 2022-05-18
Estimated Completion Date: 2024-07-31
Participants
Target number of participants: 220
Treatments
Experimental: Mobile Tele-HCV Care
Direct Acting Antiviral (DAA) treatment for HCV on a mobile van via telemedicine
Active_comparator: Enhanced Usual Care
Referral with care navigation to a local or regional HCV treatment provider
Related Therapeutic Areas
Sponsors
Collaborators: National Institute on Drug Abuse (NIDA), Tufts University, Dartmouth-Hitchcock Medical Center, University of Vermont, Better Life Partners Inc, University of New Hampshire
Leads: Baystate Medical Center

This content was sourced from clinicaltrials.gov