Identification to Elimination in HCV-Infected Individuals

Sponsor
TruCare Internal Medicine & Infectious Disease (Other)
Overall Status
Completed
CT.gov ID
NCT03195205
Collaborator
Gilead Sciences (Industry)
3,051
1
1
34.6
88.1

Study Details

Study Description

Brief Summary

Approximately 3.5 - 5 million Americans are living with hepatitis C virus (HCV) in the United States. HCV significantly impacts rural Pennsylvania. It is estimated that 160,000 adults in Pennsylvania are living with hepatitis C. In 2010, Center for Rural Pennsylvania estimated that 27% of population of PA live in one of Pennsylvania's 48 rural counties. Under this estimate, there are over 43,000 individuals affected with chronic HCV living in rural Pennsylvania. Rural county residents often experience barriers to health care by having fewer primary care providers and limited specialty care physicians available to them to address their healthcare needs.

RQ1: Will the community based delivery system for Hepatitis C screenings see an increase in positivity rates?

HO1: There is no relationship between the community based delivery system with an increase in the Hepatitis C screening positivity rates.

HA1: There is a relationship between the community based delivery system with an increase in the Hepatitis C screening positivity rates.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: OraQuick HCV Rapid Antibody Test
Early Phase 1

Detailed Description

In rural Pennsylvania, transportation is considered a socioeconomic barrier and social detriment to personal health. Using an evidence-based model of population health by bringing the care into the high-risk population's community setting reduces the transportation and socioeconomic barriers of the most vulnerable at risk populations.

It is estimated that 35% to 65% of Opioid Substitution Treatment Patients (OST), are infected with HCV. Therefore, OPT programs that are already operating will be engaged and will be a primary focus for patient screening and recruitment for these services. In addition, high volume venues attracting high-risk populations will also be targeted to encourage HCV screening, education, and treatment.

Primary Objectives:

To screen Opioid Substitution Treatment Patients (OST), high-risk individual at Opioid Treatment Programs (OTP), and/or all high-risk populations in outlying sites (Anti-HCV prevalence)

To initiate HCV treatment of OST patients and other high-risk individuals at OTP facilities and/or high risk populations in outlying sites (linkage of care)

To maintain the successful HCV therapy and cure [Sustained Viral Response (SVR)] in OST patients and other high-risk individuals at OPT facility and/or high risk populations in outlying sites (retention)

To facilitate the use of a patient navigator and nursing case management staff to reduce barriers to initial screening and patient education

Study Design

Study Type:
Interventional
Actual Enrollment :
3051 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
A Novel Approach Continuum to Identification to Elimination in HCV-Infected Individuals on Opioid Substitution Therapy and High-Risk Populations
Actual Study Start Date :
Jun 1, 2017
Actual Primary Completion Date :
Apr 20, 2020
Actual Study Completion Date :
Apr 20, 2020

Arms and Interventions

Arm Intervention/Treatment
Other: High-Risk Patients

OraQuick HCV screening for HCV-Infected Individuals on Opioid Substitution Therapy and High-Risk Populations

Diagnostic Test: OraQuick HCV Rapid Antibody Test
HCV Screening

Outcome Measures

Primary Outcome Measures

  1. Positivity rates [20 - 40 minutes]

    The study will measure the percentage of patients screened for Hepatitis C who are reactive by detecting HCV antibodies.

Secondary Outcome Measures

  1. Linked to care [1 - 3 months]

    The study will measure the percentage of patients identified as reactive that follow up by linking to care.

  2. Treatment [8 - 24 weeks]

    The study will measure the percentage of patients linked to care who complete treatment.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
Subjects will be included in the study if the following criteria is met:
  1. The subject must be an Opioid Substitution Treatment patient.

  2. The subject must fall into another high-risk population for the HCV.

Exclusion Criteria:

Subjects may be excluded from the study if the subject falls into an exclusion category as identified as:

  1. The subject cannot be or suspected of being pregnant

  2. The subject cannot be under the age of 18 years.

  3. No subjects requiring a legally authorized representative will be enrolled

Contacts and Locations

Locations

Site City State Country Postal Code
1 TruCare Internal Medicine & Infectious Diseases DuBois Pennsylvania United States 15801

Sponsors and Collaborators

  • TruCare Internal Medicine & Infectious Disease
  • Gilead Sciences

Investigators

  • Principal Investigator: Tuesdae R Stainbrook, DO, MPH, Trucare Internals Medicine & Infectious Disease

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tuesdae Stainbrook, DO, MPH, Principal Investigator, TruCare Internal Medicine & Infectious Disease
ClinicalTrials.gov Identifier:
NCT03195205
Other Study ID Numbers:
  • GSI-2016-09-APR
First Posted:
Jun 22, 2017
Last Update Posted:
Jul 2, 2020
Last Verified:
Jul 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 2, 2020