Identification to Elimination in HCV-Infected Individuals

Early Phase 1

Completed

• Conditions: Hepatitis C
• Interventions: Diagnostic Test: OraQuick HCV Rapid Antibody Test

• Registration Number: NCT03195205
• Lead Sponsor: TruCare Internal Medicine & Infectious Disease

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.

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 Timeline

• Study First Submitted: 2017-05-31
• Study Start: 2017-06-01
• Study First Submitted QC: 2017-06-19
• Study First Posted: 2017-06-22
• Primary Completion: 2020-04-20
• Study Completion: 2020-04-20
• Status Verified: 2020-07
• Last Update Submitted: 2020-07-01
• Last Update Posted: 2020-07-02

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 3051

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
High-Risk Patients	OraQuick HCV Rapid Antibody Test	OraQuick HCV screening for HCV-Infected Individuals on Opioid Substitution Therapy and High-Risk Populations

Primary Outcome Measures

Name	Time	Method
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

Name	Time	Method
Treatment	8 - 24 weeks	The study will measure the percentage of patients linked to care who complete treatment.
Linked to care	1 - 3 months	The study will measure the percentage of patients identified as reactive that follow up by linking to care.

Trial Locations

Locations (1)

TruCare Internal Medicine & Infectious Diseases; 🇺🇸 DuBois, Pennsylvania, United States