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Implementing HCV Treatment for High-risk Populations in Austin, Texas

Primary Purpose

Hepatitis C Virus Infection

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Simplified Hepatitis C Virus (HCV) Treatment Protocol
Sponsored by
University of Texas at Austin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatitis C Virus Infection focused on measuring DAAs, SVR12, Implementation Science, homelessness, direct-acting antivirals, sustained virological response, healthcare for the homeless, people who inject drugs

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patients age 18 years and older.
  • Enrolled in care at one of CommunityCare's clinical sites participating in the study.
  • Laboratory diagnosis of HCV
  • Chronic hepatitis C infection

Exclusion Criteria:

  • Have decompensated cirrhosis.
  • Have received hepatitis C treatment previously.
  • Had a liver transplant or actively on the transplant list awaiting a liver transplant.
  • Have resistant HCV virus
  • Infected with HIV
  • Infected with hepatitis B
  • Currently pregnant

Sites / Locations

  • CommUnityCare Health Centers

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Study Participants

Arm Description

Persons infected with the hepatitis C virus who meet the study inclusion criteria and do not meet one or more of the exclusion criteria.

Outcomes

Primary Outcome Measures

Proportion of participants with chronic HCV infection enrolled in the study that achieve SVR-12
A sustained virological response is defined as an undetectable HCV RNA level 12 weeks after treatment completion.

Secondary Outcome Measures

Clinical outcome: Time to treatment
Time elapsed (in days) from being offered treatment to initiating treatment
Clinical outcome: Complete HCV Treatment
Proportion of participants enrolled in the study who complete HCV treatment
Clinical outcome: Initiate HCV treatment
Proportion of participants enrolled in the study who initiate HCV treatment

Full Information

First Posted
July 7, 2022
Last Updated
April 4, 2023
Sponsor
University of Texas at Austin
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1. Study Identification

Unique Protocol Identification Number
NCT05460130
Brief Title
Implementing HCV Treatment for High-risk Populations in Austin, Texas
Official Title
Implementation of a Simplified, Low-barrier Primary Care HCV Treatment Model for High Risk, High Prevalence Populations in Austin, Texas
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
September 29, 2022 (Actual)
Primary Completion Date
June 2023 (Anticipated)
Study Completion Date
September 20, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas at Austin

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Highly-effective, pan-genotypic direct acting antivirals (DAAs) have made elimination of hepatitis C virus (HCV) a real possibility. A minority of the population infected with HCV has access to care or been prescribed such HCV treatment. Among people experiencing homelessness in the US, and seeking care at Health Care for the Homeless (HCH) clinics, prevalence is 31%, and 70% among people who experience homeless and inject drugs. In N. America, 55% of people who inject drugs (PWID) have HCV. Austin, TX has over 7,000 people experiencing homelessness with about 20% having a substance use disorder. Treatment of HCV via DAAs is feasible and effective in primary care settings, and is as effective as treatment by specialists. Among people with opioid use disorder receiving opioid agonist therapy it's both effective and cost-effective. Treatment in the primary care setting has also been shown to be feasible and effective for people experiencing homelessness, with supporting evidence of engaging and retaining people in care. Furthermore, a novel HCV treatment model, featuring a simplified HCV treatment algorithm for front-line health care providers (primary care physicians, Nurse Practitioners, Physicians Assistants), has now been published, to help increase capacity, scale-up treatment and achieve elimination. This study takes the foregoing new simplified approach one step further: Implementing this simplified algorithm for front-line health care providers in primary care settings caring for high-risk populations such as individuals experiencing homelessness and PWID. The novelty is providing treatment in diverse primary care settings, and targeting clinical sites serving high-risk populations, including people experiencing homelessness and PWID. Investigators use an implementation science approach to study the feasibility and effectiveness of the HCV treatment model in achieving HCV cure in high-risk populations. Investigators hypothesize that by training front-line health care providers on a simplified, low-barrier HCV treatment model and adapting it using a locally contextualized, protocol-driven approach, investigators will effectively scale up HCV treatment across multiple primary care clinical sites serving high-risk populations, yielding sustained virologic response at 12 weeks (SVR-12) in 75% of enrolled participants. Investigators predict theHCV treatment model to measure favorably across implementation process and outcome measures of reach, adoption, implementation, and maintenance.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C Virus Infection
Keywords
DAAs, SVR12, Implementation Science, homelessness, direct-acting antivirals, sustained virological response, healthcare for the homeless, people who inject drugs

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study Participants
Arm Type
Other
Arm Description
Persons infected with the hepatitis C virus who meet the study inclusion criteria and do not meet one or more of the exclusion criteria.
Intervention Type
Behavioral
Intervention Name(s)
Simplified Hepatitis C Virus (HCV) Treatment Protocol
Intervention Description
A simplified, low-barrier, locally contextualized, HCV treatment protocol delivered by trained front-line health care providers (primary care physicians and mid-level providers) serving hard-to-reach-populations.
Primary Outcome Measure Information:
Title
Proportion of participants with chronic HCV infection enrolled in the study that achieve SVR-12
Description
A sustained virological response is defined as an undetectable HCV RNA level 12 weeks after treatment completion.
Time Frame
The measurement of SVR12 is assessed 12 weeks after completing treatment.
Secondary Outcome Measure Information:
Title
Clinical outcome: Time to treatment
Description
Time elapsed (in days) from being offered treatment to initiating treatment
Time Frame
Approximately 10 months from time of enrollment
Title
Clinical outcome: Complete HCV Treatment
Description
Proportion of participants enrolled in the study who complete HCV treatment
Time Frame
Approximately 10 months from time of enrollment
Title
Clinical outcome: Initiate HCV treatment
Description
Proportion of participants enrolled in the study who initiate HCV treatment
Time Frame
Approximately 10 months from time of enrollment
Other Pre-specified Outcome Measures:
Title
Implementation Outcome: Reach
Description
Proportion of participants with chronic HCV enrolled in the study who are offered treatment
Time Frame
Approximately one year from date of enrollment of first participant
Title
Implementation Outcome: Adoption
Description
Proportion of clinical sites that adopt the HCV treatment protocol
Time Frame
Approximately one year from date of enrollment of first participant
Title
Implementation Outcome: Implementation
Description
Qualitative interviews to assess the extent to which the HCV treatment protocol was implemented as intended (fidelity)
Time Frame
Approximately one year from date of enrollment of first participant
Title
Implementation Outcome: Maintenance
Description
Qualitative interviews to assess the extent to which the HCV treatment protocol is sustained over time
Time Frame
Approximately one year from date of enrollment of first participant

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients age 18 years and older. Enrolled in care at one of CommunityCare's clinical sites participating in the study. Laboratory diagnosis of HCV Chronic hepatitis C infection Exclusion Criteria: Have decompensated cirrhosis. Have received hepatitis C treatment previously. Had a liver transplant or actively on the transplant list awaiting a liver transplant. Have resistant HCV virus Infected with HIV Infected with hepatitis B Currently pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Timothy I Mercer, MD,MPH
Organizational Affiliation
The University of Texas at Austin Dell Medical School
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Darlene Bhavnani, PhD MPH
Organizational Affiliation
The University of Texas at Austin Dell Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
CommUnityCare Health Centers
City
Austin
State/Province
Texas
ZIP/Postal Code
78704
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Implementing HCV Treatment for High-risk Populations in Austin, Texas

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