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Eliminate Hepatitis C/EC Partnership Evaluation Protocol

Primary Purpose

Hepatitis C, Chronic Hepatitis c, Hepatitis C, Chronic

Status
Unknown status
Phase
Not Applicable
Locations
Australia
Study Type
Interventional
Intervention
EC clinic support - whole of practice interventions delivery through nurse-led model
Sponsored by
Macfarlane Burnet Institute for Medical Research and Public Health Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Hepatitis C

Eligibility Criteria

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

The level of recruitment is clinics rather than individuals. Eligible clinics are those with a high HCV caseload, with a focus on drug and alcohol community clinics and general practitioners.

Eligibility criteria for individuals providing information in the form of interviews will be:

  • 18 years of age or older; AND
  • Willing and able to provide informed, written consent to participate; AND
  • Either of:

    • staff of a participating EC site who are involved in hepatitis C care; OR
    • clients of a participating EC site who attend the site for screening and management of hepatitis C.

Sites / Locations

  • Burnet InstituteRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

EC Clinic Support

Arm Description

Whole of practice interventions delivery through nurse-led model

Outcomes

Primary Outcome Measures

Uptake of treatment amongst PWID
The number of PWID who commence HCV treatment across EC partnerships sites over time and compared to tertiary care models

Secondary Outcome Measures

Treatment effectiveness relative to tertiary care services
Rates of cure, assessed as sustained virological response at 12 weeks post treatment completion (SVR12), and treatment failure amongst PWID treatment in community and prison-based services will be compared to tertiary-based treatment programs.
Costs of scaling up treatment for PWID
The costs of treating >1,160 PWID within the community and prison services will be assessed.
Changes in HCV prevalence and incidence in Victoria
HCV prevalence and incidence will be tracked during the project and compared to historical data.
Projected impact on HCV elimination targets
Mathematical modelling studies will assess the expected impact the changes in treatment uptake, incidence and prevalence will have on the WHO incidence and mortality targets for viral hepatitis elimination. This will be used to provide an estimate of the feasibility of achieving elimination targets in Australia and in other countries.

Full Information

First Posted
June 4, 2019
Last Updated
August 22, 2021
Sponsor
Macfarlane Burnet Institute for Medical Research and Public Health Ltd
Collaborators
Burnet Institute, The Alfred, St Vincent's Hospital Melbourne, HepatitisVictoria, Harm Reduction Australia, Victoria State Government, Gilead Sciences, National Health and Medical Research Council, Australia
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1. Study Identification

Unique Protocol Identification Number
NCT04061551
Brief Title
Eliminate Hepatitis C/EC Partnership Evaluation Protocol
Official Title
Eliminate Hepatitis C/EC Partnership Evaluation Protocol
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
December 2016 (Actual)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Macfarlane Burnet Institute for Medical Research and Public Health Ltd
Collaborators
Burnet Institute, The Alfred, St Vincent's Hospital Melbourne, HepatitisVictoria, Harm Reduction Australia, Victoria State Government, Gilead Sciences, National Health and Medical Research Council, Australia

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
The Eliminate Hepatitis C (EC) Partnership project is a multi-site, multi-year project aiming to enhance and extend hepatitis C virus (HCV) care and treatment among people who inject drugs (PWID) through nurse-led models of care in the community and the prison system. The project will implement and evaluate a health service intervention to enhance HCV response by improving health promotion, offering training and education to service providers, streamlining clinical pathways, utilising data systems and surveillance and implementing the results of ongoing research and evaluation. Health services data will be used to assess the impact of the EC nurse-led support, to enhance the clinical pathway and increase HCV testing, linkage to care and treatment uptake in community and prison settings. This will include provider and client interviews and a sentinel surveillance system (ACCESS) that will track and monitor impact indicators including HCV testing, linkage to care and treatment uptake at the service and population level. Overall, evaluation data will be used to monitor the uptake of HCV treatment in PWID, monitor the effectiveness of community- and prison-based treatment program and assess the cost and feasibility of treating >1160 PWID in community-/prison-based program and assess changes in HCV prevalence in Victoria and modelling the impact of treating PWID to inform HCV elimination models in Australia and globally.
Detailed Description
An estimated 71 million people are living with hepatitis C virus (HCV) world-wide, at significant risk of morbidity and mortality from liver cirrhosis, liver failure and hepatocellular carcinoma. However, the development of well-tolerated, highly-efficacious curative direct-acting antiviral treatment (DAAs) has contributed to a global push to eliminate HCV as a public health threat. The World Health Organization has developed a global strategy for elimination that calls for 90% of people living with HCV to be diagnosed and 90% of those diagnosed to be treated by 2030. In 2015, prior to the DAAs being released, it was estimated that around 230,000 people living with HCV in Australia. Like in many other high-income countries, the group most affected by HCV in Australia are people who inject drugs (PWID), making this a key population group for Australia's HCV elimination efforts. Despite the availability of DAAs through Australia's Pharmaceutical Benefits Scheme (PBS), numerous barriers exist for PWID to access HCV care and particularly to accessing tertiary-based care. As such, targeting community-based services that provide comprehensive care packages for PWID, including the provision of opioid substitution therapy (OST), counselling, a needle and syringe program (NSP) for the delivery of HCV treatment should increase PWIDs' engagement in HCV care. The EC Partnership program has been funded to increase capacity of community and prison services to provide HCV testing and treatment with DAA treatments by streamlining clinical pathways and reducing barriers to access. The EC Partnership project is a multi-site, multi-year project aiming to enhance and extend hepatitis C virus (HCV) care and treatment among people who inject drugs (PWID) through nurse-led models of care in the community and the prison system. Specifically the project aims to: Increase demand for HCV treatment among PWID; Increase the capacity of community services to provide HCV testing & treatment with PBS listed DAAs; Increase the capacity to provide HCV testing & treatment in prison with PBS listed DAAs; Streamline clinical pathways (tailored for different types of settings) to increase access to PBS listed DAAs; and Establish an integrated HCV surveillance system to more accurately monitor trends in HCV prevalence and incidence over time. To achieve this, the project will implement and evaluate a health service intervention for prison-based and community-based health services providing care to PWID. The intervention will have five main components: enhance HCV response by improving health promotion; offering training and education to service providers; streamlining clinical pathways; utilising data systems and surveillance; and implementing the results of ongoing research and evaluation. The intervention will be evaluated using qualitative and quantitative data from health services, clinical providers and clients, which will include: EC experience observational cohort data will assess predictors of patient engagement and identify barriers and enablers to progression through the cascade of care Interviews with clinical service providers to assess changes to clinical pathways and to inform cost-effectiveness analysis Clinical data from the Australian Collaboration for Co-ordinated Sentinel Surveillance (ACCESS) System that will track and monitor impact indictors including HCV testing, linkage to care and treatment uptake at the service and population level Data from State-wide Hepatitis Assessment and Management Program (Prison programs) Data from Medicare, PBS and other Victorian Department of Health and Human Services datasets (This will occur with a subset of patients who provide consent from participating sites). In addition, the project will incorporate a sub study (Ophelia evaluation) that will be used to guide development and implementation of health promotion initiatives. The EC Partnership evaluation aims to measure the overall impact of the EC Partnership by monitoring and evaluating specific key outcomes, including: Number of PWID who uptake HCV treatment across EC partnerships services within the community and the prison system; Treatment effectiveness (SVR12 cure rates & treatment failures) among community and the prison based treatment programs, compared to tertiary-based treatment programs; Cost and feasibility of treating >1,160 PWID within the community and the prison systems; Changes in HCV prevalence and incidence in Victoria, and comparing community and prison population estimates; Model the impact of treating PWID to inform HCV elimination models in Australia and globally.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C, Chronic Hepatitis c, Hepatitis C, Chronic

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
The comprehensive intervention will be implemented at all participating sites, although specific components of the intervention will be tailored to the needs of each site. The model consists of five stages: Baseline site assessment Co-design intervention to streamline HCV clinical pathways Implementation Six-monthly review End line review
Masking
None (Open Label)
Allocation
N/A
Enrollment
25 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
EC Clinic Support
Arm Type
Experimental
Arm Description
Whole of practice interventions delivery through nurse-led model
Intervention Type
Other
Intervention Name(s)
EC clinic support - whole of practice interventions delivery through nurse-led model
Intervention Description
The primary interventions will be delivered through a team of nurses, an evaluation team and practice support team that will be working with each of the services to improved Hepatitis C service delivery. The EC project team will predominantly be involved in working with providers and staff at EC sites to implement key interventions that have been collated into a Primary Care Practice Toolkit, which cover three domains; patient support, provider support and practice Support. The toolkit is designed to be an educational and implementation resource that the nursing team will support services to deliver. Patient support to reduce the impact of hepatitis C and other blood borne viruses Provider support to reduce the impact of hepatitis C and other blood borne viruses Practice support to reduce the impact of hepatitis C and other blood borne viruses
Primary Outcome Measure Information:
Title
Uptake of treatment amongst PWID
Description
The number of PWID who commence HCV treatment across EC partnerships sites over time and compared to tertiary care models
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Treatment effectiveness relative to tertiary care services
Description
Rates of cure, assessed as sustained virological response at 12 weeks post treatment completion (SVR12), and treatment failure amongst PWID treatment in community and prison-based services will be compared to tertiary-based treatment programs.
Time Frame
5 years
Title
Costs of scaling up treatment for PWID
Description
The costs of treating >1,160 PWID within the community and prison services will be assessed.
Time Frame
5 years
Title
Changes in HCV prevalence and incidence in Victoria
Description
HCV prevalence and incidence will be tracked during the project and compared to historical data.
Time Frame
5 years
Title
Projected impact on HCV elimination targets
Description
Mathematical modelling studies will assess the expected impact the changes in treatment uptake, incidence and prevalence will have on the WHO incidence and mortality targets for viral hepatitis elimination. This will be used to provide an estimate of the feasibility of achieving elimination targets in Australia and in other countries.
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
The level of recruitment is clinics rather than individuals. Eligible clinics are those with a high HCV caseload, with a focus on drug and alcohol community clinics and general practitioners. Eligibility criteria for individuals providing information in the form of interviews will be: 18 years of age or older; AND Willing and able to provide informed, written consent to participate; AND Either of: staff of a participating EC site who are involved in hepatitis C care; OR clients of a participating EC site who attend the site for screening and management of hepatitis C.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alisa Pedrana, PhD
Phone
+61392822225
Email
alisa.pedrana@burnet.edu.au
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Margaret E Hellard, MD PhD
Organizational Affiliation
Burnet Institute and Alfred Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Burnet Institute
City
Melbourne
State/Province
Victoria
ZIP/Postal Code
3004
Country
Australia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alisa Pedrana
Phone
61 3 9282 2225
Email
alisa.pedrana@burnet.edu.au

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27196586
Citation
Scott N, McBryde ES, Thompson A, Doyle JS, Hellard ME. Treatment scale-up to achieve global HCV incidence and mortality elimination targets: a cost-effectiveness model. Gut. 2017 Aug;66(8):1507-1515. doi: 10.1136/gutjnl-2016-311504. Epub 2016 Apr 12.
Results Reference
background
PubMed Identifier
28797497
Citation
Scott N, Doyle JS, Wilson DP, Wade A, Howell J, Pedrana A, Thompson A, Hellard ME. Reaching hepatitis C virus elimination targets requires health system interventions to enhance the care cascade. Int J Drug Policy. 2017 Sep;47:107-116. doi: 10.1016/j.drugpo.2017.07.006. Epub 2017 Aug 7.
Results Reference
background
PubMed Identifier
30908706
Citation
Doyle JS, Scott N, Sacks-Davis R, Pedrana AE, Thompson AJ, Hellard ME; Eliminate Hepatitis C Partnership. Treatment access is only the first step to hepatitis C elimination: experience of universal anti-viral treatment access in Australia. Aliment Pharmacol Ther. 2019 May;49(9):1223-1229. doi: 10.1111/apt.15210. Epub 2019 Mar 25.
Results Reference
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Eliminate Hepatitis C/EC Partnership Evaluation Protocol

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