Hepatitis C Clinical Trial
Official title:
HepCare: The Effectiveness of Community Based Interventions With Peer Support to Improve Case Detection, Carry Out Pre-treatment Assessments and Assist Underserved Populations Through HCV Treatment
Hepatitis C infection is a major cause of chronic liver disease and death with approximately
3% of the world's population is infected with hepatitis C virus (HCV).
New drug therapies called new direct-acting antivirals (DAAs) have been developed and have
proven to be well tolerated with minimal side effects. The current costs of these agents are
extremely high, however, they provide an opportunity to cure most patients of HCV if they can
access and adhere to treatment. The bigger challenge is to engage and cure underserved groups
who are not accessing medical care, or who have other complex problems, including
homelessness, incarceration, and substance misuse problems.
Strategies to improve HCV case detection and case management have much to learn from other
infectious diseases. Tuberculosis (TB) disproportionately affects in large part the same
group of individuals and community models of care have been used with great success.
Strategies such as active case finding, community based screening and treatment, directly
observed therapy (DOT) and peer support have all shown high rates of case detection and
treatment completion.
These strategies are currently being used by the Find&Treat team, UCLH NHS Trust and this
study will ain in evaluating it's effectiveness. Previously used to aid homeless patients
engage with treatment services for TB, it is now being used with other disease groups such as
HCV.
This observational study aims to assess the effectiveness of community based interventions
with peer support to improve case detection, carry out pre-treatment assessments and assist
underserved populations through HCV treatment by the Find&Treat service.
1. Introduction
Hepatitis C infection is a major cause of chronic liver disease and death throughout the
world1. Approximately 3% of the world's population is infected with hepatitis C virus
(HCV)2.
HCV is transmitted by blood and in the UK occurs primarily through injecting drug use.
Chronically infected people are at risk of progressive liver disease characterised by
hepatocellular inflammation, hepatic fibrosis, cirrhosis and hepatocellular carcinoma
(HCC). These complications develop only in a proportion of patients and only after many
years or decades of infection3. It has been estimated that up to 20% of chronically
infected individuals will develop cirrhosis of the liver over a 20 to 25 year period.
Approximately 3% to 4% of patients with cirrhosis will develop HCC per year3.
New drug therapies such as protease and polymerase inhibitors called direct-acting
antivirals (DAAs) have been developed in the last ten years and have recently been
licensed for use worldwide. These DAAs have proven to be very well tolerated with
minimal, and sometimes no, side effects. The current costs of these agents are extremely
high, limiting their use to select populations of infected patients. However, they
provide an opportunity to cure most patients with HCV if they can access and adhere to
treatment. A bigger challenge is to engage and cure those who are not accessing medical
care, or who have other complex problems, including homelessness, incarceration, and
substance misuse. These underserved populations are disproportionately affected by
infectious diseases such as HCV and face many challenges to access testing and adherence
to treatment.
There has been previously demonstrated a high prevalence (13% RNA detectable HCV4) of
chronic HCV infection among homeless people opportunistically screened at residential
hostels and day centres across London. Data from the HALT Hepatitis Study5 showed that
41% of HCV Ab positive recruits were homeless at enrolment and that over 60% of HCV
infected patients knew of their status but had disengaged from treatment services. This
population therefore includes a high number of undiagnosed cases and previously known
HCV positive cases who are not accessing treatment services.
The epidemiology of HCV among homeless populations in the UK is poorly understood.
Currently there are no data on the extent of liver fibrosis in this population to inform
strategies for future management and estimate potential resource requirements to
effectively mobilise treatment to this vulnerable and underserved group. Early detection
of significant fibrosis is critical to prevent severe disease and death. Ongoing drug or
alcohol use is not a contra-indication to hepatitis C treatment, and research shows that
people who are actively using drugs can and should be treated for hepatitis C6. Point of
care tests (POCTs) mean that infection can be identified immediately in the community
reducing the risk of loss to follow up. Transient liver elastography (performed using
FibroScan®) is now the gold standard in the assessment for liver fibrosis. FibroScanning
is a 5 minute non-invasive, painless procedure to accurately assess liver fibrosis with
high reproducibility7. This means that mush of what traditionally required several
hospital appointments can now be done in potentially one outreach session.
Strategies to improve HCV case detection and management have much to learn from the
management of Tuberculosis (TB), a disease which affects the same group of individuals
and community models of care have been used with great success. Strategies such as
active case finding, community based screening and treatment, directly observed therapy
(DOT) and peer support have all shown high rates of case detection and treatment
completion.
The Find&Treat Mobile Health Unit (MHU) from UCLH NHS Trust provides health screening
for homeless individuals across various sites in London, UK such homeless hostels, day
centres and drug services. They are experienced in using outreach models of care and
peer advocates for infectious diseases such as TB to engage patients with specialist
care. As HCV treatment moves into the community there is a need to evaluate outreach
activities to inform future practice and care.
2. Aims and Objectives
This study aims to assess the effectiveness of community based interventions with peer
support to improve case detection, carry out pre-treatment assessments and assist
underserved populations through HCV treatment by the Find&Treat service.
Primary Objective
Evaluate the effectiveness of the HCV community based detection and management including
screening, liver assessment and treatment support in underserved populations using
mobile health facilities and peer support.
Secondary Objectives
- Estimate the proportion of homeless people with chronic HCV infection and their
degree of liver fibrosis.
- Risk factors for HCV infection and for re-infection for those completing treatment
or testing negative at recruitment.
- Report this experience to inform the development of further programmes in the UK
and other EU countries.
3. Study design
This is an observational study to establish the effectiveness of intensified community based
screening, liver assessment and supported treatment for homeless people and underserved
populations. Patients will be recruited from an NHS mobile health outreach service screening
individuals accessing homeless and drug services in London, UK.
Following enrolment patient will be followed up for up to 12 months or until an appropriate
defined clinical end point is reached. Successful engagement with community based HCV
screening and treatment is defined as:
i. Successful pre-treatment assessment and a decision to not proceed by the clinician ii.
Engagement with treatment support (including offered, start or completion of therapy
according to individual circumstance)
Preliminary data from the HALT study (1) shows an effect size in improved engagement of 1.9.
To detect a 20% increase in individuals successfully engaging with community services, from a
baseline of 20%, we would need to recruit 164 individuals who are HCV positive (with 90%
power and 5% significance level) compared with 82 in the comparison group. The clinical team
would therefore have to screen 820 individuals assuming a rate of infection of 20%, which was
found in previous pilot study work.
Among those screened we will calculate the prevalence of hepatitis C infection and the
severity of disease in this population compared with published data and risk factors for
chronic HCV infection and re-infection for those achieving SVR or test negative. We will also
investigate the proportion completing treatment and factors associated with better treatment
completion and SVR using multivariable regression models. Statistical software used in the
analysis will be STATA version 14.1.
(1) The HALT Study. Unpublished: http://www.isrctn.com/ISRCTN24707359
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03686722 -
Effect of Co-administration of Metformin and Daclatasvir on the Pharmacokinetis and Pharmacodynamics of Metformin
|
Phase 1 | |
Recruiting |
NCT04510246 -
Link Hepatitis C Notifications to Treatment in Tasmania
|
N/A | |
Completed |
NCT03413696 -
Effects of Health Literacy and HCV Knowledge on HCV Treatment Willingness in HIV-coinfected Patients
|
||
Completed |
NCT03118674 -
Harvoni Treatment Porphyria Cutanea Tarda
|
Phase 2 | |
Completed |
NCT03109457 -
Hepatitis C Virus Detection in Oral Squamous Cell Carcinoma
|
||
Completed |
NCT01458054 -
Effect of Omeprazole and Ritonavir on GSK2336805 Pharmacokinetics in Healthy Adults
|
Phase 1 | |
Completed |
NCT03740230 -
An Observational Study of Maviret (Glecaprevir/Pibrentasvir) for Korean Chronic Hepatitis C Genotypes 1 to 6 Patients According to the Standard for Re-examination of New Drugs
|
||
Completed |
NCT03426787 -
Helping Empower Liver and Kidney Patients
|
N/A | |
Completed |
NCT03627299 -
Renal Transplants in Hepatitis C Negative Recipients With Nucleic Acid Positive Donors
|
Phase 4 | |
Completed |
NCT00006301 -
Immune Response to Hepatitis C Virus
|
||
Active, not recruiting |
NCT03949764 -
The Kentucky Viral Hepatitis Treatment Study
|
Phase 4 | |
Completed |
NCT03365635 -
Administration of Zepatier (Grazoprevir Plus Elbasvir) in Chronic Hemodialysis (HD) Patients With Hepatitis C
|
Phase 4 | |
Recruiting |
NCT04405024 -
Pilot Study on the Feasibility of Systematic Hepatitis C Screening of Hospitalized Patients
|
N/A | |
Completed |
NCT04525690 -
Improving Inpatient Screening for Hepatitis C
|
N/A | |
Completed |
NCT04033887 -
Evaluation Study of RDTs Detecting Antibodies Against HCV
|
||
Withdrawn |
NCT04546802 -
HepATocellular Cancer Hcv Therapy Study
|
Phase 3 | |
Active, not recruiting |
NCT02961426 -
Strategic Transformation of the Market of HCV Treatments
|
Phase 2/Phase 3 | |
Completed |
NCT02869776 -
Integrating HCV and HIV Screening During the Era of HIV Antigen Testing
|
N/A | |
Completed |
NCT02705534 -
Sofosbuvir, Ledipasvir, Ribavirin for Hepatitis C Cirrhotics, Genotype 1
|
Phase 3 | |
Completed |
NCT02992184 -
PoC-HCV Genedrive Viral Detection Assay Validation Study
|
N/A |