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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT05042544
Registration number
NCT05042544
Ethics application status
Date submitted
20/08/2021
Date registered
13/09/2021
Date last updated
13/06/2024
Titles & IDs
Public title
The National Australian HCV Point-of-Care Testing Program
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Scientific title
The National Australian HCV Point-of-Care Testing Program: An Observational Cohort Study to Evaluate the Use of Finger-stick Point-of-care Hepatitis C Testing to Enhance Diagnosis and Treatment of HCV Infection
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Secondary ID [1]
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VHCRP2101
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Hepatitis C
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Condition category
Condition code
Infection
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Other infectious diseases
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Oral and Gastrointestinal
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Intervention/exposure
Study type
Observational [Patient Registry]
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Diagnosis / Prognosis - Point-of-Care Testing
People at risk of HCV acquisition - This is an observational cohort study. Participants will be recruited from settings that provide services to people with a risk factor for the acquisition of HCV infection. Participants will attend a single visit to receive point-of-care HCV testing and complete a self-administered survey. Testing will be performed using point-of-care HCV antibody testing (results within 1-20 minutes, depending on the test) and if positive, HCV RNA testing will be performed. Participants who have previously had HCV infection or previously received HCV treatment will be tested using point-of-care HCV RNA testing. Participants will not receive treatment as a part of this study. Participants who are HCV RNA detectable will be linked to standard of care for any other clinical assessments and treatment initiation.
Diagnosis / Prognosis: Point-of-Care Testing
Participants will be offered finger-stick point-of-care testing for HCV
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Intervention code [1]
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Diagnosis / Prognosis
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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To evaluate the proportion of HCV infected (HCV RNA quantifiable) participants who initiate HCV treatment at 12 weeks following HCV RNA testing.
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Assessment method [1]
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HCV treatment
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Timepoint [1]
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12 Weeks from enrolment
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Secondary outcome [1]
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To evaluate the proportion of people who accept point-of-care testing among those offered testing.
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Assessment method [1]
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Accepting testing
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Timepoint [1]
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Recruitment phase
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Secondary outcome [2]
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To evaluate the prevalence of current HCV infection (HCV RNA quantifiable) among people tested.
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Assessment method [2]
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Prevalence
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Timepoint [2]
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Recruitment phase
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Secondary outcome [3]
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To evaluate the time to HCV treatment uptake among HCV RNA detectable participants following HCV RNA testing
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Assessment method [3]
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Time to treatment
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Timepoint [3]
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52 weeks
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Secondary outcome [4]
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To evaluate the proportion of HCV RNA detectable participants who initiate HCV treatment at 12 months (52 weeks) following detectable finger-stick point-of-care HCV RNA testing.
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Assessment method [4]
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Initiation of treatment
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Timepoint [4]
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52 weeks
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Secondary outcome [5]
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To evaluate the proportion of participants who complete HCV direct-acting antiviral (DAA) treatment.
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Assessment method [5]
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Completion of treatment
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Timepoint [5]
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52 weeks
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Secondary outcome [6]
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To evaluate the proportion of participants who achieve an SVR (defined as HCV RNA below the lower limit of quantitation at post treatment week 12) following a detectable HCV RNA test result.
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Assessment method [6]
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SVR
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Timepoint [6]
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12 weeks
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Secondary outcome [7]
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To evaluate the proportion of participants who are HCV RNA negative at 12 months (52 weeks) following a detectable HCV RNA test.
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Assessment method [7]
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HCV negative
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Timepoint [7]
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52 weeks
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Secondary outcome [8]
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To evaluate the cost-effectiveness of different testing strategies
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Assessment method [8]
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Cost-effectiveness
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Timepoint [8]
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52 weeks
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Eligibility
Key inclusion criteria
1. Provided informed consent.
2. = 18 years of age.
3. Have a risk factor for the acquisition of HCV infection (including current or past injecting drug use, previous incarceration, HIV infection, receiving blood products prior to 1990, having a tattoo or piercing in an unregulated environment, a needle-stick injury, or a mother with HCV).
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4. Are attending a service caring for people with risk factors for the acquisition of HCV infection (e.g. drug treatment clinics, needle and syringe programs, prisons, mobile outreach services, community health services, mental health services, and homelessness services).
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
a. Is unable or unwilling to provide informed consent or abide by the requirements of the study.
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
22/02/2022
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
1/12/2026
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Actual
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Sample size
Target
40000
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,NT,QLD,SA,TAS,VIC,WA
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Recruitment hospital [1]
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Hepatitis ACT - Canberra
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Recruitment hospital [2]
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Western NSW LHD - Bathurst
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Recruitment hospital [3]
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Far West LHD - Broken Hill
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Recruitment hospital [4]
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Maari Ma Health Aboriginal Corporation - Broken Hill
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Recruitment hospital [5]
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Galambila Aboriginal Health Service - Coffs Harbour
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Recruitment hospital [6]
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Central Coast LHD - Gosford
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Recruitment hospital [7]
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Armajun Health Service Aboriginal Corporation - Inverell
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Recruitment hospital [8]
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Rekindling the Spirit Health Service - Lismore
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Recruitment hospital [9]
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Nepean Blue Mountains LHD - Penrith
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Recruitment hospital [10]
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North and Mid North Coast LHD - Port Macquarie
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Recruitment hospital [11]
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Walhallow Aboriginal Corporation - Quirindi
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Recruitment hospital [12]
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Bulgarr Ngaru Medical Aboriginal Corporation - South Grafton
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Recruitment hospital [13]
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Kirketon Road Centre - Sydney
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Recruitment hospital [14]
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NSLHD - Sydney
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Recruitment hospital [15]
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WSLHD Drug Health - Sydney
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Recruitment hospital [16]
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South West Sydney LHD - Sydney
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Recruitment hospital [17]
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Hepatitis NSW - Sydney
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Recruitment hospital [18]
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NSW Users and AIDS Association - Sydney
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Recruitment hospital [19]
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Prince of Wales Hospital - Sydney
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Recruitment hospital [20]
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SESLHD Community and Mental Health POCT Allicance (SCAMPA) - Sydney
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Recruitment hospital [21]
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SESLHD Drug Health - Sydney
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Recruitment hospital [22]
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Storr Liver Clinic (Westmead Hospital) - Sydney
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Recruitment hospital [23]
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Sydney Local Health District - Sydney
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Recruitment hospital [24]
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Murrumbidgee & Southern LHD - Wagga Wagga
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Recruitment hospital [25]
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Hunter New England LHD - Waratah
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Recruitment hospital [26]
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ISLHD Drug and Alcohol Service - Wollongong
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Recruitment hospital [27]
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ADSCA - Alice Springs Hospital - Alice Springs
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Recruitment hospital [28]
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Alcohol and Harm Reduction Biala - Brisbane
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Recruitment hospital [29]
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Micah Projects - Brisbane
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Recruitment hospital [30]
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Cairns Sexual Health Service - Cairns
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Recruitment hospital [31]
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Hepatitis QLD - Coorparoo
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Recruitment hospital [32]
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Kombi Clinic - Inala
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Recruitment hospital [33]
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Metro South Addiction Services - Inala ADS - Inala
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Recruitment hospital [34]
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Ipswich AODS - Ipswich
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Recruitment hospital [35]
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Ipswich Sexual Health and BBV Service, West Moreton Health - Ipswich
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Recruitment hospital [36]
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OneBridge - Maroochydore
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Recruitment hospital [37]
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Central Adelaide Local Health Network - Adelaide
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Recruitment hospital [38]
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Drug and Alcohol Services South Australia - Adelaide
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Recruitment hospital [39]
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North Adelaide Local Health Network - Adelaide
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Recruitment hospital [40]
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South Adelaide Local Health Network - Adelaide
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Recruitment hospital [41]
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Hepatitis SA - Hackney
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Recruitment hospital [42]
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Pangula Mannamurna Aboriginal Corporation - Mount Gambier
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Recruitment hospital [43]
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Clinic 60 (Sexual Health Services) - Hobart
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Recruitment hospital [44]
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Moreton Group Rural Health - New Town
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Recruitment hospital [45]
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Western Health - Footscray
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Recruitment hospital [46]
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Eastern Health - Melbourne
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Recruitment hospital [47]
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St Vincent's Hospital (Melbourne) - Melbourne
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Recruitment hospital [48]
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Youth Projects - The Living Room - Melbourne
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Recruitment hospital [49]
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Latrobe Community Health Service Liited - Morwell
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Recruitment hospital [50]
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Peer Based Harm Reduction Bunbury - Bunbury
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Recruitment hospital [51]
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South Terrace Clinic - Fremantle Hospital - Fremantle
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Recruitment hospital [52]
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Peer Based Harm Reduction WA - Perth
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Recruitment hospital [53]
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Hepatitis WA - Perth
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Recruitment hospital [54]
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Next Step East Perth - Perth
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Recruitment hospital [55]
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Next Step Fremantle - Perth
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Recruitment hospital [56]
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Next Step Warwick - Perth
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Recruitment postcode(s) [1]
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2612 - Canberra
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Recruitment postcode(s) [2]
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2795 - Bathurst
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Recruitment postcode(s) [3]
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- Broken Hill
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Recruitment postcode(s) [4]
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- Coffs Harbour
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Recruitment postcode(s) [5]
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2250 - Gosford
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Recruitment postcode(s) [6]
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- Inverell
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Recruitment postcode(s) [7]
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- Lismore
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Recruitment postcode(s) [8]
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- Penrith
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Recruitment postcode(s) [9]
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2444 - Port Macquarie
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Recruitment postcode(s) [10]
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- Quirindi
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Recruitment postcode(s) [11]
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- South Grafton
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Recruitment postcode(s) [12]
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2010 - Sydney
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Recruitment postcode(s) [13]
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2065 - Sydney
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Recruitment postcode(s) [14]
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2151 - Sydney
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Recruitment postcode(s) [15]
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2170 - Sydney
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Recruitment postcode(s) [16]
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- Sydney
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Recruitment postcode(s) [17]
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- Wagga Wagga
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Recruitment postcode(s) [18]
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- Waratah
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Recruitment postcode(s) [19]
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- Wollongong
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Recruitment postcode(s) [20]
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- Alice Springs
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Recruitment postcode(s) [21]
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4000 - Brisbane
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Recruitment postcode(s) [22]
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4101 - Brisbane
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Recruitment postcode(s) [23]
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4870 - Cairns
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Recruitment postcode(s) [24]
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- Coorparoo
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Recruitment postcode(s) [25]
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4077 - Inala
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Recruitment postcode(s) [26]
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4305 - Ipswich
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Recruitment postcode(s) [27]
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4560 - Maroochydore
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Recruitment postcode(s) [28]
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5000 - Adelaide
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Recruitment postcode(s) [29]
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5069 - Adelaide
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Recruitment postcode(s) [30]
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5112 - Adelaide
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Recruitment postcode(s) [31]
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5168 - Adelaide
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Recruitment postcode(s) [32]
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5069 - Hackney
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Recruitment postcode(s) [33]
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- Mount Gambier
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Recruitment postcode(s) [34]
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- Hobart
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Recruitment postcode(s) [35]
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- New Town
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Recruitment postcode(s) [36]
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3011 - Footscray
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Recruitment postcode(s) [37]
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3128 - Melbourne
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Recruitment postcode(s) [38]
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- Melbourne
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Recruitment postcode(s) [39]
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3840 - Morwell
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Recruitment postcode(s) [40]
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6230 - Bunbury
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Recruitment postcode(s) [41]
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- Fremantle
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Recruitment postcode(s) [42]
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6230 - Perth
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Recruitment postcode(s) [43]
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- Perth
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Funding & Sponsors
Primary sponsor type
Government body
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Name
Kirby Institute
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Address
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Country
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Other collaborator category [1]
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Other
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Name [1]
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Flinders University
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
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Summary
Brief summary
The National Australian HCV Point-of-Care Testing Program will establish an observational cohort to evaluate whether scale-up of finger-stick point-of-care HCV testing increases diagnosis and treatment for HCV infection. Participants will be recruited from settings providing services to people with a risk factor for the acquisition of HCV infection (including drug treatment clinics, needle and syringe programs, homelessness settings, mental health services, prisons, and mobile outreach). Participants will attend a single visit to have their HCV RNA status tested and complete a self-administered survey. Participants will not receive treatment as a part of this study. Participants who are HCV RNA positive will be linked to standard of care.
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Trial website
https://clinicaltrials.gov/study/NCT05042544
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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David C Silk, BSc
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Address
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Country
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Phone
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+61293850900
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Fax
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Email
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[email protected]
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT05042544
Download to PDF