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Trial registered on ANZCTR
Registration number
ACTRN12621000996864
Ethics application status
Approved
Date submitted
15/07/2021
Date registered
28/07/2021
Date last updated
28/04/2024
Date data sharing statement initially provided
28/07/2021
Type of registration
Retrospectively registered
Titles & IDs
Public title
COVID-19 ANTibody And T-cell Assays
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Scientific title
A research study to develop new diagnostic tests to detect antibody and viral antigens for COVID-19 to identify those who may be immune and less likely to infect others.
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Secondary ID [1]
304481
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Nil Known
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Universal Trial Number (UTN)
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Trial acronym
The CANTATA Study
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
COVID-19
322316
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Condition category
Condition code
Infection
319987
319987
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0
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Other infectious diseases
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Respiratory
320479
320479
0
0
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Other respiratory disorders / diseases
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Intervention/exposure
Study type
Observational
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Patient registry
False
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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
Participants aged over 18 years entering New Zealand, or working at the borders and those who have had COVID-19 will be asked to provide blood and saliva sample at yearly intervals over a 3 year period. They will also be asked to complete a 10 minute health questionnaire and consent to follow of of their health by direct contact and remote access through the Ministry of Health, GP, District Health Board, Laboratory, Pharmaceutical, Births and Death & Marriages administrative records
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Intervention code [1]
320834
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Diagnosis / Prognosis
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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SARS-COV-2 Antibody prevalence assessed by blood sample
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Assessment method [1]
327861
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Timepoint [1]
327861
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At baseline
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Primary outcome [2]
327862
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SARS-COV-2 active T-cell prevalence assessed by blood sample
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Assessment method [2]
327862
0
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Timepoint [2]
327862
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At baseline
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Primary outcome [3]
327863
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Diagnosis of a cardiac condition as determined from data linkage to medical records
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Assessment method [3]
327863
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Timepoint [3]
327863
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2 years after baseline sampling
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Secondary outcome [1]
396801
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Duration of COVID-19 symptoms as assessed by medical history questionnaire
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Assessment method [1]
396801
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Timepoint [1]
396801
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2 years after baseline sampling
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Eligibility
Key inclusion criteria
Any person 18 years of age or older who has had 1) clinically verified COVID 19, 2) suspected of being exposed to SARS-COV-2, 3) close or casual associates of 1) or 2) and those coming into New Zealand via the quarantine and isolation facilities along with staff working at the borders or in health facilities will be invited to take part in this observational study.
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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
Unwilling to provide signed informed consent
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Study design
Purpose
Screening
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
Data will be entered into a dedicated database (STARLIMS, Abbott Informatics) throughout the conduct of the study, and extracted in a de-identified format to SPSS for statistical analysis. Levels of biomarkers and clinical indices will be assessed for normal distribution and, if appropriate, log-transformed to validate parametric analyses including t-tests. P<0.05 will be accepted as indicating significance.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
11/06/2021
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Date of last participant enrolment
Anticipated
30/06/2024
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Actual
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Date of last data collection
Anticipated
31/12/2027
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Actual
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Sample size
Target
3000
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Accrual to date
3
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Final
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Recruitment outside Australia
Country [1]
23781
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New Zealand
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State/province [1]
23781
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Funding & Sponsors
Funding source category [1]
308842
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Government body
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Name [1]
308842
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Ministry of Business Innovation and Employment
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Address [1]
308842
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15 Stout Street, Wellington 6011
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Country [1]
308842
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New Zealand
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Primary sponsor type
University
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Name
University of Otago
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Address
362 Leith Street
North Dunedin
Dunedin 9016
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Country
New Zealand
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Secondary sponsor category [1]
309758
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None
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Name [1]
309758
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Address [1]
309758
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Country [1]
309758
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
308749
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Southern Health and Disability Ethics Committee
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Ethics committee address [1]
308749
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Health and Disability Ethics Committees Ministry of Health 133 Molesworth Street PO Box 5013 Wellington 6011
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Ethics committee country [1]
308749
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New Zealand
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Date submitted for ethics approval [1]
308749
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17/12/2020
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Approval date [1]
308749
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10/05/2021
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Ethics approval number [1]
308749
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21/STH/12
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Summary
Brief summary
We will recruit up to 3000 participants including ideally 200-300 clinically proven COVID cases to assess 1) Antibody prevalence, performance and responses 2) active T-cell prevalence, responses and types 3) cardiac outcomes over the next 3 years in proven COVID cases versus “others”. Event rates will be obtained through Ministry of Health, GP, DHB, Birth Death & Marriages and phone or email follow up with participants. This will provide a biobank to draw upon for future investigator inspired work.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
111758
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Prof Chris Pemberton
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Address
111758
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Christchurch Heart Institute
Department of Medicine
University of Otago, Christchurch
PO Box 4345
Christchurch Central 8011
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Country
111758
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New Zealand
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Phone
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+643 33640887
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Fax
111758
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+643 364 1115
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Email
111758
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[email protected]
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Contact person for public queries
Name
111759
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Chris Pemberton
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Address
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Christchurch Heart Institute
Department of Medicine
University of Otago, Christchurch
PO Box 4345
Christchurch Central 8011
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Country
111759
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New Zealand
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Phone
111759
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+643 33640887
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Fax
111759
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+643 364 1115
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Email
111759
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[email protected]
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Contact person for scientific queries
Name
111760
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Chris Pemberton
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Address
111760
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Christchurch Heart Institute
Department of Medicine
University of Otago, Christchurch
PO Box 4345
Christchurch Central 8011
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Country
111760
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New Zealand
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Phone
111760
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+643 33640887
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Fax
111760
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+643 364 1115
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Email
111760
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
there is a no plan to make individual participant data (IPD) publicly available for this study
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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