Serological surveillance for SARS-CoV-2 = Faster, more accurate national tracking of the spread of COVID-19 - Serological surveillance for SARS-CoV-2 in the community, at-risk groups and Health Workers.
- Funded by Snow Medical via CREID
- Total publications:0 publications
Grant number: unknown
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Key facts
Disease
COVID-19start year
-99Known Financial Commitments (USD)
$0Funder
Snow Medical via CREIDPrincipal Investigator
Kristine Macartney, John Kaldor, Matthew O'SullivanResearch Location
AustraliaLead Research Institution
National Centre for Immunisation Research and Surveillance, Sydney Children?s Hospitals Network,University of Sydney The Kirby Institute, UNSW, University of Sydney and Westmead HospitalResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Immunity
Special Interest Tags
N/A
Study Type
Clinical
Clinical Trial Details
Not applicable
Broad Policy Alignment
Pending
Age Group
Adults (18 and older)Children (1 year to 12 years)Older adults (65 and older)
Vulnerable Population
Pregnant women
Occupations of Interest
Health Personnel
Abstract
The National Centre for Immunisation Research and Surveillance will coordinate collection of blood samples from all States and Territories to measure specific antibodies and provide more accurate tracking of COVID-19 spread in the elderly, close patient contacts, healthcare workers and identification of the level of virus in asymptomatic groups (pregnant women, children, workplace contacts). Objectives Estimate SARS-CoV-2 spread by determining immunity in the community and key risk groups (school-aged children, pregnant women, health care workers, older age groups living in the community and others) Undertake focussed sero-surveys in settings where community transmission has been occurring, such as Sydney and other capital cities and/or hot spots Calculate the incidence of SARS-CoV-2 seroconversion and assess factors associated with SARS-CoV-2 seroconversion among health care workers or laboratory personnel Determine the infection risk gradient between different professional groups, and in relation to types of exposure, types of personal protective equipment (PPE) worn and PPE compliance rates Obtain critical information for decision-making in response to COVID-19 over coming months and years. Research Plan Serological surveillance for SARS-CoV-2 in community groups Study Design: Non-randomised prospective observational cohort studies. National surveillance will be coordinated through the National Centre for Immunisation Research and Surveillance facilitated through national networks. Community members of all ages (but with oversampling for elderly and children) will be recruited to participate in national sero-surveys over two rounds. Pregnant women and people with medical risk conditions will also be invited to participate, recruited from prenatal clinics and immunology clinics, respectively. Study coordinators will be based at four sites with detection of SARS-CoV-2 antibodies at Westmead and Melbourne. Study Sites: Study sites: NCIRS Westmead, The Kirby Institute UNSW, Telethon Kids Institute WA and Red Cross Blood Service, Queensland Serological surveillance for SARS-CoV-2 in HCW Study Design: non-randomised prospective observational cohort study. Participants will, at monthly intervals (i) complete a questionnaire describing contact with individuals with suspected or proven COVID-19 or handling of laboratory samples from these individuals and (ii) have blood collected for detection of SARS-CoV-2 antibodies (iii) have nasal and oral swabs collected (selected participants) for virus detection. Study Sites: NSW and SA - Westmead Hospital, The Children's Hospital at Westmead, Royal North Shore Hospital, Blacktown Mt Druitt Hospital, Nepean Hospital, St Vincent's Hospital, Wagga Wagga Base Hospital, Royal Adelaide Hospital; VIC - Royal Melbourne Hospital, Austin Hospital, Monash Medical Centre, Bendigo Health; other state sites pending trajectory of the epidemic