Seroprevalence and immunity of SARS-CoV-2 infection in children and adolescents in schools in Switzerland: design for a longitudinal, school-based prospective cohort study
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Abstract
Objectives
This longitudinal cohort study aims to assess the extent and patterns of seroprevalence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibodies in school-attending children, and their parents and school personnel. It will examine risk factors for infection, the relationship between seropositivity and symptoms, and temporal persistence of antibodies.
Methods
The study ( Ciao Corona ) will enroll a regionally representative, random sample of schools in the canton of Zurich, where 18% of the Swiss population live. Children aged 5–16 years, attending primary and secondary schools, and their parents and school personnel are invited. Venous blood and saliva samples are collected for serological testing in June/July 2020, in October/November 2020, and in March/April 2021. Bi-monthly questionnaires will cover SARS-CoV-2 symptoms and tests, health, preventive behavior, and lifestyle information. Hierarchical Bayesian logistic regression models will account for sensitivity and specificity of the serological tests in the analyses and complex sampling structure, i.e., clustering within classes and schools.
Results and conclusions
This unique school-based study will allow describing temporal trends of immunity, evaluate effects of preventive measures and will inform goal-oriented policy decisions during subsequent outbreaks.
Trial registration ClinicalTrials.gov Identifier: NCT04448717, registered June 26, 2020. https://clinicaltrials.gov/ct2/show/NCT04448717 .
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SciScore for 10.1101/2020.08.30.20184671: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement IRB: Ethical aspects: The study was approved by the Cantonal Ethics Committee Zurich (
Consent: Written informed consent is obtained from parents or legal guardians (referred to as parents further on) of participating childrenRandomization Study overview, design and population: Study design: This is a longitudinal, population-based observational study in a regionally-representative cohort of children and adolescents from randomly selected schools and classes in the canton of Zurich, Switzerland. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
Antibodies Sentences Resources The ABCORA test (version 2.0) … SciScore for 10.1101/2020.08.30.20184671: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement IRB: Ethical aspects: The study was approved by the Cantonal Ethics Committee Zurich (
Consent: Written informed consent is obtained from parents or legal guardians (referred to as parents further on) of participating childrenRandomization Study overview, design and population: Study design: This is a longitudinal, population-based observational study in a regionally-representative cohort of children and adolescents from randomly selected schools and classes in the canton of Zurich, Switzerland. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
Antibodies Sentences Resources The ABCORA test (version 2.0) provides a highly differentiated picture of the immune response: immunoglobulins G (IgG), M (IgM) and A (IgA) antibodies against four SARS-CoV-2 targets (receptor binding domain (RBD), spike proteins S1 and S2), and the nucleocapsid protein (N) of SARS-CoV-2) are analyzed, resulting in twelve analyzed parameters. IgA) antibodies against four SARS-CoV-2 targets (receptor binding domain (RBD)suggested: NoneS2suggested: NoneResults from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).
Results from LimitationRecognizer: An explicit section about the limitations of the techniques employed in this study was not found. We encourage authors to address study limitations.Results from TrialIdentifier: We found the following clinical trial numbers in your paper:
Identifier Status Title NCT04448717 Recruiting Longitudinal Study of Seroprevalence of SARS-CoV-2 Antibodie… Results from Barzooka: We did not find any issues relating to the usage of bar graphs.
Results from JetFighter: We did not find any issues relating to colormaps.
Results from rtransparent:- Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
- No funding statement was detected.
- No protocol registration statement was detected.
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