COVID19 U07.1
Conditions
Interventions
Group 1: Participants will be asked once about risk factors for severe courses of SARS-CoV-2 infection and their vaccination and recovery status.
Subsequently, a set for collecting a blood sample from
Sponsors
Institut für Virologie/Universitätsklinikum Bonn
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Randomised invitation based on participation in the payback panel - Randomised invitation for participation via telephone - Ability to answer a questionaire in german
Exclusion criteria
Exclusion criteria: None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the prevalence of anti-SARS/CoV-2 seropositive individuals in the study population, defined as the number of individuals with positive laboratory findings for S or N antibodies divided by the total number of study participants. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints are. (i) the "underdetection rate", defined as the number of individuals with a positive laboratory result (in the study) but without known prior exposure to SARS-CoV-2 (before the study was conducted), divided by the total number of study participants, (ii) the "vaccination underreporting rate," defined as the difference between the publicly reported vaccination rate and the study vaccination rate, which is the ratio of the reported vaccinations in the questionnaire to the total number of study participants. | — |
Countries
Germany
Contacts
Public ContactHendrik Streeck
Institut für Virologie/Universitätsklinikum Bonn
Outcome results
None listed