- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04643444
Police COVID-19 Serosurvey (PoliCOV)
Police Officer COVID-19 Seroprevalence Survey in the Canton of Bern, Switzerland
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
i) To determine the extent of infection with seroprevalence data in the special population of police officers of the canton Bern.
ii) To determine risk factors for infection by comparing the proportion of seropositivity (infected versus noninfected individuals). The investigators hypothesize that police officers with fieldwork activity will have a higher seroprevalence than will office and administration personnel. The investigators hypothesize that working in the city of Bern will be associated with a higher seroprevalence than will working in other geographic areas of the canton (i.e. rural area).
iii) To monitor COVID-19 antibody titres and neutralizing capacity over time and to associate them with reinfection rates and infection-free intervals in police officers after accidental contact with a proven COVID-19 case. The investigators hypothesize that in seropositive individuals, there will be a decreasing dynamic of antibody titres over the one-year study period, and hence, a decrease of neutralizing capacity.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Canton of Bern
-
Bern, Canton of Bern, Switzerland, 3010
- University of Bern, Institute for Infectious Diseases
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Police officers of the cantonal police of Bern volunteering to participate in the study.
Exclusion Criteria:
- Refusal or inability to give informed consent or contraindication to venepuncture.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Seroprevalence
Time Frame: One year
|
The variable of primary interest is COVID-19 seropositivity.
This variable is measured at five time points over the one-year study period.
The following baseline factors may have an influence on the primary endpoint and will be obtained: (i) pre-existing comorbidities, (ii) rural versus city distribution of working place, and (iii) office work versus field work.
|
One year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Risk profile assessment
Time Frame: One year
|
The investigators will assess the proportion of symptomatic and asymptomatic cases among seropositive participants.
The investigators will calculate the attack rate in different subgroup.
These include (i) study participants with health-related risk factors (age>50 and age>60 years, diabetes, arterial hypertension, cardiovascular disease, chronic pulmonary disease, immune-compromised status due to host diseases, medical treatment, cancer, obesity), (ii) activity-related subgroups (i.e.
fieldwork vs office activity), (iii) geography-related subgroups (i.e.
city vs rural areas).
In follow-up visits, the antibody titers (i.e.
dynamic) and the neutralization capacity will be assessed.
Thereby, the investigators will determine the change in serum levels of SARS-CoV-2 antibodies over time in seropositive participants.
|
One year
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Parham Sendi, MD, University of Bern
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Respiratory Tract Infections
- Infections
- RNA Virus Infections
- Virus Diseases
- Respiratory Tract Diseases
- Lung Diseases
- Pneumonia, Viral
- Pneumonia
- Coronavirus Infections
- Coronaviridae Infections
- Nidovirales Infections
- COVID-19
- Investigative Techniques
- Specimen Handling
- Clinical Laboratory Techniques
- Diagnostic Techniques and Procedures
- Diagnosis
- Punctures
- Surgical Procedures, Operative
- Blood Specimen Collection
Other Study ID Numbers
- 2020-02650
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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