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Study of the Spread of COVID-19 in Saint Petersburg, Russia

E

European University at St. Petersburg

Status

Completed

Conditions

COVID19

Study type

Observational

Funder types

Other

Identifiers

NCT04406038
CDRU-001

Details and patient eligibility

About

Seroprevalence study of COVID-19 in Saint Petersburg, Russia is a regional longitudinal cohort study aiming to evaluate the spread dynamics of the COVID-19 disease in the population of Saint Petersburg. Clinically asymptomatic adults are sampled from the population using random digit dialing and tested for the presence of SARS-CoV-2-specific antibodies in the blood serum. Data collection and serial sampling of the same individuals spans four weeks and is conducted every two weeks in order to understand both the spread of the virus in the population.

Full description

At least 1 000 individuals, 18 years old and older, are randomly sampled using random digit dialing from the population of Saint Petersburg, Russia. Random sampling is performed by a survey company on the list of mobile phone numbers with designated geography prefixes of St. Petersburg. The baseline questionnaire for computer-assisted telephone interview includes travel history, medical history, and socio-economic status of the respondents. Sampled individuals are then invited to the clinic for blood sampling, their refusal to participate is recorded. Collected blood samples are used for SARS-CoV-2-specific antibodies testing. Data and sample collection spans four weeks and is conducted every two weeks. Participants complete additional questionnaires in the clinic providing information on medical history, history of allergies, chronic disease, smoking, and medication taken regularly. Contact tracing data and environmental conditions of the household are reсorded.

Enrollment

1,038 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Individuals sampled from the population of Saint Petersburg, Russia using random digit dialling.
  • Subjects aged 18 and older of both genders.
  • Asymptomatic at the time of blood draw.
  • Written informed consent for a blood draw, SARS-COV-2 antibody test, and data collection.

Exclusion criteria

  • Presence of fever or cough or respiratory distress at the time of blood test not attributable to other known chronic disease.
  • Age under 18.
  • Any health condition that may be a contraindication towards blood sampling in out-patient clinic.
  • Residence in Kolpinskiy, Kurortniy, Krasnoselsky, Kronshtadtskiy, Petrodvorcoviy, Pushkinskiy districts of St. Petersburg.

Trial design

1,038 participants in 1 patient group

Healthy adults
Description:
Healthy adults randomly sampled from the population of Saint Petersburg

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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