Study of SARS-CoV2 Virus (COVID-19) Seroprevalence in the Population of Creil Air Force Base (BA110)

NCT ID: NCT04404270

Last Updated: 2021-07-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1146 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-05-26

Study Completion Date

2021-03-13

Brief Summary

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In mid-February 2020, within the Oise (France) cluster, a case of COVID-19 disease caused by a SARS-CoV2 infection was described among the personnel of the Creail Air Force Base (BA110). This resulted in the beginning of an epidemic controlled by epidemiological measures. One month later, containment measures were taken at the national level, measures that also applied to BA110 personnel. These personnel, exposed to both the initial phase of the epidemic and national protection measures, represent an extremely interesting population for understanding the epidemiological dynamics of the virus, particularly at a time when France is lifting the containment measures. It becomes extremely important to understand the levers of viral spread in order to adjust the health measures to be maintained as best as possible.

The main objective of this study is to determine the extent of virus diffusion in this highly circulating population, as evidenced by several identified cases of COVID-19.

Detailed Description

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Conditions

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Sars-CoV2

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Anti-SARS-CoV2 Serology

The anti-SARS-CoV2 serological status will be measured on a blood sample collected at Day 0.

Intervention Type DIAGNOSTIC_TEST

Questionnaire

Epidemiological data will be collected in a questionnaire that will be filled by participants at Day 0 (Visit 1), after 3 months (Visit 2) and after 9 months (Visit 3).

The questionnaire includes:

* medical data (height, weight, smoking, history of intense stress);
* socio-demographic data (age, gender, civil/military status, function/occupation, rank category, army, family status/home composition, housing conditions, etc.);
* clinical data : history of symptoms suggestive of COVID-19 in the last 3 months, current symptoms suggestive of COVID-19;
* use of care, hospitalization, work stoppage in the last 3 months;
* contact with people who are symptomatic or proven COVID-19.

Intervention Type BEHAVIORAL

Anti-SARS-CoV2 serological controls and serum neutralization

Serological controls and a serum neutralization test will be performed on blood samples collected 3 months (Visit 2) and 9 months (Visit 3) after Day 0, respectively.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Active military or civilian defence personnel working on the Creil Air Force Base (BA110) during the period of interest (from February 1st 2020 to the end of the study)

Exclusion Criteria

* Contraindication to blood sampling
* Pregnant, parturient, breastfeeding woman
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Direction Centrale du Service de Santé des Armées

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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24e antenne médicale de Creil

Creil, , France

Site Status

Countries

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France

Other Identifiers

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2020-A01368-31

Identifier Type: OTHER

Identifier Source: secondary_id

2020-COVID19-22

Identifier Type: -

Identifier Source: org_study_id

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