Skip to content

Study of SARS-CoV2 Virus (COVID-19) Seroprevalence Among Lyon-Bron Military Health Schools Personnel

Study of SARS-CoV2 Virus (COVID-19) Seroprevalence Among Lyon-Bron Military Health Schools Personnel

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04516928
Acronym
SeroCovEms
Enrollment
392
Registered
2020-08-18
Start date
2020-09-21
Completion date
2020-09-25
Last updated
2021-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19, SARS-CoV Infection

Brief summary

Emerging in China in December 2019, Covid-19, whose pathogen is SARS-Cov-2, was declared a global pandemic in March 2020. The clinical presentation is highly variable, ranging from asymptomatic forms to acute respiratory distress and even death. Transmission is by droplet route, with an R0 of approximately 3. Rapidly, population protection measures were put in place by governments, including the confinement of all persons whose functions were not considered essential and the closure of educational institutions. Health care institutions are places at risk of Covid-19 transmission and hospital staff are particularly exposed, either through direct contact with patients, contact with exposed persons or through the environment. In order to protect personnel, hygiene measures were immediately recalled and reinforced. During the period of containment, the majority of students from the Lyon-Bron Military Medical Schools were sent as reinforcement in Army Training Hospitals and in the Military Reanimation Unit (Mulhouse). Some students developed symptomatic forms of SARS-Cov-2 infection, documented by positive PCR, during Operation Resilience or on their return from the mission. The Lyon-Bron Military Medical Schools staff, exposed both to the initial phase of the epidemic and to national protection measures, represent an extremely interesting population for understanding the epidemiological dynamics of the virus.

Interventions

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

OTHERQuestionnaire

A questionnaire on socio-demographical status, health status and lifestyle habits during the pandemic will be filled by the participants at Day 0.

Sponsors

Direction Centrale du Service de Santé des Armées
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* at least 18 years of age * personnel of the Military Health Schools of Lyon-Bron * working at the Military Health Schools of Lyon-Bron during the COVID-19 crisis

Exclusion criteria

* under 18 * contraindication to blood sampling

Design outcomes

Primary

MeasureTime frameDescription
Proportion of anti-SARS-CoV2 seropositive participantsDay 0The proportion of anti-SARS-CoV2 seropositive participants will be determined. ELISA serology test will be used to detect anti-SARS-CoV2 antibodies (IgG and IgM) at Day 0.

Secondary

MeasureTime frameDescription
Proportion of asymptomatic participants (among anti-SARS-CoV2 seropositive participants)Day 0The proportion of asymptomatic participants (among anti-SARS-CoV2 seropositive participants) will be determined. COVID-19 symptoms will be measured using a questionnaire.
Correlation coefficient between medical risk factors and a positive serologyDay 0Correlation coefficient between medical risk factors and a positive serology will be assessed using a step-by-step top-down regression analysis.
Correlation coefficient between epidemiological risk factors and a positive serologyDay 0Correlation coefficient between epidemiological risk factors and a positive serology will be assessed using a step-by-step top-down regression analysis.
Correlation coefficient between social risk factors and a positive serologyDay 0Correlation coefficient between social risk factors and a positive serology will be assessed using a step-by-step top-down regression analysis.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026