Assessment of the Prevalence and the Impact of the COVID-19 Epidemic in the French Flight Crew in 2020 (Covaé)

The aeronautical community was also affected and greatly impacted economically and socially by the Covid-19 pandemic. Away from the acute phase, the epidemiological impact and the consequences of this disease within the French aviation flight crew population must be assessed. This study is aimed at providing original epidemiological data among civil and military aircrew, prior to possible prevention strategies or countermeasures to optimize risk management in terms of aviation safety and to promote, if necessary, future targeted studies.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

479

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Clamart, France, 92140
        • Centre d'Expertise Medicale du Personnel Navigant (CEMPN) de l'Hôpital d'Instruction des Armées Percy
      • Toulon, France, 83000
        • Centre d'Expertise Medicale du Personnel Navigant (CEMPN) de l'Hôpital d'Instruction des Armées Sainte-Anne

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The study population will be composed of professional military aircrew of all aeronautical specialties presenting themselves for a periodic medical exam.

Description

Inclusion Criteria:

  • At least 18 years of age
  • Professional military aircrew
  • Presenting himself/herself for a periodic medical exam

Exclusion Criteria:

  • Under 18 years of age
  • Parachutists
  • Non-professional aircrew
  • Presenting himself/herself for a first medical exam
  • Pregnant woman, parturient, breastfeeding

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prevalence of COVID-19 infection among French military professional aircrew
Time Frame: At enrollment
Prevalence of COVID-19 infection will be estimated on the basis of the replies to the questionnaire
At enrollment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Predictive factors of COVID-19 infection
Time Frame: At enrollment
Predictive factors of COVID-19 infection will be assessed using a top-down logistic regression model taking into account socio-demographic and occupational variables.
At enrollment
Techniques used for COVID-19 screening
Time Frame: At enrollment
Techniques used for COVID-19 screening will be estimated on the basis of the replies to the questionnaire (among participants who reported being tested for COVID-19)
At enrollment
Reasons for COVID-19 screening
Time Frame: At enrollment
Reasons for COVID-19 screening will be estimated on the basis of the replies to the questionnaire (among participants who reported being tested for COVID-19)
At enrollment
Experienced symptoms of COVID-19
Time Frame: At enrollment
Experienced symptoms of COVID-19 will be estimated on the basis of the replies to the questionnaire (among participants who reported being infected)
At enrollment
Medical care of COVID-19
Time Frame: At enrollment
Medical care of COVID-19 will be estimated on the basis of the replies to the questionnaire (among participants who reported being infected)
At enrollment
Social consequences of the COVID-19 pandemic
Time Frame: At enrollment
Social consequences of the COVID-19 pandemic will be estimated on the basis of the replies to the questionnaire
At enrollment
Factors associated with pejorative consequences of the COVID-19 pandemic
Time Frame: At enrollment
Factors associated with pejorative consequences of the COVID-19 pandemic will be assessed using a top-down logistic regression model taking into account socio-demographic and occupational variables.
At enrollment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2020

Primary Completion (Actual)

December 31, 2020

Study Completion (Actual)

December 31, 2020

Study Registration Dates

First Submitted

August 14, 2020

First Submitted That Met QC Criteria

August 14, 2020

First Posted (Actual)

August 17, 2020

Study Record Updates

Last Update Posted (Actual)

May 10, 2023

Last Update Submitted That Met QC Criteria

May 9, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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