- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04566198
Smoking in the Paris Fire Brigade and Comparison According to the Type of Service (Permanent or On-call)
Tobacco use is one of the world's leading preventable causes of disease and premature death, and the physician has a central role in detecting smokers and helping them to quit.
Tobacco use in the military undermines fitness, readiness and performance, and increases health care costs.
A study conducted on a French Army contingent on external operations in Afghanistan have shown an increase in tobacco use in situation of operational constraints (stress, shift work, etc.). However, another study conducted in Ivory Coast on a mobile gendarmerie squadron showed no significant difference.
Among the American firefighters who have been exposed to the 9/11 World Trade Center attacks, smoking have been shown to play an aggravating role in the recovery of lung function.
This study is aimed at assessing smoking prevalence in the Paris Fire Brigade, which is composed of young and healthy sportsmen and women who are exposed to strong operational constraints.
Study Overview
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Paris, France, 75017
- Centre Médical de Champerret
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Paris, France, 75020
- Antenne médicale de Ménilmontant
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- To be 18 years of age or older
- To be French
- To be an active military member
- To work in the Paris Fire Brigade
Exclusion Criteria:
- To be a civilian
- To be a reservist
- To be a foreigner
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Proportion of smokers
Time Frame: At enrollment (day 1)
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The smoking status (smoker or non-smoker) will be determined according to the responses to the questionnaire.
The proportion of smokers will be calculated by dividing the number of smokers by the total number of participants.
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At enrollment (day 1)
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Collaborators and Investigators
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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2019PPRC12
- 2020-A01843-36 (Other Identifier: IDRCB)
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
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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