Screening for Obstructive Respiratory Disorders in the General Population During the "Mai Poumon 2026" Prevention Campaign: Prevalence and Impact on the Care Pathway

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier de la côte Basque

About this trial

Undiagnosed COPD represents a significant issue in terms of morbidity and mortality, as nearly 50% of smokers with chronic respiratory symptoms also experience impaired quality of life and acute events similar to COPD exacerbations. We aim to study the prevalence of airflow obstruction (AO) and PRISm (preserved ratio impaired spirometry) in the general population.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years

Participating to the prevention campain "Mai Poumons 2026" on 09 Mai 2026

Disqualifiers

Contre-indication to perform a spirometry : hemoptysy, pneumothorax, myocardal infarction <1month, thoracic anevrism, recent ophtalmologic, abdominal or thoracic surgery

Unable to perform a spirometry (understanding, coordination)

Patient under legal protection

Patient pregnant or breasting

Trial population

Population attending the "9 Mai Poumon 2026" prevention campaign

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Spirometry

    Diagnostic test

    Spirometry to identify airflow obstruction and PRISm (Preserved ration impaired spirometry)

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Prevalence of newly diagnosed airflow obstruction (AO) and PRISm (preserved ratio impaired spirometry) in the general population

Percentage of AO and PRISm detected

Time frame
On the day of inclusion

Secondary outcomes

1

Description of the clinical characteristics of patients with and without Airflow Obstruction / with and without PRISm

Percentage of presence of symptoms, specific treatment

Time frame
At the day of inclusion
2

Description of the population participating to the prevention campaing

Percentage of presence of tabagism

Time frame
At the day of inclusion
3

Evaluation of the number of patients diagnosed with airflow obstruction or Prism and who attend a consult with a medical doctor after the prevention campain

Percentage of patients with a medical follow-up at 6 months

Time frame
At Month 6

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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