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NCT05577767 Clinical Trial

Does Longitudinal Nursing Follow-up Improve Smoking Cessation in Patients Referred for COPD Screening

COPD Clinical Trial

— BPCO  

Official title:
Does Longitudinal Nursing Follow-up Improve Smoking Cessation in Patients With Chronic Obstructive Pulmonary Disease (COPD) Screening

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05577767
Other study ID # 00008
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 11, 2020
Est. completion date September 11, 2026

Study information
Verified date December 2023
Source Centre Hospitalier de Valence
Contact Gilles RIVAL, MD
Phone +33(0)4 75 75 75 71
Email grival@ch-valence.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

a monocentric study to evaluate the efficacy of a longitudinal nursing follow up in smoking cessation in patients screened for Chronic obstructive pulmonary disease (COPD).

Description:

The challenges to limit the occurrence of COPD are early detection, the fight against smoking and smoking and addictions (e.g. Cannabis), as well as the fight against environmental exposures. we proposed to evaluate if a longitudinal nursing follow-up at 3 months, 6 months and one year, in patients coming to screening for COPD. Cessation of respiratory toxics is the most effective intervention in stopping the progression of COPD.

Recruitment information / eligibility
Status Recruiting
Enrollment 233
Est. completion date September 11, 2026
Est. primary completion date September 11, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Smoking patients screened for COPD between 35 years old 65 years old - Read, write and understand the French language - Patient affiliated to a social security system - Written and signed informed consent Exclusion Criteria: - Patients with a diagnosis of respiratory diseases - Patients receiving inhaled respiratory therapy - Persons unable to perform spirometry - Pregnant women - Refusal to participate in research - Patient under guardianship, deprived of liberty, safeguard of justice

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Ch Valence Valence Drome

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier de Valence

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary number of cigarettes or other toxic substances per day up to 1 year
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