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Validation of French Version of LCADL and Dyspnea-12

Completed
Conditions
Copd
Registration Number
NCT02555202
Lead Sponsor
University Hospital, Brest
Brief Summary

The main objective of this study is to develop and to validate a French version of the London Chest Activity of Daily Living (LCADL) and the Dyspnea 12 and to determine the reliability of this version for the evaluation of the dyspnea in the Activity of Daily Living in COPD patients (stages severe and very severe).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria
  • COPD with FEV1< 50% of predictive value
Exclusion Criteria
  • FEV1> 50% of predictive value
  • Patients with an exacerbation of COPD in the previous 30 days the inclusion

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
the Saint-Georges questionnaire, item Activity15 days

by comparison with item activities of the Saint-Georges questionnaire for the LCADL

MMRC Dyspnea scale15 days

by comparison with MMRC dyspnea scale for the dyspnea 12

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Brest University hospital

🇫🇷

Morlaix, France

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