Inspiratory Muscle Training During Pulmonary Rehabilitation in COPD
Not Applicable
Completed
- Conditions
- Chronic Obstructive Pulmonary Disease
- Registration Number
- NCT02074813
- Lead Sponsor
- University Hospital, Brest
- Brief Summary
Demonstrate that IMT associated with a conventional pulmonary rehabilitation program allows a significant improvement of dyspnea in subjects with severe or very severe COPD than a conventional pulmonary rehabilitation program alone.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
- Patients with COPD stage 3 or 4
- Hospitalized in the pulmonary rehabilitation unit in the hospital of Morlaix, with a 3 weeks pulmonary rehabilitation course;
Exclusion Criteria
- FEV ≥ 50%
- Pneumonectomy, Lobectomy less than 6 months
- Patient with risk of spontaneous pneumothorax or rib fracture
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Dyspnea measure 21 - 4 days / +7 jours Measure of dyspnea with the Multidimensional Dyspnea Profile (MDP) questionnaire.
- Secondary Outcome Measures
Name Time Method PI max variation 21 - 4 days / +7 days Measure of PI max variation with MicroRPM
CI variation 21 - 4 days / +7 days Measure of CI variation with spirobank II
Dyspnea measure 21 - 4 days / +7 days Meausre of dyspnea with London Chest of Activity Daily Living (LCADL)
Trial Locations
- Locations (2)
Centre des maladies respiratoires et allergiques - Les Acacias
🇫🇷Briançon, France
Brest University Hospital
🇫🇷Morlaix, France
Centre des maladies respiratoires et allergiques - Les Acacias🇫🇷Briançon, France