Pulmonary RehabIlitation with Nasal-high-flow-support in COPD and Effectiveness: The PRINCE study
- Conditions
- Chronic Obstructive Pulmonary Disease (COPD)
- Registration Number
- NL-OMON24905
- Lead Sponsor
- CIRO+ Horn
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
Patients with COPD with hypoxia which at least demand 1 liter oxygen/min during baseline.
-Clinical stable on the basis of clinical picture by the chest physician.
Exclusion Criteria
-Lack of motivation for voluntary participation in the present study.
-Outpatient pulmonary rehabilitation program in a hospital which is part of the CIRO network.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The main study parameter is the increase in cycle endurance time after pulmonary rehabilitation.
- Secondary Outcome Measures
Name Time Method Secondary study parameters are changes in 6-min walking distance (6MWD), increase in training intensity, oxygen saturation, heart rate, Borg scores for dyspnoea and fatigue, lung function, health status and the number of exacerbations and hospitalizations. Long term outcome measures for the follow-up period are lung function, cycle endurance time, daily symptoms and the number of exacerbations and hospitalizations.