Pulmonary RehabIlitation with Nasal-high-flow-support in COPD and Effectiveness: The PRINCE study
- Conditions
- chronic bronchitisEmphysema10006436
- Registration Number
- NL-OMON46686
- Lead Sponsor
- CIRO+ Horn
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
- - 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.
- Documented desaturation during exercise, which demands at least 2 liters oxygen/min to correct.
- Permission for voluntary participation. Patient will be asked during the start of their rehabilitation program and have to sign an informed consent. Patients have the right to withdraw from the study without any negative consequences on their rehabilitation.
- Attending the regular rehabilitation program in CIRO+.
- Lack of motivation for voluntary participation in the present study.
- Not capable to understand the instruction of the NHF oxygen delivery system
- Outpatient pulmonary rehabilitation program in a hospital which is part of the CIRO network.
- Not capable to perform cycle tests, walk tests and/or endurance training on a cycle ergometer and treadmill.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method