chronic bronchitis Chronic Obstructie Pulmonary Disease (COPD)
Conditions
Interventions
Patients will be allocated either to the intervention group (using a hand-held
mechanical oPEP device) or the control group (using the sham version of the
hand-held device). Patients in both groups
Sponsors
Martini Ziekenhuis
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: clinical diagnosis of COPD or chronic bronchitis (aged 40 years or older) patients with sputum production/excess mucus informed consent
Exclusion criteria
Exclusion criteria: diagnosis of CF or bronchiectasis OPEP use in the past
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Respiratory symptoms as measured by the Clinical COPD Questionnaire (CCQ). | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are subdomainscores of the CCQ, health-related Quality of Life (SGRQ), cough symptoms (LCQ), global rating of change in health status and ability of coughing up sputum, lung function (FEV1 and FVC (L and % predicted)) and exacerbations. In addition data on adherence and patient satisfaction will be collected. | — |
Countries
Netherlands
Outcome results
None listed