Efficacy of a physical activity coaching system for patients with COPD
- Conditions
- chronic obstructive pulmonary disease10010613
- Registration Number
- NL-OMON47200
- Lead Sponsor
- Philips Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
* Age > 45
* Clinical diagnosis of COPD according to Global Initiative for Chronic Obstructive Lung Disease (GOLD)1 referred for pulmonary rehabilitation;
* Physically and mentally capable to cooperate
* Sufficient understanding of the Dutch language
* Clinical stability concerning pulmonary infections or acute exacerbations within last four weeks;
* Absence of recent Myocardial Infarction (within last 3 months), unstable angina, other significant cardiac problems, SBP > 180 mmHg, DBP > 100 mmHg or tachycardia;
* Absence of significant orthopaedic, neurological, cognitive and/or psychiatric impairment restricting mobility;
* Internet access at home.
* Subjects who do not meet the above mentioned inclusion criteria
* Subjects who are not primarily diagnosed with COPD
* Subjects unwilling or unable to sign the informed consent form (if applicable)
* Subjects with any significant disorder or disease other than COPD expected to significantly interfere with the study
* Subjects with orthopaedic, neurological or other complaints that significantly impair normal biome-chanical movement patterns, as judged by the investigator;
* Subjects with respiratory diseases other than COPD (e.g. asthma);
* Subjects with COPD exacerbations within 4 weeks prior to Visit 1;
* Subjects with cognitive impairment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary endpoint of the study is physical activity data measured by the<br /><br>activity monitor. </p><br>
- Secondary Outcome Measures
Name Time Method