No registrations found.
ID
Source
Brief title
Health condition
COPD patients (Chronic Obstructive Pulmonary Disease); Physical activity; coaching; pulmonary rehabilitation
Sponsors and support
Intervention
Outcome measures
Primary outcome
-Physical activity
-Psycho-social factors by several questionnaires (e.g., anxiety, depression, self efficacy, responses to physical activity, motivation, personality, mood, clinical control variables).
-possible other explanatory factors for differences in physical activity, such as commonly used transport, having a dog, home settings (how do you live?), and exacerbation history.
Secondary outcome
-Evaluate the acceptance and usability of COPD patients to use an electronic physical activity coaching program at home by a short interview and google analytics
Background summary
Study physical activity of COPD patients before, during, and after pulmonary rehabilitation. Evaluate if the physical activity coaching system, designed by Philips Research, can support the maintenance of physical activity of COPD patients at home after pulmonary rehabilitation, compared to a control group without receiving physical activity coaching at home, and without receiving insight into their physical activities during the whole study.
Study objective
Study physical activity of COPD patients before, during, and after pulmonary rehabilitation. Evaluate if the physical activity coaching system, designed by Philips Research, can support the maintenance of physical activity of COPD patients at home after pulmonary rehabilitation, compared to a control group without receiving physical activity coaching at home, and without receiving insight into their physical activities during the whole study.
Study design
start (8-16 week, inpatient) rehab; end rehab; and after 8 weeks at home.
Intervention
One group (group 1; experimental group) of subjects receive physical activity insight & coaching after pulmonary rehabilitation by the developed Philips physical activity coaching system. The other group (group 2; control) only wears the activity monitor, without receiving coaching, and without receiving insight into their physical activities.
Inclusion criteria
• Age > 45 years;
• 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 before the start of the study;
• Absence of recent Myocardial Infarction (within last 3 months), unstable angina, other significant cardiac problems, resting SBP > 180 mmHg, resting DBP > 100 mmHg or tachycardia;
• Absence of significant orthopaedic, neurological, cognitive and/or psychiatric impairment restricting mobility.
• Internet Access at home.
Exclusion criteria
• 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
• 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 biomechanical 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
Design
Recruitment
Followed up by the following (possibly more current) registration
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL5277 |
| NTR-old | NTR5558 |
| CCMO | NL52206.100.15 |
| OMON | NL-OMON47200 |