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EFFICACY OF A PHYSICAL ACTIVITY COACHING SYSTEM FOR PATIENTS WITH COPD (Effectiviteitsonderzoek naar een coachingsprogramma voor het behouden van fysieke activiteit in patienten met COPD)


- candidate number23336
- NTR NumberNTR5558
- ISRCTNISRCTN no longer applicable
- Date ISRCTN created
- date ISRCTN requested
- Date Registered NTR30-okt-2015
- Secondary IDsNL52206.100.15  
- Public TitleEFFICACY OF A PHYSICAL ACTIVITY COACHING SYSTEM FOR PATIENTS WITH COPD (Effectiviteitsonderzoek naar een coachingsprogramma voor het behouden van fysieke activiteit in patienten met COPD)
- Scientific TitleEFFICACY OF A PHYSICAL ACTIVITY COACHING SYSTEM FOR PATIENTS WITH COPD
- ACRONYM/
- hypothesisStudy 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.
- Healt Condition(s) or Problem(s) studiedCOPD, Physical activity, Support
- 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
- mec approval receivedyes
- multicenter trialyes
- randomisedyes
- masking/blindingNone
- controlActive
- groupParallel
- Type2 or more arms, randomized
- Studytypeintervention
- planned startdate 1-apr-2015
- planned closingdate1-apr-2016
- Target number of participants90
- InterventionsOne 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.
- 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
- Timepointsstart (8-16 week, inpatient) rehab; end rehab; and after 8 weeks at home.
- Trial web site/
- statusopen: patient inclusion
- CONTACT FOR PUBLIC QUERIES Marian Dekker
- CONTACT for SCIENTIFIC QUERIES Marian Dekker
- Sponsor/Initiator Philips Research Eindhoven, CIRO+ (Centre of expertise for chronic organ failure)
- Funding
(Source(s) of Monetary or Material Support)
Philips Research Eindhoven, CIRO+
- Publications
- Brief summaryStudy 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.
- Main changes (audit trail)
- RECORD30-okt-2015 - 4-feb-2016


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