Free-living assessment of Cardiorespiratory Fitness.
- Conditions
- niet-klinisch onderzoek met gezonde proefpersonennot applicable
- Registration Number
- NL-OMON37152
- Lead Sponsor
- Philips Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Men and women
Aged between 18-45 years
Body mass index between 18.5-27 kg/m2
Informed consent by the participants
Exclusion Criteria
Subjects with a chronic disease, such as chronic obstructive pulmonary disease, diabetes, cardiovascular disease or any condition known to affect normal cardiovascular functioning. Any musculoskeletal condition that would prevent the subject from perfoming the exercise protocol.
Subjects taking medication, except for oral contraceptives.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>• Maximal aerobic capacity (VO2max) as a measure of cardiorespiratory fitness<br /><br>as assessed by an incremental test on a bicycle ergometer.<br /><br>• Maximal aerobic capacity (VO2max) as a measure of cardiorespiratory fitness<br /><br>as estimated by a combination of heart rate recording and movement registration<br /><br>(accelerometry) in daily life.</p><br>
- Secondary Outcome Measures
Name Time Method <p>maximal heart rate<br /><br>resting heart rate<br /><br>heart rate recovery<br /><br>daily physical activity (accelerometer counts)<br /><br>body composition (% fat mass and fat-free mass)</p><br>