Activity and heart rate monitor validation study
Completed
- Conditions
- Sedentary behavior, suboptimal physical fitness Sedentair gedrag, suboptimale lichamelijke fitheid
- Registration Number
- NL-OMON19960
- Lead Sponsor
- Joep RousHead of Product EngineeringPhilips Consumer Lifestyle, Personal Health SolutionsHigh Tech Campus 37 (HTC 37 1.008)5656AE Eindhoven+31 651490001
- Brief Summary
Planned, none accepted to date
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 31
Inclusion Criteria
Aged more than 18 years old . '
Body mass index [body weight (kilograms)] / [height^2 (meters)] between 19 and 35
Exclusion Criteria
Suffering from severe chronic disease for which a physician has contraindicated moderate intensity exercise without medical supervision
- Function/mobility and or cognitive impairments preventing compliance with the study protocol
Having pacemaker or other implantable electronic devices
Skin issues or wounds in wrist area
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method measurement accuracy of energy expenditure<br /><br>measurement accuracy of resting heart rate
- Secondary Outcome Measures
Name Time Method Secondary parameters include assessment of accuracy of other measures: <br /><br>- heartrate <br /><br>- sleep duration<br /><br>- steps counting <br /><br>- activity recognition <br /><br>- respiration rate at rest <br /><br>- sedentary behaviour alert <br /><br>- heart rate recovery<br /><br>- interbeat interval <br /><br>- VO2max estimation (yes/no) <br /><br>Additionally the wear comfort of the device will be evaluated with a questionnaire.