Activity and heartrate monitor validation study

Completed

• Conditions: 10082206; Sedentary behavior; 10003018; Validatie meeteigenschappen van activiteiten en hartslagmonitor bij gezonde proefpersonen; suboptimal physical fitness

• Registration Number: NL-OMON43960
• Lead Sponsor: Philips

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 11 June 2024

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
- Functionally capable

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
- Might be, or is, pregnant

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary parameters of the study are:<br /><br>- measurement accuracy of energy expenditure<br /><br>- measurement accuracy of resting heart rate </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>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, interburst interval and VO2max estimation yes/no<br /><br>Additionally the wear comfort of the device will be evaluated with a<br /><br>questionnaire. </p><br>