Activity and heart rate monitor heart rate algorithm validation study

Completed

• Conditions: sub-optimal physical fitness; 10003018; 10082206; Sedentary behavior

• Registration Number: NL-OMON42837
• 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: 11

Inclusion Criteria

-18 years of age or older
-Body Mass Index (BMI) between 19 and 35

Exclusion Criteria

- Suffer 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 the accuracy of energy expenditure and<br /><br>resting heart rate measurement of newly developed software in reference to<br /><br>currently approved software.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary parameter is to asses the measurement accuracy of newly developed<br /><br>software in reference to currently approved software over 10 second averaged<br /><br>values.</p><br>