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Automated spot-check respiration and pulse monitoring for 5-18 year old patients

Completed
Conditions
vital signals monitoring
monitoring
signals
Registration Number
NL-OMON40772
Lead Sponsor
Philips Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

Patients of MMC- pediatric department
-Age between 5 and 18 years old
-Subjects must be able to provide an informed consent or have legally authorized representative consent to participate
-Subjects of 12 years and older must provide assent to participate
-Subjects are hospitalized patients of the pediatric department of MMC and stay there for at least 24 hours.

Exclusion Criteria

Exclusion criteria for subject selection
* Subjects with deformations that prevent proper device positioning
* Subjects with arrhythmia
* Subjects who had rib surgery
* Subjects with skin irritation that prevent 24 hours wearing the device
* Subjects having implants or devices connected that might be affected by the bioimpedance measurement.

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Primary objective:<br /><br>The primary objective is obtaining motion sensor data for performance<br /><br>validation of a respiration rate and pulse rate monitoring algorithm for use on<br /><br>5-18 years old patients.<br /><br>The data collected using the motion sensor of this study will be compared with<br /><br>the one obtained using the golden standard for respiratory frequency ( by<br /><br>using a respiration band) and heart rate (by using ECG) .</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>The secondary objective is obtaining motion sensor data for the development and<br /><br>improvement of respiration rate and pulse rate detection algorithms specific<br /><br>for 5-18 years old patients.</p><br>
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