on-invasive wireless continuous monitoring of vital signs using wearable sensors: a clinical validation study
Completed
- Conditions
- 10024967Apneu, tachypneuapneahypoventilation10007521
- Registration Number
- NL-OMON45752
- Lead Sponsor
- Divisie Vitale Functies
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
Age > 18 years
Patients at risk for developing complications at the surgical ward
Exclusion Criteria
Known skin allergy
Implanted medical devices, such as a cardioverter defibrillator or a pacemaker
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Primary outcome is the accuracy of respiratory rate and heart rate during ward<br /><br>admission as derived with the wearable patch sensors (HealthPatch and<br /><br>SensiumVitals) and the contactless EarlySense system and compared with the<br /><br>reference standard. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary outcome is the time delay of detecting critical adverse events such<br /><br>as respiratory arrest, severe bradypnea, cardiac arrest or severe bradycardia<br /><br>compared with the reference standard.</p><br>