Non-invasive wireless continuous monitoring of vital signs using wearable sensors: a clinical validation study

Non-invasive wireless continuous monitoring of vital signs using wearable sensors: a clinical validation study - Vital signs monitoring with wearable sensors

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON45752

Enrollment

100

Registered

2016-07-20

Start date

2017-02-20

Completion date

Unknown

Last updated

2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Apneu, tachypneu apnea hypoventilation

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Age > 18 years Patients at risk for developing complications at the surgical ward

Exclusion criteria

Exclusion criteria: Known skin allergy Implanted medical devices, such as a cardioverter defibrillator or a pacemaker

Design outcomes

Primary

Measure	Time frame
Primary outcome is the accuracy of respiratory rate and heart rate during ward admission as derived with the wearable patch sensors (HealthPatch and SensiumVitals) and the contactless EarlySense system and compared with the reference standard.	—

Secondary

Measure	Time frame
Secondary outcome is the time delay of detecting critical adverse events such as respiratory arrest, severe bradypnea, cardiac arrest or severe bradycardia compared with the reference standard.	—

Countries

Netherlands

Outcome results