The Application of a Wireless Sensor Technology for Vital Statistics in CHILDREN AND ADULTS

NAUnknownINTERVENTIONAL
Enrollment

500

Participants

Timeline

Start Date

December 31, 2021

Primary Completion Date

September 30, 2023

Study Completion Date

December 31, 2023

Conditions
FeverCOPDObesityCongenital Heart DiseaseRespiratory Distress
Interventions
DEVICE

Cardiorespiratory monitor

Subjects will also be fitted with conventional monitoring devices as per the standard of care (3 or 5 lead ECG, pulse oximeter, blood pressure cuff) and will have vital statistics obtained by a trained research assistant at regular 5-minute intervals including blood pressure, heart rate, temperature, and respiratory rate using the standard cardiorespiratory bedside monitor's cycling protocol. The same parameters will be obtained from the wireless sensor at identical time points for a duration of 2 hours. Data obtained from both conventional and study sources will be entered into an encrypted USB device for later analysis.

DEVICE

Wireless pressure sensor

Following informed consent, each subject will be fitted with a wireless sensor attached to a conventional laptop computer. The sensors fit around the participant's chest and work as transducers.

Trial Locations (1)

N6A2V5

Children's Hospital London Health Sciences Center, London

Sponsors
All Listed Sponsors
collaborator

Lauren Faught

UNKNOWN

collaborator

Michael Greff

UNKNOWN

collaborator

Michael Rieder

UNKNOWN

collaborator

Safieddin Safavi-Naeini

UNKNOWN

lead

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

OTHER

NCT01845506 - The Application of a Wireless Sensor Technology for Vital Statistics in CHILDREN AND ADULTS | Biotech Hunter | Biotech Hunter