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Validation of Vital Signs Recording With VT-Patch Connected Devices in Children

Children | Oxygen Saturation | Intensive Care Unit | Vital Signs | Respiratory Rate | Heart Rate

: Patient readmission to PICU is a major point of concern for physicians because, although being a rare event, it has been strongly associated with more morbidity and death. Patient monitoring once they have left the PICU is drastically modified, and small connected devices could be an option to early identify patients at risk of PICU readmission. Such devices have been manufactured for the recording of vital signs in adults, but they do not exist for children.

Besides, studies have recently shown that devices that use optical sensors may be less accurate in individuals with dark skin pigmentation since dark skin tones impose a limitation on optical biometric sensing. The wearable and medical device industry has not sufficiently addressed this issue yet. This is one of the main challenges that need to be addressed in this area to make sure the connected devices using this technology will work with all different skin colours including very dark skin.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    1 to 18

Participation Criteria

Inclusion Criteria:

* PICU monitoring for the next 24 hours

Exclusion Criteria:

* Recent cardiac or thoracic surgery
* Thoracic skin lesion that contraindicates the VT patch
* No parental consent
* Intermittent presence of one study observer in the patient room considered inappropriate by the physician or the nurse in charge because of the child's medical condition

Study Location

VitalTracer Ltd
VitalTracer Ltd
Côte Saint-Luc, Quebec
Canada

Contact Study Team

Primary Contact

Azadeh Dastmalchi, PhD

[email protected]
(613) 276-1413
CHU Sainte Justin Hospital
CHU Sainte Justin Hospital
Montreal, Quebec
Canada

Contact Study Team

Primary Contact

Philippe Jouvet, MD, PhD

[email protected]
(514) 345-4931
Backup Contact

Azadeh Dastmalchi, PhD

[email protected]
(613) 276-1413
Study Sponsored By
VitalTracer Ltd.
Participants Required
More Information
Study ID: NCT05451875