Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Biosensor
  • COVID-19
  • Respiratory Failure
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Younger than 125 years
Gender
Both males and females

Description

Altair medical has developed a pre-commercial investigational wearable (chest-worn) biosensor which can measure continuous respiratory rate and respiratory events. This sensor has been verified to have good correlation with reference impedance plethysmography data. Inclusion criteria: All inpatients...

Altair medical has developed a pre-commercial investigational wearable (chest-worn) biosensor which can measure continuous respiratory rate and respiratory events. This sensor has been verified to have good correlation with reference impedance plethysmography data. Inclusion criteria: All inpatients in the QEUH with respiratory failure from any cause. Exclusion criteria: Lack of capacity to consent Physiology data will be correlated with event time-course data including oxygen and breathing support requirements, deterioration, hospital discharge and status at 28 days and 90 days post discharge. A small subset of patients will have further investigations - parasternal EMG; thoracic electrical impedance tomography; forced oscillometry and post discharge Altair and Fitbit data. Study analysis will include machine learning model development with the objective of developing risk-predictions for clinically significant deteriorations.

Tracking Information

NCT #
NCT04668313
Collaborators
  • Altair Medical
  • Storm ID
Investigators
Not Provided