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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04927078
Other study ID # 287454
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 1, 2020
Est. completion date October 31, 2020

Study information

Verified date June 2021
Source Oxehealth Limited
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This project will use data obtained from a proprietary vision-based patient monitoring and management system (OxeVision) for measuring heart rate and respiratory rate which is in clinical use at the Coventry and Warwickshire Partnership NHS Trust.


Description:

The investigators will analyse data from patients with known COVID 19 infection both during, and where possible before clinical COVID 19 infection and controls to determine whether changes can be detected in these parameters that precede overt clinical deterioration. The role of remote vision-based patient monitoring and management in supporting the care of patients with COVID-19 will be assessed through staff interviews.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date October 31, 2020
Est. primary completion date October 31, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients age 18 and above. Patients on wards with a medical diagnosis of COVID 19 who are in rooms with the Vision based patient monitoring and management system. Exclusion Criteria: Children will be excluded. No data will be excluded unless specifically requested by the treating clinician.

Study Design


Intervention

Other:
Observation of breathing pattern
Observations will be collected using a remote vision based patient monitoring and management system.

Locations

Country Name City State
United Kingdom Coventry and Warwickshire Partnership NHS Coventry

Sponsors (2)

Lead Sponsor Collaborator
Oxehealth Limited Royal Brompton & Harefield NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Breathing rates Breathing rates collected via remote monitoring of participants using the Vision Based Patient Monitoring and Management System. Data will be collected throughout study completion, an average of 7 months, to obtain breathing rate before and after the diagnosis of COVID 19.
Secondary Pulse rates Pulse rate collected via remote monitoring of participants using the Vision Based Patient Monitoring and Management System. Data will be collected throughout study completion, an average of 7 months, to obtain pulse rate before and after the diagnosis of COVID 19.
Secondary BR and PR Similar data to be collected from control subjects Data will be collected throughout study completion, an average of 7 months, to obtain breathing and pulse rate before and after the diagnosis of COVID 19.
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