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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04420182
Other study ID # CTO 3210
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 17, 2020
Est. completion date February 4, 2022

Study information

Verified date April 2022
Source Lawson Health Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This multicentre prospective cohort trial is designed to demonstrate effectiveness and efficiency of a virtual care model for the management of COVID-19 patients isolating at home. The investigators have reoriented existing technology and networks for this research project. The investigators are amplifying our existing virtual care platform VIRTUES, combining it with home monitoring of COVID-19 patients, to provide real-time evidence, harmonize data collection, and share data provincially to mitigate the impact of the rapid spread of the virus. The study will facilitate early detection of complications associated with the disease, treatment and management of COVID-19 patients at home. The research will be conducted provincially in Ontario. This initiative will provide evidence to inform clinical and health system management and public health response to COVID-19 patients isolating at home.


Recruitment information / eligibility

Status Completed
Enrollment 817
Est. completion date February 4, 2022
Est. primary completion date February 4, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All COVID-19 positive patients of age 18 or above - Participant must communicate in English or French language - An email address and account Exclusion Criteria: - Unable or unwilling to provide informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Virtual Care at Home
Participants will have access to the VIRTUES platform for COVID-19 Virtual Care at Home

Locations

Country Name City State
Canada St. Mary's General Hospital Kitchener Ontario
Canada London Health Sciences Centre London Ontario
Canada Ottawa Heart Research Institute Ottawa Ontario
Canada Niagara Health St. Catharines Ontario
Canada St. Joseph's Health Centre Toronto Ontario

Sponsors (2)

Lead Sponsor Collaborator
Lawson Health Research Institute Cardiac Arrhythmia Network of Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary 14 Day Patient Satisfaction Questionnaire The primary outcome measure is patient satisfaction as measured from a patient satisfaction questionnaire at 14 days. 14 days
Secondary Emergency Department Visits The secondary outcome measures will include the number of patients that require an Emergency Department visits during the observation period of 14 days. 14 days
Secondary 14 Day EQ-5D-5L Scores The secondary outcome measures will include the health status measures of the EuroQuality of Life Five Dimensions (EQ-5D-5L) at 14 days. Scoring is Level 1 to 5 for each dimension; higher scores meaning worse health status. 14 days
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