REmote MOniToring usE in Suspected Cases of COVID-19 (Coronavirus): REMOTE-COVID Trial
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Coronavirus
- Sponsor
- Imperial College London
- Enrollment
- 15
- Locations
- 1
- Primary Endpoint
- Deterioration Resulting in Healthcare Review
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
The study aims to see if participant deterioration due to suspected coronavirus in a designated location (e.g. hotel) can be identified sooner by wearing the sensor. If sick patients can be identified early, participants are more likely to have better outcomes; the study believes that the sensor can help us do this. The sensor measures heart rate, respiratory rate and temperature every 2 minutes and this can be reviewed by the clinical team looking after the participants.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Aged 18 years or over.
- •Able to provide written consent.
Exclusion Criteria
- •Any participants that withdraw their consent.
- •A skin condition/reaction preventing wearing the wearable sensor.
- •The presence of a permanent pacemaker or cardiac defibrillator.
- •Any form of psychiatric disorder or a condition that, in the opinion of the investigator, may hinder communication with the research team.
- •Inability to cooperate or communicate with the research team.
Outcomes
Primary Outcomes
Deterioration Resulting in Healthcare Review
Time Frame: 1 year
Detection of clinical deterioration using wearable sensors resulting in healthcare review (e.g. GP telephone consultation)
Secondary Outcomes
- Hospitalisation(1 year)