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Clinical Trials/NCT04337489
NCT04337489
Completed
Not Applicable

REmote MOniToring usE in Suspected Cases of COVID-19 (Coronavirus): REMOTE-COVID Trial

Imperial College London1 site in 1 country15 target enrollmentJuly 28, 2020
ConditionsCoronavirus

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.

Registry
clinicaltrials.gov
Start Date
July 28, 2020
End Date
March 26, 2021
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

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)

Study Sites (1)

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