Remote Monitoring Use In Cases Of Suspected COVID-19 (Coronavirus)
Completed
- Conditions
- Coronavirus
- Registration Number
- NCT04337489
- Lead Sponsor
- Imperial College London
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 15
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.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Deterioration Resulting in Healthcare Review 1 year Detection of clinical deterioration using wearable sensors resulting in healthcare review (e.g. GP telephone consultation)
- Secondary Outcome Measures
Name Time Method Hospitalisation 1 year Deterioration resulting in hospitalisation
Trial Locations
- Locations (1)
Imperial College London
🇬🇧London, United Kingdom