Critical care Not Applicable
Conditions
Interventions
Before patients leave the intensive care unit, or shortly after they arrival on their new ward, the study monitoring equipment will be attached to them. This involves attaching some sticky dots to th
Sponsors
University of Oxford (UK)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Participant is willing and able to give informed consent for participation in the study 2. Aged 16 years or above 3. Discharged from adult intensive care unit. 4. Male and female participants
Exclusion criteria
Exclusion criteria: 1. Patients discharged for palliative care 2. Patients whose anatomy, condition or prior surgery precludes the use of the wearable monitoring equipment 3. Patients who cannot understand written English and for whom no translator can be found 4. Patients not able to give informed consent due to diminished capacity
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To collect a large dataset containing physiological data on patients | — |
Secondary
| Measure | Time frame |
|---|---|
| To demonstrate the feasibility of using commercially available | — |
Countries
England, United Kingdom
Outcome results
None listed