Post-Intensive Care Risk-adjusted Alerting and Monitoring (PICRAM Phase 2)
Not Applicable
Completed
- Conditions
- Critical careNot Applicable
- Registration Number
- ISRCTN32008295
- Lead Sponsor
- niversity of Oxford (UK)
- Brief Summary
2024 Results article in https://pubmed.ncbi.nlm.nih.gov/38609314/ (added 15/04/2024)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 500
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
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
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To collect a large dataset containing physiological data on patients
- Secondary Outcome Measures
Name Time Method To demonstrate the feasibility of using commercially available