eDIS-ICU - An international validation study to assess accuracy of a new screening tool for delirium in the intensive care unit
Not Applicable
Recruiting
- Conditions
- DeliriumMental Health - Other mental health disorders
- Registration Number
- ACTRN12622000220763
- Lead Sponsor
- Metro North Hospital and Health Service
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 700
Inclusion Criteria
•Anticipated ICU length of stay of >24 hours from time of enrolment.
•Greater than or equal to 18 years.
•Able to communicate ‘Yes’ and ‘No’ consistently (verbal or non-verbal).
•Informed consent obtained by participant / their legal representative.
Exclusion Criteria
•Pre-existing severe cognitive impairment preventing them from comprehending / answering assessment questions (as determined by the treating clinical team in consultation with the research team).
•Insufficiently fluent in the language in use at the participating hospital to complete consent processes and/or follow instructions.
•Patients with visual / hearing impairment preventing them from hearing verbal assessment instructions or visualising the app screen.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sensitivity of eDIS-ICU compared to CAM-ICU.[Twice within 24 hours (morning and afternoon) immediately following enrolment.]
- Secondary Outcome Measures
Name Time Method