eDIS-ICU: An international validation study to improve accuracy of screening for delirium in the ICU - A sub-analysis using ICDSC data from two institutions in Japa
Not Applicable
- Conditions
- delirium
- Registration Number
- JPRN-UMIN000047064
- Lead Sponsor
- KAWASAKI MEDICAL SCHOOL HOSPITAL Department of Nursing
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 220
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with severe cognitive impairment that interferes with their ability to understand and answer questions. Patients who do not understand Japanese and are unable to comprehend the research consent process or evaluation instructions. Patients who have visual or hearing impairment and cannot hear verbal evaluation instructions or see the application screen.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method - Sensitivity of the eDIS-ICU compared to the ICDSC to the DSM-V (gold standard).
- Secondary Outcome Measures
Name Time Method Prevalence of delirium during the observation period. concordance of delirium prevalence between eDIS-ICU, CAM-ICU and DSM-V. Reliability is defined as a Kappa coefficient greater than or equal to 0.6. Other measures of diagnostic accuracy (specificity, PPV, NPV, diagnostic odds). time taken (in seconds) to administer the eDIS-ICU and CAM-ICU. number of occasions in which the eDIS-ICU could be completed compared to the CAM-ICU.