Multicomponent intervention program for preventing delirium for elderly ICU patients
- Conditions
- Not Applicable
- Registration Number
- KCT0004651
- Lead Sponsor
- Jeju National University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 52
The inclusion criteria were individuals without delirium at initial assessment, with expected ICU LOS of at least 48 hours, without communication difficulties, and with an informed consent of study participation signed by the patient him/herself or the guardian.
The exclusion criteria included a score of -4 or less in the Richmond Agitation and Sedation Scale (RASS), dementia, any psychiatric or neurological diagnosis, any primary brain lesions of the vascular, traumatic, malignant or infectious type, a period of continuous intravenous sedation, and absence of a guardian.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Delirium incidence
- Secondary Outcome Measures
Name Time Method Self-extubation or self-removal of catheter;Risk of fall;Length of stay