The effect of multifactorial intervention on prevention of delirium in ICU patients of hospital
Not Applicable
Recruiting
- Conditions
- Delirium.Delirium due to known physiological condition
- Registration Number
- IRCT20201129049530N1
- Lead Sponsor
- Zahedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
age>18
Absence of delirium at the beginning of the study
less than 24 hours from hospitalization
Absence of Cognitive impairment
Absence of severe hearing and vision impairment
Organ health in the soles of the feet
Having the consent or knowledge to participate in the study (patient or first-degree companion)
GCS>9
Exclusion Criteria
Discharge, death or transfer earlier than 48 hours
The unwillingness of the patient or the patient's companion to continue participating in the study
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Delirium incidence. Timepoint: twice a day, from enterance of patients to the study upto 7 days. Method of measurement: RASS(Richmond Agitation Sedation Scale), CAM-ICU(Confusion Assessment Method for ICU), ICDSC(Intensive Care Delirium Screening Checklist).
- Secondary Outcome Measures
Name Time Method