A comparative study of the effectiveness of routine care and ABCDEF bundle implementation based on appreciative leadership theory
Not Applicable
- Conditions
- Intensive Care.
- Registration Number
- IRCT20221019056240N1
- Lead Sponsor
- Bagheiat-allah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Obtaining informed consent from the patient or family
Hospitalization for more than 72 hours in the intensive care unit
Patients with internal diseases
18 years and older patients
Non-psychotic patients
Non-pregnant Patients
Patients who do not have severe dementia
Lack of major damage to the nervous system leads to severe cognitive and motor deficits
Exclusion Criteria
Dying patients
Patients having active seizures
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity. Timepoint: three times a day and at 8, 16 and 24 hours and for 3 days. Method of measurement: using a visual analogue scale.;Delirium. Timepoint: three times a day and at 8, 16 and 24 hours and for 3 days. Method of measurement: Using the Persian version of the CAM-ICU tool.;Weaning from mechanical ventilation. Timepoint: Daily. Method of measurement: Record the hours of successful weaning from mechanical ventilation or reintubation (unsuccessful weaning).
- Secondary Outcome Measures
Name Time Method Mortality Rate. Timepoint: At the end of the study. Method of measurement: Census of patients of both groups.;ICU length of stay. Timepoint: At the end of the study. Method of measurement: Counting the days of patients staying in the intensive care unit.