Post-intensive care syndrome prevalence and associated factors in surgical critical care survivors
- Conditions
- Symptoms, signs and abnormal clinical and laboratory findings, NEC
- Registration Number
- KCT0008984
- Lead Sponsor
- Asan Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Selection criteria:
a. Individuals who have been admitted to the surgical ICU for more than 72 hours and subsequently transferred to general wards.
b. Adults aged 18 years or older.
c. Individuals without neurological disorders such as brain injury or stroke.
d. Individuals with no hearing or visual impairments, enabling effective communication.
e. Individuals who understand the purpose and methods of the study and voluntarily agree to participate.
a. Patients who have consented to the withdrawal of life-sustaining treatment and have been transferred to general wards.
b. Patients who are unable to engage in verbal communication.
c. Individuals who are homeless, living alone, or are expected to have difficulties with future outpatient visits, etc.
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method After one week from discharge from the intensive care unit, the patient's physical function will be assessed.;After one week from discharge from the intensive care unit, the patient's cognitive function will be assessed.;After one week from discharge from the intensive care unit, the cognitive function will be evaluated
- Secondary Outcome Measures
Name Time Method We are examining whether therapeutic characteristics influence the occurrence of post-intensive care syndrome;We are examining whether therapeutic characteristics influence the occurrence of post-intensive care syndrome