Actively Recruiting
Family Involvement in the Intensive Care Unit A Prospective Study on Effects on Sedation, Delirium, Ventilator Use, and Length of Stay
Led by Istanbul University - Cerrahpasa · Updated on 2025-01-17
122
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to explore how spending time with family members affects patients treated in a tertiary intensive care unit (ICU). It focuses on whether increased family involvement can reduce the need for sedative medications, lower the occurrence of delirium, decrease the number of days on a ventilator, and shorten the length of ICU stays. The study examines these patient outcomes in a real-world ICU setting. Participants are adult ICU patients who have at least one family member actively involved in their care during their ICU stay. The study observes these patients prospectively, monitoring how time spent with relatives may influence sedation needs and other clinical outcomes. No specific treatment interventions are given, as this is an observational cohort study. During the study, each patient's sedative dose is recorded daily for up to the first four weeks in the ICU. Researchers will also assess delirium, ventilator usage, and length of ICU stay. Participation involves monitoring these health measures and family involvement without changing standard care. The study includes adult patients aged 18 and older and continues throughout their ICU admission as long as they remain eligible.
CONDITIONS
Official Title
Family Involvement in ICU
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 and over.
- Patients with at least one family member actively involved in the care process in the ICU.
You will not qualify if you...
- Patients with pre-existing cognitive impairment or dementia.
- Patients with severe traumatic brain injury.
- Patients with an expected mortality in the ICU of more than 80%.
- Absence of family members for patients admitted to the ICU.
AI-Screening
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Trial Site Locations
Total: 1 location
1
Cerrahpaşa Medical Faculty
Istanbul, Turkey (Türkiye), 34153
Actively Recruiting
Research Team
O
Oguzhan Kayhan
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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