Actively Recruiting
Light and Noise: Studying Environmental Risk Factors for Delirium in Intensive Care Units
Led by Medical University of Graz · Updated on 2025-01-22
250
Participants Needed
1
Research Sites
56 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating how environmental factors in intensive care units (ICUs), such as noise and light levels, may influence the development of delirium in critically ill adults. Delirium is a serious medical condition involving confusion and cognitive disturbances that can affect patient outcomes and survival. This observational pilot study aims to identify potentially modifiable ICU environmental risks that could improve patient care and ICU design in the future. The study will be conducted at three perioperative ICUs at the University Medical Centre Graz over one year, enrolling 250 to 300 adult patients expected to stay at least two more days in the ICU. Patients who are not deeply sedated and not currently delirious will be included. Noise and ambient brightness levels will be measured repeatedly using sound level meters and lux meters throughout the day. Daily assessments for delirium will be performed using the Confusion Assessment Method for the ICU (CAM-ICU). Vital signs and treatment details will also be recorded daily. Participants will undergo baseline data collection relevant to delirium risk and overall ICU outcomes. Researchers will track environmental noise and light alongside physiological and clinical data to analyze associations with delirium occurrence. Statistical methods, including logistic regression, will be used to identify factors linked to delirium development over a seven-day period. This study does not involve administering treatments but focuses on monitoring and evaluating environmental and clinical parameters in ICU patients.
CONDITIONS
Official Title
Light and Noise: Objectively Assessing Environmental Risk Factors for Delirium in the ICU
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients aged 18 years or older
- Admission to a participating Intensive Care Unit
- Expected to remain in the Intensive Care Unit for at least 48 hours
- Not deeply sedated (Richmond Agitation-Sedation Scale score greater than or equal to -3)
You will not qualify if you...
- Patient currently diagnosed with delirium (CAM-ICU positive)
- ICU environment actively modified for treatment reasons (e.g., burns care)
- Advanced directives or treatment limitations in place
- Currently enrolled in another interventional clinical trial
- Patient has documented refusal to participate
AI-Screening
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Trial Site Locations
Total: 1 location
1
University Medical Centre Graz, Dept. of Anaesthesiology and Intensive Care Medicine
Graz, Styria, Austria, 8036
Actively Recruiting
Research Team
P
Paul Zajic, MD PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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