Could a quieter, dimmer ICU protect Patients' brains?
NCT ID NCT06294158
First seen Sep 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time
Summary
Delirium is a common and serious problem for critically ill patients in intensive care units. Researchers at the Medical University of Graz are measuring light and noise levels in three ICUs to see whether these environmental factors are associated with the development of delirium. They will enroll about 250 to 300 adult patients who are expected to stay in the ICU for at least two more days, and they will assess each patient daily for delirium using a standard bedside test. The goal is to learn whether adjusting ICU lighting and sound could become a way to reduce delirium risk.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If light and noise levels are linked to delirium, hospitals could adjust ICU lighting and sound to help protect patients' thinking and memory during critical illness.
- What could go wrong
- This is an observational pilot study, so it can show associations but not prove that light or noise causes delirium. Many other factors affect delirium risk, and the findings may not apply to other hospitals or patient groups.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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315 people
The number who actually took part.
- Started
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Oct 2024
- Finished
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Apr 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients shall be included into the study if they can be expected to remain in the ICU for at least another two days, if they are not yet in delirium, if the ICU environment is not actively modified for therapeutic reasons (e.g., in the treatment of burns patients), if no treatment limitations are in place and if the patient can provide written informed consent. In those patients, who cannot provide informed consent upon recruitment due to their current illness or injury, consent by patients or their representatives shall be sought if and once they regain capacity (deferred consent).
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria * Adult patients (age ≥ 18 years) * Admission to participating Intensive Care Unit * Expected (further) stay in participating Intensive Care Unit ≥ 48 hours * Not (currently) deeply sedated (RASS ≥ -3) Exclusion Criteria * Patient already in delirium (CAM-ICU positive) * Environmental modification due to treatment necessities (e.g., burns care) * Advanced directives / Treatment limitation * Current inclusion in other (interventional) trial * Documented patient refusal in advance
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University Medical Centre Graz, Dept. of Anaesthesiology and Intensive Care Medicine
Graz, Styria, 8036, Austria
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