Could daylight hold the key to preventing delirium?
NCT ID NCT07791472
First seen Aug 28, 2026 · Last updated Aug 28, 2026
Summary
This pilot study investigates whether changes in the body clock, influenced by light exposure, are linked to delirium in critical care patients. Researchers will measure light levels at the bedside, collect blood samples to check for body clock markers and proteins related to delirium, and assess participants for confusion. After leaving critical care, participants will take memory and thinking tests. The goal is to understand why lack of daylight is a risk factor for delirium and to identify potential treatment targets.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Light exposure management and blood biomarker analysis
- What this could lead to
- If this pilot succeeds, it could point toward new ways to prevent delirium and reduce memory and thinking problems after critical illness.
- What could go wrong
- This is a small pilot study with only 10 participants, so findings may not apply broadly. It aims to test feasibility, not to prove that light interventions work.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 10 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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May 2027
An estimate. End dates often move.
- 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
Adult patients in critical care
- Ages
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50 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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 \>50 years old * Patients admitted to critical care in previous 24 hours * Patients with an arterial or venous access line suitable for blood sampling * Patients with an expected length of stay \>36 hours Exclusion Criteria: * Patients with a primary neurosurgical diagnosis * Patients with pre-existing cognitive impairment * Patients expected to die within 24 hours or receiving end of life treatment
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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King's College Hospital NHS Foundation Trust
RECRUITINGLondon, United Kingdom
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