Stanford-Lucidify EEG Delirium Study
Starting soon
Conditions studied: Delirium, Cognitive Dysfunction
In brief
The purpose of this study is to evaluate the effectiveness of the CGX/Lucidify EEG system in enabling physicians to detect delirium (confusion) in medically ill patients as early as possible in order to minimize the detrimental effects of delirium. The study will involve collecting EEG data through the CGX EEG system (a Research-grade 2-Channel EEG device) and applying the Lucidify EEG software algorithm to identify indicators and degree of delirium, obtain data regarding the amount and degree of patient's movement and activity throughout the day in order to detail delirium subtype, and obtain data regarding the quality of the sleep as it affects delirium severity and duration. By enhancing early detection, this research aims to improve patient outcomes and inform clinical decision-making.
Key facts
- Study ID
- NCT06999967
- Run by
- Stanford University
- People needed
- 80
- Starts
- 2025-06-01
- Expected to finish
- 2026-05-30
- Last updated by the study team
- 2025-05-31
Who can join
Age: 55 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age is 55 years or older
- Clinical suspicion of delirium or subject at risk for delirium
- Admitted to the Intensive Care Unit (ICU) or Oncology wards
- Expected hospital stay is greater than one (1) day
- Subject must be fluent in English
You may not qualify if…
- Age is younger than 55 years
- Subjects with a primary neurological or neurosurgical condition such as stroke, epilepsy, brain tumor, or witnessed seizures, Parkinson's disease, traumatic brain injury, or s/p craniectomy
- Active CNS substance abuse, intoxication, or withdrawal
- Unarousable or unresponsive subjects with RASS <-3
- Subject is blind, deaf, or unable to speak or understand English
Where it is running
- Stanford Hospital and Clinics — Stanford, California, United States
Full record on ClinicalTrials.gov
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