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DeliriumNCT06999967

Stanford-Lucidify EEG Delirium Study

An observational study of Delirium and Cognitive Dysfunction, run by Stanford University at 1 site in United States.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 55 years and older
Conditions the study is for
Delirium, Cognitive Dysfunction
What is being tested?
Electroencephalogram (EEG)
How many people
80 participants
Where
1 siteUnited States
Study dates
1 Jun 2025to 30 May 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 55 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Subjects admitted to the ICU or Oncology hospital wards

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Derek O Pipolo, M.D. contact

949-945-4992

dpipolo@stanford.edu

Dina Ganji, M.D. contact

925-558-6733

dganji@stanford.edu

United States1 site
  • Stanford Hospital and Clinics

    Stanford, California, 94305

    Derek O Pipolo, M.D., 949-945-4992, dpipolo@stanford.edu

    Dina Ganji, M.D., 925-558-6733, dganji@stanford.edu

Other trials in United States

About this study

Official title: Stanford-Lucidify Delirium Monitoring Pilot Study

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.

Read the detailed description

Study investigators would like to use a portable electroencephalogram (pEEG), the CGX EEG system (a Research-grade 2-Channel EEG device) to measure the brainwaves of patients admitted to Stanford Medical Center. Study investigators will then use the Lucidify software to allow for the interpretation of obtained brainwaves in order to detect delirium as early as possible, in order to minimize the detrimental effects of delirium in cognition and behavior. The Lucidify algorithm, different from our previously utilized EEG system (see below for details) can provide two additional features not previously available: (1) accelerometer data (an indicator of the level of patient's movements and a proxy for delirium phenotype; and (2) scored polysomnography data (providing validated interpretation of the patient's spectral sleep - thus a true measure of the patient's various stages and quality of sleep; which has direct implications on both the progression of delirium and the patient's overall health and recovery). Finally, the CGX system is simpler, more comfortable to wear, and better tolerated by medically ill patients.

The primary objective is to monitor the development and progression of delirium (acute confusion) and sleep disturbances associated with medical illness over time. The study will focus on two distinct patient populations: 1) patients admitted to an adult intensive care unit (ICU), and 2) patients in oncology units with hematologic malignancies undergoing cellular therapies or hematopoietic stem cell transplants (e.g., stem cell and Chimeric Antigen Receptor T-cell (CAR-T) Therapy). The rationale for targeting the occurrence of delirium, as its development has been associated with significantly poor hospital care outcomes and increased morbidity (medical complications) and mortality (death). The two patient populations have been specifically selected for the following reasons: Delirium is frequently observed in the ICU setting, with a reported prevalence of up to 85%. In the hematologic malignancies undergoing cellular therapies or hematopoietic stem cell transplants population, there is a significant prevalence of neurotoxicity associated with delirium, ranging from 20% to 60%. This neurotoxicity can lead to comorbid risks such as seizures and cerebral edema, and it is also associated with long-term cognitive impairment and depression (Hayden 2022, Ruark 2020).

In comparison to other portable EEG devices, the CGX EEG system investigators intend to investigate during the course of this specific study is more user-friendly (i.e., smaller, more portable, and has no wirings attaching the patient to the bed or an external device) , allowing for continuous monitoring without patient discomfort or interference associated with other monitoring systems currently used in our ICU setting. In addition to this system's tolerability and simplicity, this new device and AI-algorithm allows for the acquisition of two significant variables not previously available: (a) its algorithm allows for accelerometer data acquisition (this is a measure of the patient's motion, which will constitute an ideal and objective measure of the delirium phenotype (e.g., hypoactive, hyperactive, or mixed delirium subtype); and (b) the system allows for the measurement of the various phases of the sleep cycle, thus providing a full hypnogram of the quality and duration of sleep. Taking advantage of the enhanced comfort of wearing this new system; given the waxing and waning nature of delirium (i.e., how quickly it can vary through the course of 24-hrs) and In order to take full advantage of the system's capabilities, study investigators need the CGX recorder to remain in place 24/7 for the duration of the study.

Being tested
Electroencephalogram (EEG)
Keywords
Delirium, EEG, Encephalopathy, Cognitive Dysfunction, Electroencephalography, Delirium Monitoring
Medical subject headings
Delirium, Cognitive Dysfunction, Brain Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Electroencephalogram (EEG)Diagnostic test

    All study subjects will undergo monitoring via a portable electroencephalogram (pEEG), the CGX EEG system (a Research-grade 2-Channel EEG device) to measure the brainwaves of patients admitted to Stanford Medical Center. Investigators will then use the Lucidify software to allow for the interpretation of obtained brainwaves for the detection of delirium .

Study groups in NCT06999967
Study groupRoleWhat they receive
ICU PopulationSubjects admitted to the Intensive Care Unit (ICU)
Receives: Diagnostic Test: Electroencephalogram (EEG)
Oncology PopulationSubjects admitted to oncology units with hematologic malignancies undergoing cellular therapies or hematopoietic stem cell transplants (e.g., stem cell and Chimeric Antigen Receptor T-cell (CAR-T) Therapy)
Receives: Diagnostic Test: Electroencephalogram (EEG)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of subjects with delirium accurately diagnosed by the CGX EEG/Lucidify System

    Record and collect EEG brain waves on study subjects using the CGX EEG/Lucidify System to assess EEG features to differentiate between delirium positive and delirium negative patients.

    Measured: 24-hours a day monitoring for a minimum of 3 days from enrollment to the end of the study period (maximum of 7 days post-enrollment)

  2. Development of Delirium

    Number of subjects diagnosed with delirium

    Measured: From enrollment to the end of the study period (maximum of 7 days post-enrollment)

  3. Determination of Delirium Phenotype

    For those who develop delirium, the phenotype of delirium will be determined as per the Liptzin-Levkoff Criteria (based on DSM diagnostic Criteria). As such, all delirium episodes will be categorized as: hyperactive, hypoactive, mixed, or subsyndromal delirium. In addition, this phenotype determination will be compared with the CGX/Lucidify EEG System accelerometer data to determine concordance between the two.

    Measured: From enrollment to the end of the study period (maximum of 7 days post-enrollment)

Secondary outcomes (10)
  1. Immediate Post-hospital Admission Mortality

    Mortality following admission to the ICU or oncology wards

    Measured: From date of admission up to time of discharge (assessed up to 1 year after admission)

  2. Length of ICU & Hospital Stay

    Total number of days admitted to the hospital

    Measured: From date of admission up to time of discharge of the ICU or oncology ward, and then from the hospital (assessed up to 1 year after admission)

  3. Polysomnography Sleep Metrics - Stages of Sleep

    Assessment of the quality of the various sleep stages.

    Measured: 24 hours a day for a maximum of 7 days

  4. Polysomnography Sleep Metrics - Depth of sleep

    Assessment of the quality of the depth of sleep.

    Measured: 24 hours a day for a maximum of 7 days

  5. Polysomnography Sleep Metrics - Duration of Sleep

    Assessment of the duration of sleep.

    Measured: 24 hours a day for a maximum of 7 days

  6. Accelerometry Metrics - Acceleration Magnitude

    Assessment of the overall acceleration experienced by the device, useful for assessing movement intensity to measure the amount and degree of patient motion as a proxy for delirium motoric phenotype.

    Measured: 24 hours a day for a maximum of 7 days

  7. Accelerometry Metrics - Activity Counts

    Assessment of the number of subject movement events detected.

    Measured: 24 hours a day for a maximum of 7 days

  8. Accelerometry Metrics - Frequency of Movement

    Assessment of the rate at which movements occur, which can indicate activity patterns specific to a delirium motoric phenotype.

    Measured: 24 hours a day for a maximum of 7 days

  9. Accelerometry Metrics - Duration of Activity

    Assessment of the total time spent in different activity states, which can be indicative of a specific delirium motoric phenotype.

    Measured: 24 hours a day for a maximum of 7 days

  10. Accelerometry Metrics - Movement Variability

    Assessment of the variability in movement patterns, which can be indicative of a delirium motoric phenotype.

    Measured: 24 hours a day for a maximum of 7 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted31 May 2025
  2. Study start1 Jun 2025 (estimated)
  3. Primary completion30 Sep 2025 (estimated)
  4. Study completion30 May 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06999967
Sponsor's protocol ID
81015
Status last verified
May 2025
First submitted
16 May 2025
Last updated
31 May 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Delirium and Cognitive Dysfunction, run by Stanford University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 31 May 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Derek O Pipolo, M.D. (949-945-4992, dpipolo@stanford.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of subjects with delirium accurately diagnosed by the CGX EEG/Lucidify System (time frame: 24-hours a day monitoring for a minimum of 3 days from enrollment to the end of the study period (maximum of 7 days post-enrollment)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 May 2025.

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