DeliriumNCT06999967
Stanford-Lucidify EEG Delirium Study
An observational study of Delirium and Cognitive Dysfunction, run by Stanford University at 1 site in United States.
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.
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
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.
- Conditions
- Delirium, Cognitive Dysfunction
- 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 group | Role | What they receive |
|---|---|---|
| ICU Population | Subjects admitted to the Intensive Care Unit (ICU) Receives: Diagnostic Test: Electroencephalogram (EEG) | |
| Oncology Population | Subjects 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.
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)
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)
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)
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)
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)
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
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
Polysomnography Sleep Metrics - Duration of Sleep
Assessment of the duration of sleep.
Measured: 24 hours a day for a maximum of 7 days
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
Accelerometry Metrics - Activity Counts
Assessment of the number of subject movement events detected.
Measured: 24 hours a day for a maximum of 7 days
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
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
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.
- First posted31 May 2025
- Study start1 Jun 2025 (estimated)
- Primary completion30 Sep 2025 (estimated)
- Study completion30 May 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for DeliriumStudies of the same condition, open and under way.
- More trials run by Stanford UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Stanford University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Jose R Maldonado, MD, Stanford University
- Investigators
- José R Maldonado, M.D., Principal investigator, Stanford University
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
Study at a glance
From the registry record, last updated by the sponsor on 31 May 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Stanford-Lucidify Delirium Monitoring Pilot Study
- ClinicalTrials.gov ID
- NCT06999967
- Acronym / sponsor ID
- 81015
- Conditions
- Delirium, Cognitive Dysfunction
- Keywords
- Delirium, EEG, Encephalopathy, Cognitive Dysfunction, Electroencephalography, Delirium Monitoring
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 80 participants (estimated)
- Lead sponsor
- Stanford UniversityUniversity, hospital or other
- Study start
- 1 Jun 2025 (estimated)
- Primary completion
- 30 Sep 2025 (estimated)
- Study completion
- 30 May 2026 (estimated)
- First posted
- 31 May 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| ICU Population | – | Diagnostic Test: Electroencephalogram (EEG)Subjects admitted to the Intensive Care Unit (ICU) |
| Oncology Population | – | Diagnostic Test: Electroencephalogram (EEG)Subjects 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) |
Who may qualify
- Ages
- 55 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Subjects admitted to the ICU or Oncology hospital wards
Key inclusion criteria (5 listed)
- 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
Key exclusion criteria (5 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Electroencephalogram (EEG)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 . | Diagnostic test | ICU Population, Oncology Population |
Primary outcome
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)
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.
Development of Delirium
Time frame: From enrollment to the end of the study period (maximum of 7 days post-enrollment)
Number of subjects diagnosed with delirium
Determination of Delirium Phenotype
Time frame: From enrollment to the end of the study period (maximum of 7 days post-enrollment)
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.
10 secondary outcomes
Immediate Post-hospital Admission Mortality
Time frame: From date of admission up to time of discharge (assessed up to 1 year after admission)
Length of ICU & Hospital Stay
Time frame: 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)
Polysomnography Sleep Metrics - Stages of Sleep
Time frame: 24 hours a day for a maximum of 7 days
Polysomnography Sleep Metrics - Depth of sleep
Time frame: 24 hours a day for a maximum of 7 days
Polysomnography Sleep Metrics - Duration of Sleep
Time frame: 24 hours a day for a maximum of 7 days
Accelerometry Metrics - Acceleration Magnitude
Time frame: 24 hours a day for a maximum of 7 days
Accelerometry Metrics - Activity Counts
Time frame: 24 hours a day for a maximum of 7 days
Accelerometry Metrics - Frequency of Movement
Time frame: 24 hours a day for a maximum of 7 days
Accelerometry Metrics - Duration of Activity
Time frame: 24 hours a day for a maximum of 7 days
Accelerometry Metrics - Movement Variability
Time frame: 24 hours a day for a maximum of 7 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 May 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
José R Maldonado, M.D. principal investigator
Stanford University
1 site in 1 country: see every site and its status.
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.