Behavioral Monitoring in ICUAIME-ICUNCT07307521
Exploring the Use of AI-Assisted Video Monitoring to Predict Accidental Events in ICU Patients
An observational study of Behavioral Monitoring in ICU and Prediction of Accidental Events Using AI-Assisted Video Analysis, run by Shanghai Zhongshan Hospital.
Trial summary
This study aims to improve the safety and care of patients in the Intensive Care Unit (ICU) by using artificial intelligence (AI) to analyze video monitoring. ICU patients often face serious risks such as delirium, accidental removal of breathing tubes or lines, and sleep problems. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Behavioral Monitoring in ICU, Prediction of Accidental Events Using AI-Assisted Video Analysis, ICU Patient Safety and Early Warning System
- What is being tested?
- AI-Assisted Video Monitoring
- How many people
- 300 participants
- Where
- No sites listed yet
- Study dates
- 1 Jan 2026to 31 Dec 2028
- How long will I take part?
- 7 Days
- 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 Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: The study population consists of ICU patients who undergo continuous bedside monitoring as part of routine critical care. Participants include adults and pediatric patients admitted to a mixed medical-surgical ICU. Individuals are enrolled only after informed consent is obtained from the patient or a legally authorized representative. The cohort represents typical ICU patients at risk for behavioral or accidental events such as agitation, delirium, sleep disturbance, or unplanned device removal. The population reflects real-world conditions and clinical diversity, allowing evaluation of AI-assisted video monitoring across a broad range of critical illness severity and diagnoses.
Who may be able to join
- Adult or pediatric patients admitted to the Intensive Care Unit (ICU).
- Patient or legally authorized representative is capable of understanding the study information and providing informed consent.
- Patient is expected to remain in the ICU long enough to allow video and physiologic data collection.
- Agreement to participate and allow video monitoring during the ICU stay.
Who cannot join
- Refusal to participate from the patient or legally authorized representative.
- Patients for whom continuous video monitoring is medically inappropriate or not feasible (e.g., isolation conditions preventing camera installation).
- Patients whose condition or legal status requires special restrictions on video recording (e.g., certain forensic or custodial cases).
- Any situation judged by the clinical team to place the patient at increased privacy or safety risk by participation.
- Withdrawal of consent at any point during the study.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
This study aims to improve the safety and care of patients in the Intensive Care Unit (ICU) by using artificial intelligence (AI) to analyze video monitoring. ICU patients often face serious risks such as delirium, accidental removal of breathing tubes or lines, and sleep problems. These events can lead to medical emergencies, longer ICU stays, higher costs, and worse outcomes.
To address these challenges, we will place a small video camera above each ICU bed. The camera will record patient movements, body activity, and sleep patterns. At the same time, routine medical monitors will record heart rate, blood oxygen levels, and other vital signs. Noise levels in the room will also be measured. All these data help us understand the patient's behavior and condition more accurately.
Read more
The video recording does not involve extra treatment or additional procedures. All data are collected passively and safely. Patient privacy is strictly protected: the system will blur faces or replace them with digital avatars, and any information that could identify the patient or the environment will be masked. All videos are stored securely inside the hospital and are processed only after privacy protection.
Using these recordings, an AI model will be trained to recognize early warning signs of dangerous situations. For example, the system may detect early movements that suggest the patient is becoming agitated, confused, or trying to remove medical tubes. It may also identify severe sleep disturbance that may lead to delirium. If the AI can recognize these early changes, medical staff can intervene sooner and prevent harm.
About 300 patients from Fudan University Zhongshan Hospital will participate. Participation is voluntary. Patients or families will sign an informed consent form before being enrolled. The study has three stages:
Screening - understanding the study and signing consent. Data collection - video and medical monitor data are collected during the ICU stay.
Follow-up - telephone or in-person follow-up at 1 month and 6 months after discharge to evaluate recovery, sleep, mental status, and overall safety.
There are no direct medical risks from participating in this study because it only collects behavioral and monitoring data. The cameras do not interfere with treatment. Privacy and data security are the main considerations, and all measures strictly follow national laws and hospital regulations.
Participants may benefit from earlier identification of dangerous situations, which may help prevent accidental tube removal, severe agitation, or other emergencies. Even if no direct benefit occurs, the information collected may help improve future ICU care by enabling safer and more accurate monitoring systems.
Taking part in the study will not affect the patient's medical care. Patients may withdraw at any time without any consequences or loss of benefits.
This study hopes to build a reliable AI tool that can assist nurses and doctors in recognizing early signs of trouble, improving safety, and enhancing the quality of care for ICU patients.
Read the detailed description
This study investigates whether artificial intelligence (AI)-assisted video monitoring can identify early behavioral changes that precede accidental or harmful events in Intensive Care Unit (ICU) patients. ICU patients are vulnerable to a series of sudden and potentially dangerous events-such as agitation, delirium, accidental device removal, and significant sleep disruption-many of which develop gradually and are difficult to detect solely from routine physiological monitoring. This project aims to determine whether AI analysis of continuous bedside video recordings, combined with noise-level information and vital-sign data already collected during standard ICU care, can provide clinicians with timely warnings before these events occur.
Rationale Traditional ICU monitoring systems focus on physiological parameters such as heart rate, blood pressure, and oxygen saturation. While essential, these measurements do not fully represent patient behavior. Many high-risk events are preceded by subtle motor patterns or behavioral cues-for example, repeated reaching toward tubes, rising restlessness, or disturbed sleep cycles. Such cues are often intermittent, brief, or masked by sedation or other treatments, making them difficult for staff to detect in busy clinical environments.
Computer vision and AI technologies offer an opportunity to objectively observe and interpret patient movements and behavioral trends continuously, without adding clinical workload. By integrating video information with physiologic data and environmental noise levels, the AI system may identify patterns that indicate emerging delirium, increased agitation, or imminent attempts to remove medical devices. Early identification may support timely preventive interventions and reduce the rates of adverse events.
Study Overview The study will prospectively enroll ICU patients who consent to video monitoring and data use. A small camera will be installed above each bed to continuously capture patient movement and posture. The camera view is restricted to the patient zone, excluding unnecessary areas such as the nursing station. All recordings follow strict privacy-protection procedures, including automated face masking, background blurring, and removal of identifying information from objects in the frame.
Environmental noise is recorded through a decibel meter, and routine vital-sign data are synchronized with the video timeline. These combined multimodal data will serve as input for AI model development.
The study is divided into three components:
Data collection phase - real-world continuous recording of behavioral and physiological data.
Data processing and annotation - cleaning, de-identification, and labeling of key behavioral events by trained researchers.
Model development and evaluation - training AI models to identify behavioral patterns associated with clinically meaningful events, and evaluating their predictive performance.
Data Integration and Processing
All raw videos remain stored securely inside the hospital's protected data environment and are not transferred outside. A standardized de-identification pipeline is applied before any analytical use. This includes:
Masking or replacing patient faces. Removing identifying elements such as bed numbers and equipment labels. Blurring all background areas outside the patient zone. Excluding frames containing staff faces or unrelated activities. After de-identification, videos are aligned with vital-sign and noise-level timelines to create multimodal time-series datasets. Human annotators, trained with a unified labeling guideline, identify episodes of agitation, possible delirium-related behavior, attempts at device removal, and sleep-wake transitions. These labels serve as ground truth for AI training.
AI Model Development Multiple AI architectures will be explored, particularly those suited for temporal video analysis. Potential approaches include convolutional neural networks (CNNs), 3D CNNs, long short-term memory networks (LSTM), or transformer-based models capable of learning long-range dependencies in behavior sequences. Additional feature extraction methods will be evaluated to integrate physiologic and environmental signals.
To avoid model overfitting and ensure generalizability, the dataset will be split into training, validation, and independent test sets. Cross-validation will be used during parameter tuning. Model output will include risk scores or prediction probabilities indicating the likelihood of an impending accidental event.
Performance will be evaluated using accuracy, sensitivity, specificity, F1 score, and lead time (the time interval between system alert and actual event). The lead-time metric is particularly important because practical utility in clinical care depends on whether alerts occur early enough for staff to intervene.
Outcome Interpretation This study does not impose any medical intervention on participants. All adverse events are part of routine clinical care; the study merely investigates whether AI can anticipate them. Through continuous monitoring and analytical modeling, the research aims to quantify how much predictive information is contained in patient behavior, movement patterns, and environmental context captured by video.
The findings will help determine the feasibility and clinical value of AI-assisted behavioral monitoring in real-world ICUs. If successful, such systems may provide early warnings of delirium, accidental device removal, or other behavior-linked risks. This may reduce emergency interventions, shorten ICU stays, and improve overall patient safety.
Follow-Up To understand the longer-term relevance of the AI predictions, patients will undergo follow-up assessments after discharge at 1 month and 6 months. Follow-up evaluates general health recovery, sleep status, cognition, and whether any delayed complications occurred. Patient and family feedback regarding video monitoring-including comfort level, perceived benefit, or privacy concerns-will also be collected to guide system refinement.
Ethical and Privacy Considerations The study emphasizes privacy protection and informed consent. Cameras are positioned to minimize exposure of unnecessary areas. De-identification is applied before analysis, and all data are managed within controlled hospital systems. Participants may withdraw at any point without affecting their care. The study involves no experimental treatment or additional medical procedures beyond standard ICU monitoring.
Scientific and Clinical Significance This research addresses a critical gap in ICU safety: behavior-based early warning. By combining AI, video analysis, physiology, and environmental data, the study explores an approach that could complement routine monitoring. Beyond predicting specific events, the project may contribute to broader understanding of ICU patient behavioral trajectories and the role of environmental factors such as noise.
The long-term vision is to create a clinically deployable system that supports early intervention, reduces preventable harm, and enhances the efficiency of ICU care.
- Conditions
- Behavioral Monitoring in ICU, Prediction of Accidental Events Using AI-Assisted Video Analysis, ICU Patient Safety and Early Warning System
- Being tested
- AI-Assisted Video Monitoring
- Keywords
- Delirium, Accidental Extubation, Unplanned Device Removal, Sleep Disturbance, Agitation in ICU Patients, Critical Illness
- Medical subject headings
- Delirium, Parasomnias, Critical Illness
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
AI-Assisted Video MonitoringOther
This intervention consists of continuous bedside video monitoring combined with routine physiologic data and environmental noise levels. A ceiling-mounted camera captures patient movements and posture without altering clinical care. All video is de-identified through face masking or avatar replacement, and background areas are blurred to protect privacy. Data are synchronized with vital signs and used solely for AI-based behavioral analysis to identify early patterns associated with delirium, agitation, sleep disruption, and accidental device removal. No treatments, medications, or clinical decisions are changed as part of this study. This intervention involves data collection only and does not modify standard ICU care
| Study group | Role | What they receive |
|---|---|---|
| Single Cohort | This cohort includes ICU patients who undergo continuous bedside video monitoring combined with routine vital-sign collection. Video, physiologic, and noise-level data are used for AI-based analysis to identify patterns associated with delirium, agitation, and accidental device removal. No clinical treatment or care procedures are altered. The study is observational and involves data collection only Receives: Other: AI-Assisted Video Monitoring |
What is being measured
The primary outcome is the main question the study is designed to answer.
Accuracy of AI-Assisted Video Monitoring in Predicting Accidental Events
Accuracy will be measured as the proportion of correct AI predictions compared with clinically confirmed accidental events, including delirium-related agitation, unplanned device removal, and significant sleep disruption. Accuracy includes both true positive and true negative predictions. The AI model's output will be compared with event labels validated through clinical documentation and human annotation of video data. This outcome assesses whether the AI system can reliably identify high-risk behavioral patterns before the occurrence of actual adverse events.
Measured: From ICU admission until ICU discharge (up to 30 days)
Secondary outcomes (3)
Sensitivity of AI Predictions for Accidental Events
Sensitivity will be calculated as the true positive rate: the proportion of actual accidental events that were correctly identified in advance by the AI system. Events include delirium-related agitation, attempts at device removal, and significant sleep disturbances. Sensitivity will be validated against clinician-confirmed events and annotated video data.
Measured: From ICU admission to ICU discharge (up to 30 days)
Specificity of AI Predictions
Specificity will measure the AI system's ability to correctly identify patients who did not experience accidental events. It is calculated as the proportion of true negative predictions among all non-event periods. High specificity indicates reduced false alarms and improved clinical usability.
Measured: From ICU admission to ICU discharge (up to 30 days)
Lead Time Between AI Alert and Actual Event
Lead time is defined as the time interval (in seconds) between the AI system generating an alert and the subsequent clinically confirmed accidental event. This outcome assesses whether the AI provides actionable early warnings that allow nurses to intervene before harm occurs. A minimum clinically meaningful lead time is expected to be ≥10 seconds.
Measured: From ICU admission to ICU discharge (up to 30 days)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Dec 2025
- Study start1 Jan 2026 (estimated)
- Primary completion31 Dec 2027 (estimated)
- Study completion31 Dec 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Behavioral Monitoring in ICUStudies of the same condition, open and under way.
- More trials run by Shanghai Zhongshan HospitalThe 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
- 300 participants (estimated)
- Target duration
- 7 Days
Sponsor and investigators
- Lead sponsor
- Shanghai Zhongshan Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07307521
- Sponsor's protocol ID
- B2024-512
- Acronym
- AIME-ICU
- Status last verified
- Dec 2025
- First submitted
- 13 Dec 2025
- Last updated
- 29 Dec 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 29 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Exploring the Use of AI-Assisted Video Monitoring to Predict Accidental Events in ICU Patients
- ClinicalTrials.gov ID
- NCT07307521
- Acronym / sponsor ID
- AIME-ICU / B2024-512
- Conditions
- Behavioral Monitoring in ICU, Prediction of Accidental Events Using AI-Assisted Video Analysis, ICU Patient Safety and Early Warning System
- Keywords
- Delirium, Accidental Extubation, Unplanned Device Removal, Sleep Disturbance, Agitation in ICU Patients, Critical Illness
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 300 participants (estimated)
- Lead sponsor
- Shanghai Zhongshan HospitalUniversity, hospital or other
- Study start
- 1 Jan 2026 (estimated)
- Primary completion
- 31 Dec 2027 (estimated)
- Study completion
- 31 Dec 2028 (estimated)
- First posted
- 29 Dec 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.
This study aims to improve the safety and care of patients in the Intensive Care Unit (ICU) by using artificial intelligence (AI) to analyze video monitoring. ICU patients often face serious risks such as delirium, accidental removal of breathing tubes or lines, and sleep problems. These events can lead to medical emergencies, longer ICU stays, higher costs, and worse outcomes.
To address these challenges, we will place a small video camera above each ICU bed. The camera will record patient movements, body activity, and sleep patterns. At the same time, routine medical monitors will record heart rate, blood oxygen levels, and other vital signs. Noise levels in the room will also be measured. All these data help us understand the patient's behavior and condition more accurately.
The video recording does not involve extra treatment or additional procedures. All data are collected passively and safely. Patient privacy is strictly protected: the system will blur faces or replace them with digital avatars, and any information that could identify the patient or the environment will be masked. All videos are stored securely inside the hospital and are processed only after privacy protection.
Using these recordings, an AI model will be trained to recognize early warning signs of dangerous situations. For example, the system may detect early movements that suggest the patient is becoming agitated, confused, or trying to remove medical tubes. It may also identify severe sleep disturbance that may lead to delirium. If the AI can recognize these early changes, medical staff can intervene sooner and prevent harm.
About 300 patients from Fudan University Zhongshan Hospital will participate. Participation is voluntary. Patients or families will sign an informed consent form before being enrolled. The study has three stages:
Screening - understanding the study and signing consent. Data collection - video and medical monitor data are collected during the ICU stay.
Follow-up - telephone or in-person follow-up at 1 month and 6 months after discharge to evaluate recovery, sleep, mental status, and overall safety.
There are no direct medical risks from participating in this study because it only collects behavioral and monitoring data. The cameras do not interfere with treatment. Privacy and data security are the main considerations, and all measures strictly follow national laws and hospital regulations.
Participants may benefit from earlier identification of dangerous situations, which may help prevent accidental tube removal, severe agitation, or other emergencies. Even if no direct benefit occurs, the information collected may help improve future ICU care by enabling safer and more accurate monitoring systems.
Taking part in the study will not affect the patient's medical care. Patients may withdraw at any time without any consequences or loss of benefits.
This study hopes to build a reliable AI tool that can assist nurses and doctors in recognizing early signs of trouble, improving safety, and enhancing the quality of care for ICU patients.
Detailed description
This study investigates whether artificial intelligence (AI)-assisted video monitoring can identify early behavioral changes that precede accidental or harmful events in Intensive Care Unit (ICU) patients. ICU patients are vulnerable to a series of sudden and potentially dangerous events-such as agitation, delirium, accidental device removal, and significant sleep disruption-many of which develop gradually and are difficult to detect solely from routine physiological monitoring. This project aims to determine whether AI analysis of continuous bedside video recordings, combined with noise-level information and vital-sign data already collected during standard ICU care, can provide clinicians with timely warnings before these events occur.
Rationale Traditional ICU monitoring systems focus on physiological parameters such as heart rate, blood pressure, and oxygen saturation. While essential, these measurements do not fully represent patient behavior. Many high-risk events are preceded by subtle motor patterns or behavioral cues-for example, repeated reaching toward tubes, rising restlessness, or disturbed sleep cycles. Such cues are often intermittent, brief, or masked by sedation or other treatments, making them difficult for staff to detect in busy clinical environments.
Computer vision and AI technologies offer an opportunity to objectively observe and interpret patient movements and behavioral trends continuously, without adding clinical workload. By integrating video information with physiologic data and environmental noise levels, the AI system may identify patterns that indicate emerging delirium, increased agitation, or imminent attempts to remove medical devices. Early identification may support timely preventive interventions and reduce the rates of adverse events.
Study Overview The study will prospectively enroll ICU patients who consent to video monitoring and data use. A small camera will be installed above each bed to continuously capture patient movement and posture. The camera view is restricted to the patient zone, excluding unnecessary areas such as the nursing station. All recordings follow strict privacy-protection procedures, including automated face masking, background blurring, and removal of identifying information from objects in the frame.
Environmental noise is recorded through a decibel meter, and routine vital-sign data are synchronized with the video timeline. These combined multimodal data will serve as input for AI model development.
The study is divided into three components:
Data collection phase - real-world continuous recording of behavioral and physiological data.
Data processing and annotation - cleaning, de-identification, and labeling of key behavioral events by trained researchers.
Model development and evaluation - training AI models to identify behavioral patterns associated with clinically meaningful events, and evaluating their predictive performance.
Data Integration and Processing
All raw videos remain stored securely inside the hospital's protected data environment and are not transferred outside. A standardized de-identification pipeline is applied before any analytical use. This includes:
Masking or replacing patient faces. Removing identifying elements such as bed numbers and equipment labels. Blurring all background areas outside the patient zone. Excluding frames containing staff faces or unrelated activities. After de-identification, videos are aligned with vital-sign and noise-level timelines to create multimodal time-series datasets. Human annotators, trained with a unified labeling guideline, identify episodes of agitation, possible delirium-related behavior, attempts at device removal, and sleep-wake transitions. These labels serve as ground truth for AI training.
AI Model Development Multiple AI architectures will be explored, particularly those suited for temporal video analysis. Potential approaches include convolutional neural networks (CNNs), 3D CNNs, long short-term memory networks (LSTM), or transformer-based models capable of learning long-range dependencies in behavior sequences. Additional feature extraction methods will be evaluated to integrate physiologic and environmental signals.
To avoid model overfitting and ensure generalizability, the dataset will be split into training, validation, and independent test sets. Cross-validation will be used during parameter tuning. Model output will include risk scores or prediction probabilities indicating the likelihood of an impending accidental event.
Performance will be evaluated using accuracy, sensitivity, specificity, F1 score, and lead time (the time interval between system alert and actual event). The lead-time metric is particularly important because practical utility in clinical care depends on whether alerts occur early enough for staff to intervene.
Outcome Interpretation This study does not impose any medical intervention on participants. All adverse events are part of routine clinical care; the study merely investigates whether AI can anticipate them. Through continuous monitoring and analytical modeling, the research aims to quantify how much predictive information is contained in patient behavior, movement patterns, and environmental context captured by video.
The findings will help determine the feasibility and clinical value of AI-assisted behavioral monitoring in real-world ICUs. If successful, such systems may provide early warnings of delirium, accidental device removal, or other behavior-linked risks. This may reduce emergency interventions, shorten ICU stays, and improve overall patient safety.
Follow-Up To understand the longer-term relevance of the AI predictions, patients will undergo follow-up assessments after discharge at 1 month and 6 months. Follow-up evaluates general health recovery, sleep status, cognition, and whether any delayed complications occurred. Patient and family feedback regarding video monitoring-including comfort level, perceived benefit, or privacy concerns-will also be collected to guide system refinement.
Ethical and Privacy Considerations The study emphasizes privacy protection and informed consent. Cameras are positioned to minimize exposure of unnecessary areas. De-identification is applied before analysis, and all data are managed within controlled hospital systems. Participants may withdraw at any point without affecting their care. The study involves no experimental treatment or additional medical procedures beyond standard ICU monitoring.
Scientific and Clinical Significance This research addresses a critical gap in ICU safety: behavior-based early warning. By combining AI, video analysis, physiology, and environmental data, the study explores an approach that could complement routine monitoring. Beyond predicting specific events, the project may contribute to broader understanding of ICU patient behavioral trajectories and the role of environmental factors such as noise.
The long-term vision is to create a clinically deployable system that supports early intervention, reduces preventable harm, and enhances the efficiency of ICU care.
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Target follow-up
- 7 Days
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Single Cohort | – | Other: AI-Assisted Video MonitoringThis cohort includes ICU patients who undergo continuous bedside video monitoring combined with routine vital-sign collection. Video, physiologic, and noise-level data are used for AI-based analysis to identify patterns associated with delirium, agitation, and accidental device removal. No clinical treatment or care procedures are altered. The study is observational and involves data collection only |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- The study population consists of ICU patients who undergo continuous bedside monitoring as part of routine critical care. Participants include adults and pediatric patients admitted to a mixed medical-surgical ICU. Individuals are enrolled only after informed consent is obtained from the patient or a legally authorized representative. The cohort represents typical ICU patients at risk for behavioral or accidental events such as agitation, delirium, sleep disturbance, or unplanned device removal. The population reflects real-world conditions and clinical diversity, allowing evaluation of AI-assisted video monitoring across a broad range of critical illness severity and diagnoses.
Key inclusion criteria (4 listed)
- Adult or pediatric patients admitted to the Intensive Care Unit (ICU).
- Patient or legally authorized representative is capable of understanding the study information and providing informed consent.
- Patient is expected to remain in the ICU long enough to allow video and physiologic data collection.
- Agreement to participate and allow video monitoring during the ICU stay.
Key exclusion criteria (5 listed)
- Refusal to participate from the patient or legally authorized representative.
- Patients for whom continuous video monitoring is medically inappropriate or not feasible (e.g., isolation conditions preventing camera installation).
- Patients whose condition or legal status requires special restrictions on video recording (e.g., certain forensic or custodial cases).
- Any situation judged by the clinical team to place the patient at increased privacy or safety risk by participation.
- Withdrawal of consent at any point during the study.
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 |
|---|---|---|
| AI-Assisted Video MonitoringThis intervention consists of continuous bedside video monitoring combined with routine physiologic data and environmental noise levels. A ceiling-mounted camera captures patient movements and posture without altering clinical care. All video is de-identified through face masking or avatar replacement, and background areas are blurred to protect privacy. Data are synchronized with vital signs and used solely for AI-based behavioral analysis to identify early patterns associated with delirium, agitation, sleep disruption, and accidental device removal. No treatments, medications, or clinical decisions are changed as part of this study. This intervention involves data collection only and does not modify standard ICU care | Other | Single Cohort |
Primary outcome
Accuracy of AI-Assisted Video Monitoring in Predicting Accidental Events
Time frame: From ICU admission until ICU discharge (up to 30 days)
Accuracy will be measured as the proportion of correct AI predictions compared with clinically confirmed accidental events, including delirium-related agitation, unplanned device removal, and significant sleep disruption. Accuracy includes both true positive and true negative predictions. The AI model's output will be compared with event labels validated through clinical documentation and human annotation of video data. This outcome assesses whether the AI system can reliably identify high-risk behavioral patterns before the occurrence of actual adverse events.
3 secondary outcomes
Sensitivity of AI Predictions for Accidental Events
Time frame: From ICU admission to ICU discharge (up to 30 days)
Specificity of AI Predictions
Time frame: From ICU admission to ICU discharge (up to 30 days)
Lead Time Between AI Alert and Actual Event
Time frame: From ICU admission to ICU discharge (up to 30 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 29 Dec 2025.
- Individual participant dataSharing planned: Undecided
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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.
Questions about this trial
What is this clinical trial studying?
An observational study of Behavioral Monitoring in ICU and Prediction of Accidental Events Using AI-Assisted Video Analysis, run by Shanghai Zhongshan Hospital.
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 4 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 29 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
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 Gu zhunyong, Gu (8613918677995, gu.zhunyong@zs-hospital.sh.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Accuracy of AI-Assisted Video Monitoring in Predicting Accidental Events (time frame: From ICU admission until ICU discharge (up to 30 days)). 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 29 Dec 2025.