Sudden Cardiac ArrestNCT07452016
AI-guided Prediction and Treatment of Cardiac Arrest
A study testing Machine learning-guided cardiac arrest prediction device in people with Sudden Cardiac Arrest, run by MetroHealth Medical Center at 1 site in United States.
Trial summary
Sudden cardiac arrest is a major health problem, and most people don't survive. One big reason is that even if resuscitation is successful, people commonly have recurrent cardiac arrests (rearrest). Right now, it is not possible to accurately predict a rearrest or prevent it. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Sudden Cardiac Arrest
- What is being tested?
- Machine learning-guided cardiac arrest prediction device
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 68 participants
- Where
- 1 siteUnited States
- Study dates
- Aug 2026to Jun 2029
- Phase
- Interventional
- 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 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Adult (18 years of age or older) EMS providers (Simulation trial)
- Adult (18 years of age or older) patients have attempted resuscitation from out-of-hospital SCA of any etiology (Clinical trail)
Who cannot join
- Non-English-speaking providers
- Providers who do not care for cardiac arrest patients
- Prisoners
- Pediatric patients under age of 18
- DNR/DNI
- No resuscitation attempted (declared deceased in field by EMS)
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
The MetroHealth System
Cleveland, Ohio, 44109
Lance Wilson Attending Physician and Professor, Emergency Medicine, MD, 216-978-6274, lwilson@metrohealth.org
Julie Nichols Research Coordinator, RN, (216) 957-6488, jnichols@metrohealth.org
About this study
Official title: Improving Cardiac Arrest Outcomes Using Artificial Intelligence Guided Precision Treatments
Sudden cardiac arrest is a major health problem, and most people don't survive. One big reason is that even if resuscitation is successful, people commonly have recurrent cardiac arrests (rearrest). Right now, it is not possible to accurately predict a rearrest or prevent it. The investigators have developed a machine learning device that uses the heart tracing (ECG) to predict when and why a rearrest occurs. The investigators plan to test if it will accurately and effectively help EMS providers predict rearrest and provide timely treatment to increase survival after cardiac arrest. To determine if this machine learning device will work in the real world, the investigators need to find out if there are barriers to using it, and whether EMS providers will think it is useful and will help them improve the care of patients who have a cardiac arrest. The investigators will first test the device in live simulated cardiac arrest scenarios to see if the providers can use it and if they find the device potentially valuable in taking care of patients. In a second study, the investigators will test how accurate the device is in predicting if a cardiac arrest will happen again in patients who have just been brought back to life after a cardiac arrest. EMS providers will attach the device, but it will only work in the background. EMS will take care of patients as they normally would, without using or knowing what the device says. To see if the device is accurate at predicting another cardiac arrest, the investigators will analyze the results offline, and compare what the device says to what actually happens to the patient. By comparing what the device predicts to what actually happens, the investigators can see how well it predicts another cardiac arrest and estimate how it might improve treatment of patients.
Read the detailed description
Sudden cardiac arrest (SCA) remains a major cause of mortality in the United States. Despite significant efforts to improve resuscitation outcomes, survival remains poor. Moreover, SCA is often the first manifestation of underlying heart disease, after which survivors typically suffer secondary chronic cardiovascular and neurological disease due to the primary insult. Resuscitation from SCA is initiated in patients suffering from life-threatening arrhythmias, generally ventricular tachycardia/fibrillation (VT/VF) or pulseless electrical activity (PEA), that if successful, is followed by a return of spontaneous circulation (ROSC). This, however, is commonly followed by repeated rearrest due to either VT/VF, PEA, or asystole. Importantly, the mechanisms of VT/VF and PEA vary significantly, and protocolized, non-directed treatments can worsen outcomes. Currently, treatments are typically initiated after rearrest occurs and without regard to an individual patient's unique personal or arrest characteristics, factors which are known predictors of cardiac arrest outcomes. Recent studies have shown that a quicker and more targeted treatment response (i.e., shorter time to treat with rearrest type-specific treatment) for cardiac arrest can significantly improve survival and downstream chronic sequelae after SCA. Therefore, the ability to predict cardiac arrest or rearrest occurrence and cause (i.e. VT/VF and PEA) could guide early personalized therapy and ultimately improve resuscitation outcomes, which is the long-term translational goal of this effort. Additionally, early intervention could be critical in rural communities, where transport times to definitive hospital care are long, and resources are limited.
In ongoing work the investigators have recently observed in emergency medical services (EMS) patients that adding clinical parameters (e.g., age, primary arrest type) to features derived from the ECG T-wave in a machine learning (ML) model improves prediction accuracy of VT/VF and PEA (>90%). The investigators propose a feasibility study of ML-guided prediction of rearrest. The overall hypothesis is that an ECG biomarker, combined with clinical features, can predict rearrest and its cause (VT/VF or PEA), which will significantly improve time to treatment and cardiac arrest acute and chronic outcomes. The investigators further hypothesize that such technology can be readily adopted and successfully implemented by emergency responders. The investigators plan two interrelated clinical trials, one an observational trial in simulated cardiac arrest, and a second observational trial in EMS patients. The following specific aims will test these hypotheses.
Aim 1. Determine end-user performance and satisfaction with a fully automated ML-guided rearrest prediction device using simulated cardiac arrest scenarios. Emergency providers, in simulated real-time resuscitation scenarios using real rearrest ECG recordings will be studied to identify barriers and facilitators to technology implementation and adoption, as well as provider satisfaction and the perceived value of the intervention. This will be achieved by determining provider performance metrics (e.g., initiating ML-guided therapies) and using qualitative tools to assess end-user engagement, trust and perceived utility. These studies will provide foundational data for the implementation and scalability of the technology for both a clinical trial and guidance for future FDA and regulatory approval.
Aim 2. Test the accuracy of a multiclass ML model for real-time prediction of rearrest occurrence and its type (VT/VF vs. PEA) and impact on time to treatment, in an observational clinical trial of cardiac arrest patients. Leveraging an ongoing collaboration with Cleveland and community EMS, the investigators will enroll EMS cardiac arrest patients and observe for the occurrence of rearrest in a proof-of-concept observational validation study. The accuracy of the fully automated ML model to predict rearrest and its type will be determined, but treatment guidance will not be tested at this time. Providers will be blinded to the ML output, and ML will not direct treatment. Offline, prediction accuracy and estimated time to ML-guided treatment decision will be compared to actual rearrest type and time of treatment. These results will provide preliminary safety and accuracy results, sample size estimates, and recruitment and informed consent processes for a future randomized controlled clinical trial to test ML-guided rearrest treatments.
- Conditions
- Sudden Cardiac Arrest
- Being tested
- Machine learning-guided cardiac arrest prediction device
- Keywords
- cardiac arrest, sudden cardiac death, machine learning, rearrest, ventricular fibrillation, ventricular tachycardia, pulseless electrical activity
- Medical subject headings
- Death, Sudden, Cardiac, Heart Arrest, Ventricular Fibrillation, Tachycardia, Ventricular
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Machine learning-guided cardiac arrest prediction deviceDevice
A machine learning-guided cardiac arrest prediction device will be used to predict recurrence of cardiac arrest after initially successful resuscitation. It will also predict if the recurrent cardiac arrest is caused by ventricular fibrillation/tachycardia or pulseless electrical activity.
| Study group | Role | What they receive |
|---|---|---|
| Emergency Medical Service Providers | Experimental | Emergency Medical Service Providers will experience high fidelity cardiac arrest simulations and test the barriers and facilitators to using a machine learning guided prediction device in simulated cardiac arrest patients. Receives: Device: Machine learning-guided cardiac arrest prediction device |
| Patients who experience cardiac arrest cared for by EMS | Other | Patients who experience cardiac arrest will receive normal standard of care treatments. A machine learning guided prediction device will run in the background and also receive the normally acquired ECG data. Offline, the accuracy of the device to predict recurrent cardiac arrest and the type of rearrest which occurs after successful return of spontaneous circulation will be determined. Receives: Device: Machine learning-guided cardiac arrest prediction device |
What is being measured
The primary outcome is the main question the study is designed to answer.
Mean Implementation Acceptability Score
Mean score on a 20-item post-simulation survey adapted from the Consolidated Framework for Implementation Research (CFIR). Each item is rated on a 5-point Likert scale from 1 (strongly disagree) to 5 (strongly agree). The composite score is calculated as the mean of all items (range 1-5), with higher scores indicating greater perceived implementation acceptability.
Measured: Assessed once immediately after completion of the simulation session (within 5 hours of enrollment).
Calculated time to treatment benefit
Determination of estimated change in time to treatments for cardiac arrest patients from the observational clinical trial of the ML-guided prediction device. Time to treatment will be measured (in seconds) from time to EMS arrival at scene to treatment time for the first rearrest is rendered. This will be compared to calculated time to treatment, measured from EMS arrival to machine learning prediction (in seconds).
Measured: From subject enrollment up to 2 hours
Secondary outcomes (3)
Accuracy of ML-guided rearrest predication
Standard accuracy measures of device predication will performance in the phase 2 observational clinical trial. Machine learning prediction of rearrest occurrence and rhythm type will be compared to the actual observed rearrest occurrence and rhythm type. Accuracy will be defined as the percentage of correct predictions (True Positives + True Negatives) over the total dataset and shown in a confusion matrix.
Measured: From subject enrollment up to 2 hours
Time to machine learning guided prediction
Time to machine learning prediction of rearrest will be performed in the observational clinical trial of the ML-guided prediction device. Time to prediction will be measured (in seconds) from the time of EMS arrival to time the machine learning prediction device predicts the first rearrest with confidence greater than or equal to 70%.
Measured: From subject enrollment up to 2 hours
Time to device deployment in simulated cardiac arrest
Time to machine learning device deployment will be measured in cardiac arrest simulations. Time to deploy the device in simulated cardiac arrest patients will be measured (in seconds) from the time of simulated EMS arrival to time the machine learning prediction device is deployed and begins to collect data.
Measured: Assessed once immediately after completion of the simulation session (within 5 hours of enrollment).
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Mar 2026
- Study startAug 2026 (estimated)
- Primary completionJun 2029 (estimated)
- Study completionJun 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Sudden Cardiac ArrestStudies of the same condition, open and under way.
- 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 68 participants (estimated)
Sponsor and investigators
- Lead sponsor
- MetroHealth Medical Center
- Sponsor type
- University, hospital or other
- Collaborators
- National Center for Advancing Translational Sciences (NCATS)
- Responsible party
- Principal investigator, Lance Wilson, MetroHealth Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07452016
- Sponsor's protocol ID
- STUDY00001031
- Other IDs
- UM1TR004528
- Status last verified
- Mar 2026
- First submitted
- 17 Feb 2026
- Last updated
- 16 Mar 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Deidentified demographic and outcome data. Model outcome data.
Study at a glance
From the registry record, last updated by the sponsor on 16 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Improving Cardiac Arrest Outcomes Using Artificial Intelligence Guided Precision Treatments
- ClinicalTrials.gov ID
- NCT07452016
- Acronym / sponsor ID
- STUDY00001031
- Conditions
- Sudden Cardiac Arrest
- Keywords
- cardiac arrest, sudden cardiac death, machine learning, rearrest, ventricular fibrillation, ventricular tachycardia, pulseless electrical activity
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 68 participants (estimated)
- Lead sponsor
- MetroHealth Medical CenterUniversity, hospital or other
- Collaborators
- National Center for Advancing Translational Sciences (NCATS)
- Study start
- Aug 2026 (estimated)
- Primary completion
- Jun 2029 (estimated)
- Study completion
- Jun 2029 (estimated)
- First posted
- 5 Mar 2026 (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.
Sudden cardiac arrest is a major health problem, and most people don't survive. One big reason is that even if resuscitation is successful, people commonly have recurrent cardiac arrests (rearrest). Right now, it is not possible to accurately predict a rearrest or prevent it. The investigators have developed a machine learning device that uses the heart tracing (ECG) to predict when and why a rearrest occurs. The investigators plan to test if it will accurately and effectively help EMS providers predict rearrest and provide timely treatment to increase survival after cardiac arrest. To determine if this machine learning device will work in the real world, the investigators need to find out if there are barriers to using it, and whether EMS providers will think it is useful and will help them improve the care of patients who have a cardiac arrest. The investigators will first test the device in live simulated cardiac arrest scenarios to see if the providers can use it and if they find the device potentially valuable in taking care of patients. In a second study, the investigators will test how accurate the device is in predicting if a cardiac arrest will happen again in patients who have just been brought back to life after a cardiac arrest. EMS providers will attach the device, but it will only work in the background. EMS will take care of patients as they normally would, without using or knowing what the device says. To see if the device is accurate at predicting another cardiac arrest, the investigators will analyze the results offline, and compare what the device says to what actually happens to the patient. By comparing what the device predicts to what actually happens, the investigators can see how well it predicts another cardiac arrest and estimate how it might improve treatment of patients.
Detailed description
Sudden cardiac arrest (SCA) remains a major cause of mortality in the United States. Despite significant efforts to improve resuscitation outcomes, survival remains poor. Moreover, SCA is often the first manifestation of underlying heart disease, after which survivors typically suffer secondary chronic cardiovascular and neurological disease due to the primary insult. Resuscitation from SCA is initiated in patients suffering from life-threatening arrhythmias, generally ventricular tachycardia/fibrillation (VT/VF) or pulseless electrical activity (PEA), that if successful, is followed by a return of spontaneous circulation (ROSC). This, however, is commonly followed by repeated rearrest due to either VT/VF, PEA, or asystole. Importantly, the mechanisms of VT/VF and PEA vary significantly, and protocolized, non-directed treatments can worsen outcomes. Currently, treatments are typically initiated after rearrest occurs and without regard to an individual patient's unique personal or arrest characteristics, factors which are known predictors of cardiac arrest outcomes. Recent studies have shown that a quicker and more targeted treatment response (i.e., shorter time to treat with rearrest type-specific treatment) for cardiac arrest can significantly improve survival and downstream chronic sequelae after SCA. Therefore, the ability to predict cardiac arrest or rearrest occurrence and cause (i.e. VT/VF and PEA) could guide early personalized therapy and ultimately improve resuscitation outcomes, which is the long-term translational goal of this effort. Additionally, early intervention could be critical in rural communities, where transport times to definitive hospital care are long, and resources are limited.
In ongoing work the investigators have recently observed in emergency medical services (EMS) patients that adding clinical parameters (e.g., age, primary arrest type) to features derived from the ECG T-wave in a machine learning (ML) model improves prediction accuracy of VT/VF and PEA (>90%). The investigators propose a feasibility study of ML-guided prediction of rearrest. The overall hypothesis is that an ECG biomarker, combined with clinical features, can predict rearrest and its cause (VT/VF or PEA), which will significantly improve time to treatment and cardiac arrest acute and chronic outcomes. The investigators further hypothesize that such technology can be readily adopted and successfully implemented by emergency responders. The investigators plan two interrelated clinical trials, one an observational trial in simulated cardiac arrest, and a second observational trial in EMS patients. The following specific aims will test these hypotheses.
Aim 1. Determine end-user performance and satisfaction with a fully automated ML-guided rearrest prediction device using simulated cardiac arrest scenarios. Emergency providers, in simulated real-time resuscitation scenarios using real rearrest ECG recordings will be studied to identify barriers and facilitators to technology implementation and adoption, as well as provider satisfaction and the perceived value of the intervention. This will be achieved by determining provider performance metrics (e.g., initiating ML-guided therapies) and using qualitative tools to assess end-user engagement, trust and perceived utility. These studies will provide foundational data for the implementation and scalability of the technology for both a clinical trial and guidance for future FDA and regulatory approval.
Aim 2. Test the accuracy of a multiclass ML model for real-time prediction of rearrest occurrence and its type (VT/VF vs. PEA) and impact on time to treatment, in an observational clinical trial of cardiac arrest patients. Leveraging an ongoing collaboration with Cleveland and community EMS, the investigators will enroll EMS cardiac arrest patients and observe for the occurrence of rearrest in a proof-of-concept observational validation study. The accuracy of the fully automated ML model to predict rearrest and its type will be determined, but treatment guidance will not be tested at this time. Providers will be blinded to the ML output, and ML will not direct treatment. Offline, prediction accuracy and estimated time to ML-guided treatment decision will be compared to actual rearrest type and time of treatment. These results will provide preliminary safety and accuracy results, sample size estimates, and recruitment and informed consent processes for a future randomized controlled clinical trial to test ML-guided rearrest treatments.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Emergency Medical Service Providers | Experimental | Device: Machine learning-guided cardiac arrest prediction deviceEmergency Medical Service Providers will experience high fidelity cardiac arrest simulations and test the barriers and facilitators to using a machine learning guided prediction device in simulated cardiac arrest patients. |
| Patients who experience cardiac arrest cared for by EMS | Other | Device: Machine learning-guided cardiac arrest prediction devicePatients who experience cardiac arrest will receive normal standard of care treatments. A machine learning guided prediction device will run in the background and also receive the normally acquired ECG data. Offline, the accuracy of the device to predict recurrent cardiac arrest and the type of rearrest which occurs after successful return of spontaneous circulation will be determined. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Adult (18 years of age or older) EMS providers (Simulation trial)
- Adult (18 years of age or older) patients have attempted resuscitation from out-of-hospital SCA of any etiology (Clinical trail)
Key exclusion criteria (6 listed)
- Non-English-speaking providers
- Providers who do not care for cardiac arrest patients
- Prisoners
- Pediatric patients under age of 18
- DNR/DNI
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 |
|---|---|---|
| Machine learning-guided cardiac arrest prediction deviceA machine learning-guided cardiac arrest prediction device will be used to predict recurrence of cardiac arrest after initially successful resuscitation. It will also predict if the recurrent cardiac arrest is caused by ventricular fibrillation/tachycardia or pulseless electrical activity. | Device | Emergency Medical Service Providers, Patients who experience cardiac arrest cared for by EMS |
Primary outcome
Mean Implementation Acceptability Score
Time frame: Assessed once immediately after completion of the simulation session (within 5 hours of enrollment).
Mean score on a 20-item post-simulation survey adapted from the Consolidated Framework for Implementation Research (CFIR). Each item is rated on a 5-point Likert scale from 1 (strongly disagree) to 5 (strongly agree). The composite score is calculated as the mean of all items (range 1-5), with higher scores indicating greater perceived implementation acceptability.
Calculated time to treatment benefit
Time frame: From subject enrollment up to 2 hours
Determination of estimated change in time to treatments for cardiac arrest patients from the observational clinical trial of the ML-guided prediction device. Time to treatment will be measured (in seconds) from time to EMS arrival at scene to treatment time for the first rearrest is rendered. This will be compared to calculated time to treatment, measured from EMS arrival to machine learning prediction (in seconds).
3 secondary outcomes
Accuracy of ML-guided rearrest predication
Time frame: From subject enrollment up to 2 hours
Time to machine learning guided prediction
Time frame: From subject enrollment up to 2 hours
Time to device deployment in simulated cardiac arrest
Time frame: Assessed once immediately after completion of the simulation session (within 5 hours of enrollment).
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 16 Mar 2026.
- Individual participant dataSharing planned: Yes. Deidentified demographic and outcome data. Model outcome data.
Related trials for Sudden Cardiac Arrest
RecruitingObservational study
AI-powered ECG Analysis Using Willem™ Software in High-risk Cardiac Patients (WILLEM)
Cardiomyopathies, Cardiac Arrest
Active, not recruiting
Assessment of Combined CCM and ICD Device in HFrEF
Heart Failure, Heart Failure With Reduced Ejection Fraction
RecruitingObservational study
Genetic Markers of Cardiovascular Disease in Epilepsy
Epilepsy, Seizures
RecruitingObservational study
Observational Study of Cardiac Arrhythmias During Treatment With BTK Inhibitors or Venetoclax
Chronic Lymphocytic Leukemia (CLL), Waldenstr(SqrRoot)(Delta)m s Macroglobulinemia
Not yet recruitingObservational study
Cardiovascular Pre-participation Screening in Children and Adolescents
Sudden Cardiac Death, Cardiac Arrhythmias
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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Machine learning-guided cardiac arrest prediction device in people with Sudden Cardiac Arrest, run by MetroHealth Medical Center 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 2 inclusion and 6 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 16 Mar 2026. 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 Lance Wilson, MD (12169786274, lwilson@metrohealth.org), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Mean Implementation Acceptability Score (time frame: Assessed once immediately after completion of the simulation session (within 5 hours of enrollment).). The study lists 2 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 16 Mar 2026.