AzTrials
AzTrials

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.

Not yet recruiting

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

Sites and contacts
Official record
Search all trials

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.

Lance Wilson, MD contact

12169786274

lwilson@metrohealth.org

Julie Nichols Research Coordinator, RN contact

(216) 957-6488

jnichols@metrohealth.org

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

Other trials in United States

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.

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 groups in NCT07452016
Study groupRoleWhat they receive
Emergency Medical Service ProvidersExperimentalEmergency 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 EMSOtherPatients 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.

  1. 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).

  2. 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)
  1. 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

  2. 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

  3. 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.

  1. First posted5 Mar 2026
  2. Study startAug 2026 (estimated)
  3. Primary completionJun 2029 (estimated)
  4. Study completionJun 2029 (estimated)

Resources

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)
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.

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.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in