Using Artificial Intelligence to Guide Chest Compressions During CPR for Adults with Out-of-Hospital Cardiac Arrest
Led by Far Eastern Memorial Hospital · Updated on 2026-02-24
255
Participants Needed
1
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
Researchers are exploring a new way to improve survival for adults who experience out-of-hospital cardiac arrest OHCA. This study focuses on using artificial intelligence AI to guide chest compressions during cardiopulmonary resuscitation CPR. Currently, chest compressions follow a standard location, but this may compress the aortic valve in nearly half of patients, reducing the chance of successful resuscitation. The study aims to develop an AI tool that analyzes arterial pressure waveforms in real time to identify the best compression site, shifting CPR towards a more personalized approach.
The study involves developing and validating an AI-Enhanced Arterial Waveform Monitor, based on advanced deep learning techniques, including YOLO v8. The project has five phases collecting data from 150 patients, creating algorithms to detect compression waveforms, training the AI to recognize aortic valve compression using patient data, clinically testing the AI on 75 additional patients, and finally assessing the AIs use as a real-time support app in 30 clinical cases. When the AI detects valve compression, rescuers adjust the chest compression position, usually downward and to the left, to improve blood flow.
Participants are adults aged 20 or older with non-traumatic OHCA receiving advanced life support. The study collects detailed physiological data, including arterial pressure and transesophageal echocardiography TEE images, to train and test the AI. Outcomes measured include how accurately the AI identifies valve compression, success at repositioning compressions, time taken for adjustments, return of spontaneous circulation ROSC, neurologic outcome at discharge, and chest compression metrics. The study spans about three years, with data collection, AI development, clinical testing, and real-world feasibility assessment phases.
CONDITIONS
Brief Title
The AIR-CPR Study: AI-Guided Chest Compressions
Research Team
S
Sheng-En Chu, physician
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Patients requiring Resuscitative Endovascular Balloon Occlusion of the Aorta (REBOA)
Cardiac arrest caused by massive hemorrhage, aortic emergencies, tension pneumothorax, cardiac tamponade, or pulmonary embolism
History of severe aortic valve disease or previous aortic valve surgery
Patients for whom TEE or femoral arterial catheterization is contraindicated
Situations where the medical team is unable to perform TEE or femoral arterial catheterization during CPR
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Monitoring
Duration - Up to approximately 30 days from emergency department resuscitation
Participants are monitored during cardiopulmonary resuscitation (CPR) with continuous arterial pressure waveform data collection and transesophageal echocardiography (TEE) to provide gold standard verification for AI model training and validation.
Continuous monitoring during CPR and emergency care
Implementation
Duration - During emergency department resuscitation period
The AI-Enhanced Arterial Waveform Monitor (AIR-CPR App) analyzes arterial pressure waveforms in real-time to guide rescuers on chest compression positioning to avoid aortic valve compression and optimize cardiac output during resuscitation efforts.
Real-time use during resuscitation events
Follow-up
Duration - Up to approximately 30 days after resuscitation
Participants are followed for outcomes including return of spontaneous circulation (ROSC), survival to discharge, and neurological status up to hospital discharge.
Approximately 1 to 2 visits during hospital stay
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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