AI-ECG for Time-Resolved Prediction of HFrEF

April 2, 2026 updated by: Shanghai Zhongshan Hospital

Electrocardiogram-Based Deep Learning for Time-Resolved Prediction of Heart Failure With Reduced Ejection Fraction: A Multinational Study

This study aims to develop and validate a deep learning-based electrocardiogram (ECG) model for predicting the future risk of heart failure with reduced ejection fraction (HFrEF). The model is trained using raw 12-lead ECG data and generates individualized, time-resolved risk estimates over a 5-year period.

Data are obtained from multiple cohorts, including Zhongshan Hospital, Shanghai Tenth People's Hospital, and Beth Israel Deaconess Medical Center, representing diverse populations across China and the United States. The model is designed to identify individuals at elevated risk of developing HFrEF before the onset of overt clinical disease.

The performance of the model is evaluated using multiple complementary metrics, including discrimination, calibration, and clinical utility. In addition, interpretability analyses are conducted to explore the physiological relevance of ECG features associated with predicted risk.

This study seeks to provide an accessible and scalable tool for early risk stratification of heart failure, with the potential to support timely clinical decision-making and improve patient outcomes.

Study Overview

Detailed Description

Heart failure with reduced ejection fraction (HFrEF) is associated with substantial morbidity and mortality worldwide, and early identification of individuals at risk remains a major clinical challenge. Although existing risk models and biomarkers can provide prognostic information, their application is often limited by the need for laboratory testing or imaging, as well as variability in performance across populations.

In this study, we develop a deep learning-based survival model using raw 12-lead electrocardiogram (ECG) data to predict the future onset of HFrEF. The model is designed to generate individualized, time-to-event risk estimates over a 5-year follow-up period, allowing for dynamic assessment of risk trajectories rather than static classification.

The model is trained on data from Zhongshan Hospital and externally validated in independent cohorts from Shanghai Tenth People's Hospital and Beth Israel Deaconess Medical Center. These cohorts include a broad spectrum of patients, ranging from individuals without known cardiovascular disease to those with diverse clinical conditions, thereby enabling evaluation of model generalizability across different healthcare systems and demographic subgroups.

Model performance is comprehensively assessed using multiple metrics, including the concordance index, time-dependent area under the receiver operating characteristic curve, area under the precision-recall curve, Brier score, calibration analysis, and decision curve analysis. Risk stratification capability is evaluated using Kaplan-Meier survival analysis.

To enhance interpretability, complementary representation-based and attention-based methods are applied. These include variational autoencoder-derived latent feature analysis, correlation with conventional ECG parameters, and gradient-based visualization techniques to identify waveform regions contributing to model predictions. These approaches aim to ensure that the model captures physiologically meaningful signals associated with myocardial remodeling and cardiac dysfunction.

This study is observational and retrospective in nature and does not involve any intervention. The findings aim to support the development of a non-invasive, cost-effective, and widely accessible tool for early detection of individuals at risk of HFrEF, with potential implications for preventive strategies and personalized clinical management.

Study Type

Observational

Enrollment (Actual)

286709

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, China, 200436

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Participants were derived from three independent cohorts, including Zhongshan Hospital, Shanghai Tenth People's Hospital, and Beth Israel Deaconess Medical Center. The study population included adult patients who underwent routine ECG and echocardiographic evaluation in real-world clinical settings.

Description

Inclusion Criteria:

Adults aged ≥18 years Underwent standard 12-lead electrocardiography (ECG) Underwent transthoracic echocardiography with available LVEF measurement Availability of paired ECG-echocardiography data Data available for follow-up assessment

Exclusion Criteria:

Missing or incomplete ECG or echocardiography data Poor-quality ECG recordings unsuitable for analysis Missing key clinical variables required for model development

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Overall Study Population
Participants from three independent cohorts (Zhongshan Hospital, Shanghai Tenth People's Hospital, and Beth Israel Deaconess Medical Center) who underwent standard 12-lead electrocardiography and echocardiographic evaluation. These data were used to develop and externally validate a deep learning model for time-to-event prediction of incident heart failure with reduced ejection fraction (HFrEF). No interventions were assigned, as this was an observational study based on routinely collected clinical data.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incident Heart Failure With Reduced Ejection Fraction (HFrEF)
Time Frame: Up to 5 years
Occurrence of heart failure with reduced ejection fraction (HFrEF), defined as a left ventricular ejection fraction (LVEF) ≤40% during follow-up, as determined by transthoracic echocardiography. Both prevalent and incident cases identified from ECG-echocardiography data are included.
Up to 5 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2014

Primary Completion (Actual)

December 1, 2023

Study Completion (Actual)

December 1, 2023

Study Registration Dates

First Submitted

April 2, 2026

First Submitted That Met QC Criteria

April 2, 2026

First Posted (Actual)

April 9, 2026

Study Record Updates

Last Update Posted (Actual)

April 9, 2026

Last Update Submitted That Met QC Criteria

April 2, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

This study uses retrospective clinical data that are not publicly shareable.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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