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NOrthwestern Tempus AI-enaBLed Electrocardiography (NOTABLE) Trial

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Northwestern University

Status

Enrolling

Conditions

Arrhythmia
Atrial Fibrillation
Valvular Disease
Cardiovascular Diseases

Treatments

Device: Risk-Based Assessment for Cardiac Dysfunction

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT06511505
STU00220862

Details and patient eligibility

About

The goal of this clinical trial is to determine if a machine learning/artificial intelligence (AI)-based electrocardiogram (ECG) algorithm (rECHOmmend and ECG-AF) can identify undiagnosed cardiovascular disease in patients. It will also examine the safety and effectiveness of using this AI-based tool in a clinical setting. The main questions it aims to answer are:

  1. Can the AI-based ECG algorithm improve the detection of atrial fibrillation and structural heart disease?
  2. How does the use of this algorithm affect clinical decision-making and patient outcomes?

Researchers will compare the outcomes of healthcare providers who receive the AI-based ECG results to those who do not. Participants (healthcare providers) will:

Be randomized into two groups: one that receives AI-based ECG results and one that does not.

In the intervention group, receive an assessment of their patient's risk of atrial fibrillation or structural heart disease with each ordered ECG.

Decide whether to perform further clinical evaluation based on the AI-generated risk assessment as part of routine clinical care.

Full description

There is a large burden of undiagnosed, treatable cardiovascular disease (CVD), encompassing various heart conditions such as arrhythmias (e.g., atrial fibrillation) and structural heart diseases (e.g., valvular disease). Early detection and accurate diagnosis can significantly improve patient outcomes by enabling timely, guideline-based interventions or therapies.

The goal of this study is to leverage machine learning approaches to enhance the detection and diagnosis of CVD. By identifying patients at risk of undiagnosed CVD and referring them for further clinical evaluation, the study aims to improve health outcomes.

Study Overview:

The NOTABLE study will compare the rates of new disease diagnoses, therapeutic interventions, and cardiovascular outcomes between two groups of patients managed by clinicians at Northwestern Medicine:

Patients whose clinicians use ECG predictive models. Patients whose clinicians do not use ECG predictive models.

Intervention Details:

This study utilizes Tempus AI algorithms (rECHOmmend and ECG-AF) to analyze 12-lead ECGs. Clinicians randomized to the intervention group will receive a "Risk-Based Assessment for Cardiac Dysfunction" when ordering a 12-lead ECG within EPIC. If a high-risk result is identified, clinicians receive an EHR inbox message suggesting a follow-up diagnostic test, such as echocardiography and/or ambulatory ECG monitoring.

Outcome Tracking:

Weekly summaries will inform clinicians in the intervention group of high-risk results identified by the AI algorithm. Clinicians in the usual care group will not receive any communication from the study investigators regarding AI predictions.

Enrollment

1,000 estimated patients

Sex

All

Ages

40+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Atrial fibrillation algorithm

    1. Age 65 or over
    2. ECG obtained as part of routine clinical care
  2. Structural heart disease algorithm

    1. Age 40 or over
    2. ECG obtained as part of routine clinical care

Exclusion criteria

  1. Atrial fibrillation algorithm

    1. No history of AF
    2. No permanent pacemaker (PPM) or implantable cardioverter defibrillator (ICD)
    3. No recent cardiac surgery (within the preceding 30 days)
  2. Structural heart disease algorithm

    1. No history of SHD
    2. No echocardiogram within the past 1 year

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

1,000 participants in 2 patient groups

Intervention
Experimental group
Description:
Care teams randomized to the intervention will have access to the AI-enabled ECG-based screening tool.
Treatment:
Device: Risk-Based Assessment for Cardiac Dysfunction
Control
No Intervention group
Description:
Care teams randomized to control will continue routine practice without access to the AI-enabled ECG-based screening tool.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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