search
Back to results

Triple Cardiovascular Disease Detection With an Artificial Intelligence-enabled Stethoscope (TRICORDER)

Primary Purpose

Heart Failure, Heart Valve Diseases, Atrial Fibrillation

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
AI-stethoscope
Sponsored by
Imperial College London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Heart Failure focused on measuring cluster randomized controlled trial, artificial intelligence, digital health, cardiology, primary care

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Primary care practices that care for adult patients and have the ability to request natriuretic peptide blood testing Primary care practices within the NIHR North West London Clinical Research Network or Betsi Cadwaladr University Health Board. Exclusion Criteria: Poor WiFi and/or mobile data connectivity within primary care consulting rooms No face-to-face patient consultations

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Intervention

    Control

    Arm Description

    Receive 3-6 AI-stethoscopes (Eko DUO, Eko Health Inc, CA, USA) including artificial intelligence software for detection of: Reduced left ventricular ejection fraction <40% Atrial fibrillation Cardiac murmurs

    Usual care

    Outcomes

    Primary Outcome Measures

    Incidence of heart failure (co-primary)
    Difference in incidence of coded new diagnoses of heart failure (HF)
    Ratio of route to diagnosis of heart failure (co-primary) between emergency and community-based pathways
    Difference in ratio of the incidence of coded diagnoses of HF via hospital admission-based versus community-based pathways.

    Secondary Outcome Measures

    Incidence of atrial fibrillation
    New coded diagnoses of atrial fibrillation (AF)
    Incidence of valvular heart disease
    New coded diagnoses of valvular heart disease (VHD)
    Cost-consequence (AF)
    Cost-consequence analysis (form of health economic evaluation) for diagnosis of atrial fibrillation, stratified by route to diagnosis. Presented in pounds sterling.
    Cost-consequence (HFrEF)
    Cost-consequence analysis (form of health economic evaluation) for diagnosis of HFrEF, stratified by route to diagnosis. Presented in pounds sterling.
    Cost-consequence (VHD)
    Cost-consequence analysis (form of health economic evaluation) for diagnosis of VHD, stratified by route to diagnosis. Presented in pounds sterling.
    Health service utilisation
    Health service utilisation for diagnostics e.g. rates of request for echocardiography, electrocardiography, primary care appointments. Collected from NHS organisation business intelligence repositories and UK Trusted Research Environments.
    Proportion of patients prescribed guideline-directed medical therapy
    Proportion of patients prescribedguideline-directed medical therapy (HF, AF, VHD)
    Device therapy
    New implantation of cardiac resynchronisation therapy (CRT) and/or implantable cardioverter-defibrillator (ICD)
    Uptake and utilisation
    Differential rates of uptake and utilisation of AI-stethoscope in primary care
    Determinants of uptake and utilisation
    Determinants of utilisation of AI-stethoscope in primary care (clinician questionnaires)
    Patient quality of life
    Healthy Days at Home (patient-level analysis)

    Full Information

    First Posted
    July 21, 2023
    Last Updated
    August 21, 2023
    Sponsor
    Imperial College London
    Collaborators
    Imperial College Health Partners
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT05987670
    Brief Title
    Triple Cardiovascular Disease Detection With an Artificial Intelligence-enabled Stethoscope
    Acronym
    TRICORDER
    Official Title
    Triple Cardiovascular Disease Detection With an Artificial Intelligence-enabled Stethoscope
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    October 1, 2023 (Anticipated)
    Primary Completion Date
    April 1, 2025 (Anticipated)
    Study Completion Date
    October 1, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Imperial College London
    Collaborators
    Imperial College Health Partners

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    Yes
    Product Manufactured in and Exported from the U.S.
    Yes
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Heart failure (HF) is a condition in which the heart cannot pump blood adequately. It is increasingly common, consumes 4% of the UK National Health Service (NHS) budget and is deadlier than most cancers. Early diagnosis and treatment of HF improves quality of life and survival. Unacceptably, 80% of patients have their HF diagnosed only when very unwell, requiring an emergency hospital admission, with worse survival and higher treatment costs to the NHS. This is largely because General Practitioners (GPs) have no easy-to-use tools to check for suspected HF, with patients having to rely on a long and rarely completed diagnostic pathway involving blood tests and hospital assessment. The investigators have previously demonstrated that an artificial intelligence-enabled stethoscope (AI-stethoscope) can detect HF in 15 seconds with 92% accuracy (regardless of age, gender or ethnicity) - even before patients develop symptoms. While the GP uses the stethoscope, it records the heart sounds and electrical activity, and uses inbuilt artificial intelligence to detect HF. The goal of this clinical trial is to determine the clinical and cost-effectiveness of providing primary care teams with the AI-stethoscope for the detection of heart failure. The main questions it aims to answer are if provision of the AI-stethoscope: Increases overall detection of heart failure Reduces the proportion of patients being diagnosed with heart failure following an emergency hospital admission Reduces healthcare system costs 200 primary care practices across North West London and North Wales, UK, will be recruited to a cluster randomised controlled trial, meaning half of the primary care practices will be randomly assigned to have AI-stethoscopes for use in direct clinical care, and half will not. Researchers will compare clinical and cost outcomes between the groups.
    Detailed Description
    Triple Cardiovascular Disease Detection with Artificial Intelligence-enabled Stethoscope (TRICORDER) is an open label, cluster randomised controlled trial. The aim is to determine whether use of an artificial intelligence-enabled stethoscope (AI-stethoscope) in UK Primary Care improves community-based detection of heart failure (HF), compared with usual care. 200 primary care practices in North West London and North Wales (UK) will be randomised to receive the AI-stethoscope (intervention arm) or continue with usual care (control arm). The intervention arm will use the AI-stethoscope in routine clinical practice. Outcomes will be measured using pooled primary and secondary care clinical and cost-data, as well as clinician questionnaires.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Heart Failure, Heart Valve Diseases, Atrial Fibrillation, Heart Murmurs, Congestive Heart Failure, Heart Failure With Reduced Ejection Fraction
    Keywords
    cluster randomized controlled trial, artificial intelligence, digital health, cardiology, primary care

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Open label cluster randomised controlled trial
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    200 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention
    Arm Type
    Experimental
    Arm Description
    Receive 3-6 AI-stethoscopes (Eko DUO, Eko Health Inc, CA, USA) including artificial intelligence software for detection of: Reduced left ventricular ejection fraction <40% Atrial fibrillation Cardiac murmurs
    Arm Title
    Control
    Arm Type
    No Intervention
    Arm Description
    Usual care
    Intervention Type
    Device
    Intervention Name(s)
    AI-stethoscope
    Other Intervention Name(s)
    Eko DUO, Eko Core 500, Eko EAS
    Intervention Description
    Clinicians at practices in the intervention arm will be provided with one session of in-person training in use of the AI-stethoscope within 2 weeks of randomisation, including Delivery and setup Smartphone app installation and login Pairing of all clinician smartphones with all AI-stethoscopes in the same practice Demo of patient examination The AI-stethoscope will be used within its CE/UKCA-marked intended purpose. The clinical guidelines for use have been agreed by the NHS North West London Integrated Care System and Betsi Cadwaladr University Health Board Cardiovascular Executive Groups. Patients will be examined with the AI-stethoscope in accordance with these guidelines, and/or where stethoscope examination is deemed clinically appropriate. Patients will provide verbal consent for examination with the AI-stethoscope as per any physical examination performed by healthcare professionals for direct care, in accordance with UK law and General Medical Council guidelines.
    Primary Outcome Measure Information:
    Title
    Incidence of heart failure (co-primary)
    Description
    Difference in incidence of coded new diagnoses of heart failure (HF)
    Time Frame
    24 months
    Title
    Ratio of route to diagnosis of heart failure (co-primary) between emergency and community-based pathways
    Description
    Difference in ratio of the incidence of coded diagnoses of HF via hospital admission-based versus community-based pathways.
    Time Frame
    24 months
    Secondary Outcome Measure Information:
    Title
    Incidence of atrial fibrillation
    Description
    New coded diagnoses of atrial fibrillation (AF)
    Time Frame
    24 months
    Title
    Incidence of valvular heart disease
    Description
    New coded diagnoses of valvular heart disease (VHD)
    Time Frame
    24 months
    Title
    Cost-consequence (AF)
    Description
    Cost-consequence analysis (form of health economic evaluation) for diagnosis of atrial fibrillation, stratified by route to diagnosis. Presented in pounds sterling.
    Time Frame
    24 months
    Title
    Cost-consequence (HFrEF)
    Description
    Cost-consequence analysis (form of health economic evaluation) for diagnosis of HFrEF, stratified by route to diagnosis. Presented in pounds sterling.
    Time Frame
    24 months
    Title
    Cost-consequence (VHD)
    Description
    Cost-consequence analysis (form of health economic evaluation) for diagnosis of VHD, stratified by route to diagnosis. Presented in pounds sterling.
    Time Frame
    24 months
    Title
    Health service utilisation
    Description
    Health service utilisation for diagnostics e.g. rates of request for echocardiography, electrocardiography, primary care appointments. Collected from NHS organisation business intelligence repositories and UK Trusted Research Environments.
    Time Frame
    24 months
    Title
    Proportion of patients prescribed guideline-directed medical therapy
    Description
    Proportion of patients prescribedguideline-directed medical therapy (HF, AF, VHD)
    Time Frame
    24 months
    Title
    Device therapy
    Description
    New implantation of cardiac resynchronisation therapy (CRT) and/or implantable cardioverter-defibrillator (ICD)
    Time Frame
    24 months
    Title
    Uptake and utilisation
    Description
    Differential rates of uptake and utilisation of AI-stethoscope in primary care
    Time Frame
    24 months
    Title
    Determinants of uptake and utilisation
    Description
    Determinants of utilisation of AI-stethoscope in primary care (clinician questionnaires)
    Time Frame
    24 months
    Title
    Patient quality of life
    Description
    Healthy Days at Home (patient-level analysis)
    Time Frame
    24 months
    Other Pre-specified Outcome Measures:
    Title
    Sensitivity analysis
    Description
    Patient-level sensitivity analyses will be performed for patients with abnormal Eko DUO predictions for HF, to identify direct associations between AI-stethoscope predictions and specific diagnostic codes for HF, AF and VHD
    Time Frame
    24 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Primary care practices that care for adult patients and have the ability to request natriuretic peptide blood testing Primary care practices within the NIHR North West London Clinical Research Network or Betsi Cadwaladr University Health Board. Exclusion Criteria: Poor WiFi and/or mobile data connectivity within primary care consulting rooms No face-to-face patient consultations
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Mihir Kelshiker, MD
    Phone
    020 7589 5111
    Email
    mihir.kelshiker10@imperial.ac.uk
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Nicholas S Peters, MD
    Organizational Affiliation
    Imperial College London
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    34998740
    Citation
    Bachtiger P, Petri CF, Scott FE, Ri Park S, Kelshiker MA, Sahemey HK, Dumea B, Alquero R, Padam PS, Hatrick IR, Ali A, Ribeiro M, Cheung WS, Bual N, Rana B, Shun-Shin M, Kramer DB, Fragoyannis A, Keene D, Plymen CM, Peters NS. Point-of-care screening for heart failure with reduced ejection fraction using artificial intelligence during ECG-enabled stethoscope examination in London, UK: a prospective, observational, multicentre study. Lancet Digit Health. 2022 Feb;4(2):e117-e125. doi: 10.1016/S2589-7500(21)00256-9. Epub 2022 Jan 5.
    Results Reference
    background
    PubMed Identifier
    36921978
    Citation
    Bachtiger P, Kelshiker MA, Petri CF, Gandhi M, Shah M, Kamalati T, Khan SA, Hooper G, Stephens J, Alrumayh A, Barton C, Kramer DB, Plymen CM, Peters NS. Survival and health economic outcomes in heart failure diagnosed at hospital admission versus community settings: a propensity-matched analysis. BMJ Health Care Inform. 2023 Mar;30(1):e100718. doi: 10.1136/bmjhci-2022-100718.
    Results Reference
    background

    Learn more about this trial

    Triple Cardiovascular Disease Detection With an Artificial Intelligence-enabled Stethoscope

    We'll reach out to this number within 24 hrs