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Prospective Longitudinal Evaluation of AI-ECG in a NEwly Diagnosed Heart Failure

Prospective Longitudinal Evaluation of AI-ECG in a NEwly Diagnosed Heart Failure

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05817136
Acronym
(PLANE-HF)
Enrollment
80
Registered
2023-04-18
Start date
2023-01-11
Completion date
2024-06-11
Last updated
2023-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Keywords

Heart failure, Remote monitoring, Machine learning

Brief summary

Background: Heart Failure (HF) is a condition in which the heart can no longer adequately pump blood around the body. The number of patients diagnosed with HF is increasing, consuming 4% of the NHS budget, and deadlier than most cancers. Most patients suffer from HF with reduced Ejection Fraction (HFrEF), where adequate treatment can improve quality of life and survival. Less than 50% of patients receive gold standard NHS guided medication and less than 20% receive appropriate monitoring (via echocardiography surveillance). This study looks at the use of a 'smart stethoscope' (Eko DUO), a stethoscope that uses information collected from the heart in the form of electrical (ECG) and sounds (phonocardiogram, PCG) waveforms, to predict the pumping function of the heart via artificial intelligence (AI-ECG). Aims: By using the smart stethoscope, this study evaluates whether the use of an easy-to-use home self-monitoring programme can: * Provide a solution for the current poor compliance of NHS echocardiogram surveillance programmes for people with newly diagnosed HF * Provide real-time assessment of heart function in response to medication changes * Improve the health economic and health outcomes of HF in the NHS Methods: 80 participants with newly diagnosed HFrEF, due to pre-existing heart disease and non-heart related causes, will be identified by the clinical team at Imperial College NHS Trust and obtain consent for the research team to approach them. All consented participants will receive a smart stethoscope and instructions for twice-weekly, 15-second self-examination for 3-months. Participants will also be invited for an additional echocardiogram at 6 weeks post-diagnosis, in addition to the routine, standard of care NHS echocardiogram surveillance for HF.

Interventions

DIAGNOSTIC_TESTEko DUO

Acquisition of a single-lead ECG via patients self-examine themselves twice a week for 12 months.

Sponsors

Imperial College London
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Age 18 years or above * Able to give informed consent * Newly diagnosed with HFrEF (i.e., LVEF below 40%) assessed by a consultant cardiologist within the past two weeks.

Exclusion criteria

* Any chest wound, skin pathology or other feature that would prohibit routine Eko DUO examination. * Participants who have been diagnosed with HF previously

Design outcomes

Primary

MeasureTime frameDescription
Descriptive analysis of trends and association of raw AI-ECG signals changes that correlate with HF progression.Up to 18 months1. AI-ECG signal changes with LV impairment. 2. AI-ECG signal changes with medication optimization. 3. AI-ECG signal changes with healthcare episodes.

Secondary

MeasureTime frameDescription
Sensitivity and specificity of AI-ECG to predict HF progressionUp to 18 months1. AI-ECG prediction of HF trajectory deterioration or improvement. 2. AI-ECG prediction of clinical congestive HF

Countries

United Kingdom

Contacts

Primary ContactAbdullah Alrumayh
a.alrumayh21@imperial.ac.uk+447412335336
Backup ContactNicholas Peters
n.peters@imperial.ac.uk+44 (0)20 7594 1880

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026