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Recruiting Observational

Prediction of Heart-Failure with Machine Learning

NCT06819618 · tracked via the Priya Life Science Germany tracker
Phase
Observational
Started
2024-04-01
Last updated
2025-02-11

Condition(s) studied

Heart Failure with Reduced Ejection FractionHeart FailureHeart Failure,CongestiveHeart Failure AcuteHeart Failure; with Decompensation

Investigational drug(s) / intervention(s)

Monitoring with Apple Watch

Monitoring with Apple Watch: Patients will receive Apple Watch for Monitoring of Biosignals throughout the hospital stay

Study summary

In this monocentric observational study the research question is to what extent data collected via Apple Watch can predict the heart failure status of decompensated HF patients. For this purpose, physiological data from the Apple Watch (such as single-lead electrocardiogram, SpO2, respiratory rate, step count, nighttime temperature, etc.) will be extracted and used as predictor variables to forecast outcomes like risk of decompensation and rehospitalization within the follow-up period. Since this is a data-driven study, additional data collected as part of guideline-compliant treatment will also be included.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * age over 17 * HFrEF with LV-EF under 41 * hospitalized for decompensated heart failure with a) nTproBNP over 1000 AND b) willing to participate AND c) at least one out of three clinical signs (edema, pleural effusion, ascites) Exclusion Criteria: * life expectancy under 6 months due to non-cardiac conditions * inability to use smartwatch * severe valvular lesions

Primary outcome measure(s)

  • Re-hospitalization — 3 Months after discharge from hospital
    Re-hospitalization due to decompensated Heart Failure

Trial sites (1)

FacilityCityRegionStatus
University Medical Center Goettingen Goettigen Lower Saxony Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06819618 on ClinicalTrials.gov ↗ ← All trials in Germany