# Implementation of Machine Learning in Heart Failure Trials

**Authors:** Letizia Rosa Romano, Marta Scimeca Odorico, Antonio Curcio

PMC · DOI: 10.1007/s11897-026-00752-1 · 2026-03-28

## TL;DR

This paper explores how machine learning can improve heart failure clinical trials by enabling more adaptive and inclusive research methods.

## Contribution

The paper introduces how machine learning can overcome limitations in traditional heart failure trial designs through enhanced data integration and adaptive methodologies.

## Key findings

- Machine learning improves patient stratification and inclusion criteria in heart failure trials.
- ML enables adaptive trial designs and dynamic endpoint evaluation.
- Challenges remain in addressing bias and regulatory adaptation in ML-based trials.

## Abstract

Heart failure (HF) is a heterogeneous syndrome that challenges the design and interpretation of results from clinical trials. This review examines how machine learning (ML) can address methodological constraints of traditional trial models, such as rigid eligibility criteria, fixed endpoints, and limited external validity.

By integrating multimodal data from electronic health records, imaging, biomarkers, and wearables, ML enhances patient stratification, refines inclusion criteria, and improves prediction of mortality, HF hospitalization, and treatment response. It also enables adaptive trial designs, continuous monitoring, and dynamic endpoint evaluation. Despite these advances, challenges related to bias, interpretability, and regulatory adaptation persist.

ML complements rather than replacing conventional methodologies, and promotes more adaptive, inclusive, and patient-centered HF research. Responsible implementation—based on transparency, rigorous validation, and fairness—may redefine evidence generation and bridge clinical trials with real-world practice.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** SERPINA3 (serpin family A member 3) [NCBI Gene 12] {aka AACT, ACT, GIG24, GIG25}
- **Diseases:** cardiovascular death (MESH:D002318), HF (MESH:D006333), DL (MESH:C537113), fatigue (MESH:D005221), WD (MESH:D009471), valvular disease (MESH:D006349), LV dysfunction (MESH:D018487), sudden cardiac death (MESH:D016757), Heart Fail (MESH:D055111), EF (MESH:D054144), renal dysfunction (MESH:D007674), death (MESH:D003643), ML (MESH:D007859), hypotension (MESH:D007022)
- **Chemicals:** spironolactone (MESH:D013148), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13032980/full.md

---
Source: https://tomesphere.com/paper/PMC13032980