Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05028686

Predicting Readmissions Using Omics, Biostatistical Evaluate and Artificial Intelligence

Status
Recruiting
Phase
Study type
Observational
Enrollment
500 (estimated)
Sponsor
Institute for Clinical Evaluative Sciences · Academic / Other
Sex
All
Age
18 Years – 105 Years
Healthy volunteers
Not accepted

Summary

This study is a prospective registry that aims to predict readmissions in patients with heart failure, using -omics, machine learning, patient reported outcomes, clinical data and other high-dimensional data sources.

Detailed description

There is substantial need to better predict outcomes across the spectrum of heart failure (HF) phenotypes in order to provide more efficient care with greater precision. Specifically, no validated methods have been adopted to predict outcomes reflecting transitions in health status across the continuum of HF and changes in cardiac function. A key transition is hospitalization - either readmission or de novo cardiovascular hospital admission. This is a major unmet health care need, to be able to better predict who will require hospital admission. Novel contributions of biomarkers, -omics, remote patient monitoring, and artificial intelligence (AI). It is anticipated that prediction of readmission and many other outcomes will be further improved by measurement of circulating biomarkers and by incorporating methods from AI including machine learning and probabilistic generative models that can incorporate the lens of how physicians and patients think. Machine learning that incorporates many different types of data, including physician interpretation and a broad array of biomarker/-omics molecular information can lead to significant improvements in predictive accuracy. Novel multimarker strategies coupled with machine learning may enable the ability of physicians to predict a range of outcomes (e.g., transitions in HF health status and LVEF) and refine clinical prediction models. Furthermore, the investigators will collect patient data, including patient reported outcome measures (PROMs), and physiological data (e.g. heart rate, blood pressure, and daily weights data) and integrate these data points into predictive models. The investigators will use the PROMs obtainable using Medly as a predictor of hospitalization, and as an outcome. In this proposal, the investigators will take advantage of recent advances in both deep and high throughput proteomics technologies to perform high-resolution analyses. These novel factors can be integrated into new electronic algorithms to improve HF care in the population.

Conditions

Interventions

TypeNameDescription
OTHERNo interventionObservational cohort

Timeline

Start date
2019-02-01
Primary completion
2024-09-30
Completion
2029-09-30
First posted
2021-08-31
Last updated
2021-09-02

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT05028686. Inclusion in this directory is not an endorsement.