IntuitionComparison of Physician Intuition and Model Predicted Prognosis in Heart Failure
This observational study compares the accuracy of physician's intuition and model predicted prognosis in heart failure, by looking at outcomes such as heart transplant, left ventricular assist device implant, and all-cause mortality within 1 year of study enrolment.
Data Collection
Collected from today forward - ProspectiveCardiovascular Diseases
+ Heart Diseases
+ Heart Failure
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: May 18, 2018
Actual date on which the first participant was enrolled.Heart failure (HF) is a significant medical issue affecting over 26 million people worldwide. The study aims to improve HF management by accurately assessing patient prognosis. Currently, doctors rely on their intuition to estimate survival rates, but predictive models have shown to be more accurate. This Canadian study compares physician intuition and model-predicted survival in ambulatory HF patients. By evaluating which method provides more accurate prognostic estimates, the study can inform the best strategy for patient management, offering greater clinical benefits and improving resource utilization. In this study, adult HF patients from various clinics across Canada will participate. Doctors with different levels of expertise will provide their intuitive estimates of a patient's one-year survival without knowing the model-predicted survival. The study will compare the accuracy of physician-predicted and model-predicted survival to the true one-year survival. It will also assess the impact of physician confidence, expertise, and gender, as well as patient gender, on the accuracy of physician intuition. The study will evaluate the association between physician-estimated survival and resource use, as well as related costs. Participants will be followed for a minimum of one year, and outcomes such as death, urgent heart transplant, and resource utilization will be collected.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.1400 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location