Suspended

IntuitionComparison of Physician Intuition and Model Predicted Prognosis in Heart Failure

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
Study Aim

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.

What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Cardiovascular Diseases

+ Heart Diseases

+ Heart Failure

Over 18 Years
+6 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: May 2018
See protocol details

Summary

Principal SponsorUniversity Health Network, Toronto
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitlePhysician Intuition Versus Model Predicted Prognosis in Heart Failure
Principal SponsorUniversity Health Network, Toronto
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

1400 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

Cardiovascular DiseasesHeart DiseasesHeart Failure

Criteria

3 inclusion criteria required to participate
Ambulatory HF patients followed in a HF clinic

Adults (>18 years)

Have a left ventricular ejection fraction (LVEF) ≤40% by echocardiogram

3 exclusion criteria prevent from participating
HF patients with preserved LVEF (>40%)

HF patients already on ventricular assist device support

Patients with acutely decompensated HF at the time of the clinic visit requiring admission or with a HF admission in the previous month to the index clinic visit.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

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

Suspended

University Health Network

Toronto, CanadaOpen University Health Network in Google Maps
SuspendedOne Study Center