Implementing Individualized Patient Reported Outcome Measures in Routine Care of Patients With Coronary Artery Disease
Recruiting
N/A
Interventional Study
Coronary Artery Disease
Patient Acceptance of Health Care
Physician-Patient Relations
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 40 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 200 (estimated)
- Sponsor
- University of Calgary · Other
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About This Trial
Investigators recently developed the APPROACH electronic patient reported outcome (ePROM) Survey and Clinician Report tools to collect individual results from online quality of life and health status surveys for patients with coronary heart disease, and report them back to their treating clinicians. This pilot interventional study uses a pre-post design to assess whether implementing the ePROM sys…
Trial Locations
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Eligibility Criteria
Patient Inclusion Criteria:
* age at least 40 years.
* either (i) known coronary artery disease (defined as a history of myocardial infarction, percutaneous or surgical coronary revascularization, or documentation of obstructive coronary artery disease on previous invasive or CT angiography) or (ii…
Contacts