RecruitingNot ApplicableNCT06164457

Implementing Individualized Patient Reported Outcome Measures in Routine Care of Patients With Coronary Artery Disease

Implementing Individualized Patient Reported Outcome Measures in Routine Care of Patients With Coronary Artery Disease: a Pilot Study


Sponsor

University of Calgary

Enrollment

200 participants

Start Date

Jun 8, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

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 system into routine care is feasible and acceptable to patients and physicians, and to inform feasibility for a larger clinical trial. Specifically, the investigators aim to evaluate use of the ePROM Patient Survey and Clinician Report among eligible outpatients with known or suspected coronary artery disease and their cardiologists. Additionally, the investigators aim to determine if the use of the APPROACH ePROMs Clinician Report in routine medical encounters is acceptable (based on administrative burden, ease of use, and time required) to patients and clinicians, and supports effective communication for management of symptoms of coronary artery disease.


Eligibility

Min Age: 40 Years

Inclusion Criteria5

  • 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) suspected coronary artery disease (defined as stable angina or anginal equivalent symptoms) as the reason for referral to a cardiologist.
  • Able to communicate in English or be willing to have an English-speaking family member or friend assist with survey completion.
  • Access to the internet, valid email address, and a web-enabled device, for survey completion.
  • Upcoming outpatient visit with a study cardiologist in the next 14-28 day

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Interventions

OTHERePROM Survey

The APPROACH ePROM survey consists of several well validated PROM instruments, including the Seattle Angina Questionnaire 7-item version,\[4\] the EuroQol EQ5D-5L,\[5\] the Medical Outcomes Study Social Support Scale (8 item version),\[6\] the Patient Health Questionnaire 2-item and 9-item (PHQ2/9) depression screening tools\[7\], and the Self-Care of Coronary Heart Disease Inventory (SC-CHDI-V3).\[8\]


Locations(2)

Cumming School of Medicine, University of Calgary

Calgary, Alberta, Canada

Department of Medicine, University of Alberta

Calgary, Alberta, Canada

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NCT06164457


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