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OpenTrials
Completed

NCT Number: NCT02272062

Patient-Reported Preferences Affecting Revascularization Decisions

Selection of a treatment strategy for patients with symptoms due to coronary artery disease requires consideration of patient preferences. In current clinical practice, patient preferences for treatment may not be known prior to diagnostic coronary angiography. The investigators will test an internet-based shared decision-making tool which will provide education and solicit preference information prior to angiography. The investigators seek to determine if this tool can accurately assess patient preferences, and if these preferences will lead to a change in clinical management.

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Key information

About this study

Selecting a treatment strategy for patients with symptomatic coronary artery disease (CAD) requires integrated consideration of symptom burden, patient preferences, and practice guidelines. In many clinical scenarios, there is equipoise regarding the need to revascularize (percutaneous coronary intervention (PCI) vs. medical management) and/or the type of revascularization (PCI vs. bypass surgery). Patients may have minimal direct input in the decision to proceed to a revascularization procedure, especially in the case of ad hoc PCI.

There is little guidance in the literature regarding strategies to improve patient participation in revascularization decisions. There is no shared decision-making tool to provide accessible information to the interventional cardiologist prior to PCI. An educational program that provides basic information regarding CAD and revascularization procedures could lead to improved patient knowledge and informed participation in these critical decisions. A clinical survey that assesses patient symptom burden and preferences could provide valuable information to physicians at the time of angiography. The investigators aim to test a clinical tool that addresses both of these needs and can be administered in the pre-procedure area immediately prior to angiography. If successful, this tool could lead to greater informed patient participation in revascularization procedures and improved patient satisfaction.

First, the investigators will conduct a pre-post analysis. The first 100 enrolled patients will undergo usual care without the use of the decision-making tool. Surveys prior to angiography and at 3 months will test knowledge and decisional self-efficacy. Subsequently, 200 patients will utilize the decision-making tool and will complete the same surveys. Comparison of these groups will test the ability of the decision-making tool to improve knowledge about CAD and accurately assess preferences.

Among the 200 patients utilizing the decision-making tool, patients will be randomly assigned to have, or not have, their preferences shared with the interventional cardiologist at the time of catheterization. This randomized portion of the study will test the impact of patient preferences on treatment decisions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients referred to the catheterization laboratory for diagnostic coronary angiography with a reasonable expectation of coronary artery disease, defined as chronic stable angina, chest pain with a positive functional study, unstable angina, or non-ST segment elevation myocardial infarction.

Exclusion criteria

  • Unable to provide informed consent
  • Unable to speak or read English
  • Critical illness
  • When a delay in angiography to administer the decision aid could lead to adverse clinical outcome

Treatment and study plan

Decision-making tool for coronary artery disease treatment

Other

A brief internet-based tool will provide education about coronary artery disease and assess patient preferences regarding treatment options (medical management, percutaneous coronary intervention, or coronary artery bypass graft). This information will be provided to the treating interventional cardiologist at the time of coronary angiography in the treatment group.

Primary outcomes

  1. Concordance of patient preference with delivered treatment

    Time frame: 3 months

    Among patients with significant coronary artery disease on diagnostic angiography, the percentage of subjects with delivered therapy (medical management, percutaneous coronary intervention, coronary artery bypass graft) identical to preferences expressed prior to angiography.

Secondary outcomes

  1. Knowledge

    Time frame: Within 2 hours of angiography

    Performance on a 6-item knowledge questionnaire

  2. Knowledge

    Time frame: 3 months

    Performance on a 6-item knowledge questionnaire

  3. Decisional conflict

    Time frame: Within 2 hours of angiography

    Performance on a 16-item scale assessing decisional self-efficacy

  4. Patient satisfaction

    Time frame: Within 2 hours of angiography

    Performance on the decisional regret scale

  5. Patient satisfaction

    Time frame: 3 months

    Performance on the decisional regret scale

  6. Informed values congruence

    Time frame: Within 2 hours of angiography

    Concordance of the subject's stated preference for treatment with treatment-specific results from the Patient Preferences Questionnaire for Angina Treatment

  7. Angina

    Time frame: 3 months

    7-item Seattle Angina Questionnaire

  8. Ad hoc percutaneous coronary intervention

    Time frame: 3 months

    Percentage of percutaneous coronary intervention performed at time of diagnostic angiography

Sponsors and collaborators

Lead sponsor

Duke University

Other

Collaborators

  • Gilead Sciences

Registry information

Acronym: PREPARED

Important dates

Study start
2014
Primary completion
2016
Study completion
2016
First posted
Oct 22, 2014
Registry last updated
Aug 3, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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