Coronary Artery Disease Clinical Trial
Official title:
Cluster Randomized Trial of a Goal-Setting Intervention With Performance Feedback Reports Regarding Diabetes and Coronary Artery Disease for Family Physicians in Ontario
There remains a large gap between ideal and actual care provided to patients with chronic diseases. Performance feedback reports are often used as a foundation for quality improvement interventions. There have been hundreds of trials investigating the use of feedback reports; the important question to ask now is not whether performance feedback reports can help to improve quality of care, but how to optimize feedback interventions to accomplish that goal. The purpose of this study is to test whether a theory-based intervention added to feedback reports sent to primary care providers can result in improved outcomes for patients with chronic disease.
There remains a large gap between ideal and actual care provided to patients with chronic
diseases such as type-2 diabetes (DM2) and coronary artery disease (CAD), making them a
common focus for translational research. Quality improvement strategies such as audit and
feedback, which can increase adoption and adherence to guidelines, may be a good choice for
such problems. Audit and feedback is felt to be effective because it may overcome
physicians' limited ability to accurately self-assess. A recent Cochrane review concluded
that it may increase appropriate clinical practice by 5 to 10 percentage points. However,
the authors noted great variability in the results of the trials. It is thought that optimal
design and delivery of feedback will more consistently lead to improved results, but few
studies have tested different designs of feedback. A more recent meta-analysis of feedback
found that interventions incorporating theoretical principles from psychology in the design
were more effective than intuitive feedback designs. The author of that study has urged the
creation of more 'actionable' feedback. There is both theoretical and empirical reason to
believe that feedback will be more effective if the recipients set goals and develop action
plans.
A group of family physicians across Ontario have previously signed data sharing agreements
with ICES allowing their electronic medical records to be audited. These physicians will be
invited to participate in this trial. Participants will receive performance feedback reports
summarizing the percentage of their DM2 and CAD patients who are meeting evidence-based
targets for quality of care.
Participating physicians will be split into two groups at the level of their practice to
reduce risk of contamination. Minimization software will be used to ensure balance at
baseline in the primary outcomes between the intervention and control group. New potential
participants that have signed data sharing agreements at ICES will be invited to join the
trial for a maximum of six months after the first practices are allocated.
The intervention group will receive in addition to the feedback reports a theoretically
informed worksheet meant to facilitate goal-setting and the development of action plans.
This will occur every six months for two years. Outcomes will be analyzed after 24 months.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Health Services Research
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