This is a single-center, double-arm, open-label, randomized feasibility study that will determine whether a novel clinical decision aid accessed via the electronic health record will be acceptable to both cancer survivors and their cardiologists, will favorably impact appropriate medication use and cardiac imaging surveillance, and will improve clinician and patient decision-making, perception, and behavior towards cardioprotective medication usage and cardiovascular disease imaging utilization.
For this feasibility study, the researchers will create the clinical decision aid and test the central hypothesis that this novel clinical decision aid accessed via the electronic health record will be acceptable to both cancer survivors and their cardiologists and will favorably impact appropriate medication use and cardiac imaging surveillance. The hypothesis is supported by preliminary data suggesting that an initial and rudimentary version of the clinical aid increases appropriate medication use and imaging follow-up in cardio-oncology patients. Success will be determined by ≥85% of clinic visits using the clinical decision aid resulting in pursuit of medication use and cardiac imaging surveillance patterns commensurate with recommendations specific to cancer survivors, with overall rates the same or higher than the group without the clinical decision aid, as well as overall favorable patient and physician focus group comments and survey responses.
Study Type
OBSERVATIONAL
Enrollment
60
The clinical decision aid tool will be used at the subject's first visit (Week 0), Week 12 and Week 24.
Cardiology clinic visits will take place at the subjects first visit (Week 0), Week 12 and Week 24.
Froedtert & the Medical College of Wisconsin
Milwaukee, Wisconsin, United States
Medication use
The number of subjects in which medication use pursued is consistent with current medical society recommendations appropriate for the subject.
Time frame: Week 0
Medication use
The number of subjects in which medication use pursued is consistent with current medical society recommendations appropriate for the subject.
Time frame: Week 12
Medication use
The number of subjects in which medication use pursued is consistent with current medical society recommendations appropriate for the subject.
Time frame: Week 24
Imaging surveillance
The number of subjects in which imaging surveillance pursued is consistent with current medical society recommendations appropriate for the subject.
Time frame: Week 0
Imaging surveillance
The number of subjects in which imaging surveillance pursued is consistent with current medical society recommendations appropriate for the subject.
Time frame: Week 12
Imaging surveillance
The number of subjects in which imaging surveillance pursued is consistent with current medical society recommendations appropriate for the subject.
Time frame: Week 24
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