The investigators will perform a multi-site cluster randomized trial that uses a stepped-wedged design to compare the effectiveness of a Question Prompt List (QPL) intervention to usual care for patients considering high-risk vascular (peripheral, cardiac, neuro) and oncologic operations. This 24-month study will use a time-dependent cluster randomization plan within each of the five study sites: the investigators will randomly assign time points for surgeons who perform high risk operations to cross over from usual care to QPL intervention. Study staff will audiotape the conversation between the patient and surgeon during one preoperative clinic visit; administer surveys to patients and family members at 24 hours, 6 weeks and 12 weeks after that visit; and record surgical decisions, treatments received and associated outcomes. The investigators will use stratified purposeful sampling to identify a subset of patients in each study arm who have experienced serious complications for qualitative interviews.
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Patient Engagement in Decision Making Measured by Clinic Visit Transcript Coding for Number of and Types of Questions Raised
Timeframe: Within 2 hours of enrollment in the study
Change in Illness-related Stress Measured by Participant Self-report on MYCaW Instrument
Timeframe: 24-48 hours after enrollment, 6-8 weeks post-enrollment and 3-4 months post-enrollment
Perceived Self-efficacy in Patient-physician Interactions Measured by Participant Self-report on the PEPPI-5 Scale
Timeframe: 24-48 hours after enrollment
Post-treatment Regret Measured by a Specific Participant Self-report Survey Item
Timeframe: 3-4 months post-enrollment