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The goal of this project is to generate a systematic and replicable process for transforming evidence-based research findings, including findings from patient-centered outcomes research, into shareable clinical decision support (CDS) standards and a publicly available CDS prototype.
This study showed that there is a range of how people communicate with their social network, how this information is communicated, the types of health information communicated, and the rationales for the communication.
This project created individualized, culturally and linguistically inclusive education materials for older adults from diverse backgrounds tailored to electronic medication information.
Developed approaches to share data on patient clinical and diagnostic information across systems and created an implementation plan for systems integration.