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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 project will implement and evaluate a previously developed, interactive, patient-centered discharge toolkit to improve the transition of care from the inpatient to outpatient settings.
This project developed, implemented, and evaluated a program that includes clinical decision support to improve diagnosis of hypertension in children.
This project integrated a validated anxiety-specific screening tool in an existing clinical decision support system and tested it with a randomized feasibility pilot that found the tool did not increase detection of anxiety in pediatric primary care.
This project evaluated the effects of providing caregivers of older adults proxy access to electronic patient portals and found that information exchange between caregivers and providers increased.
This project identified patients’ needs, preferences, and responses when receiving abnormal test result notifications through an electronic patient portal, and developed a usable prototype to improving test result communication.
This project developed a tool to promote activation, communication, engagement, and self-management of pediatric blood and marrow transplant patients and their parents and found that patient-centric tools can successfully engage caregivers in hospital care.
This project evaluated the use of an asthma portal by focusing on provider implementation and health outcomes for children, low-income families, and children with special health care needs.
The goal of this project was to inform development of several Stage 3 Meaningful Use patient engagement objectives.
This research studied the healthcare information needs of elders and their family caregivers and developed an online platform to allow this group to share health information.