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This research will identify and characterize the factors differentiating patient portal users from non-users and develop guidelines to optimize portal design and development for population subgroups.
The goal of this project was to inform development of several Stage 3 Meaningful Use patient engagement objectives.
This project studied patient portals, their use in primary care, and the impact of use on chronic conditions, and identified opportunities to improve adoption of patient portals.
This project evaluated the impact of an inpatient portal used by cardiac patients and found that patients using the portal had a lower 30-day hospital readmission rate.
The goal of this project is to improve chronic illness care for ethnically and racially diverse patients using a patient portal.
Using a community-based participatory partnership, this project will delineate the factors that facilitate or limit the use of electronic personal health information management.
This project demonstrated the ability of an interoperable health information exchange and an electronic health record to provide useful quality and safety measures for the vulnerable populations served by two community health center clinics.
This project evaluated whether an interactive voice response system used by parents prior to routine health maintenance visits could improve parental activation, the comprehensiveness of care provided, and medication safety.
Develop a comprehensive plan for health IT implementation and integration by assessing specific clinical and organizational needs, feasibility of health IT implementation, defining project parameters, developing the implementation plan, and specifying procedures for ongoing evaluation and feedback.
Developed approaches to share data on patient clinical and diagnostic information across systems and created an implementation plan for systems integration.