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This study will test the hypothesis that low-income, disadvantaged patients can provide high-quality patient-generated health data and patient-reported outcomes through commercial technologies, and that these data can be used to improve healthcare quality and delivery.
This project developed a natural language processing electronic health record search tool that automatically identifies and ranks relevant clinical information based on a patient’s presenting complaint within the emergency department setting.
This research developed and evaluated a mobile health application to improve screening, intervention, and referrals in the care of pregnant women.
This project developed a patient-centric tool called the Surgical Risk Preoperative Assessment System to estimate the risk of adverse operative outcomes.
This project developed, implemented, and assessed a patient data collection and clinician feedback system for depression care management in primary care practices, and found improvements in patient medication filling and adherence.
This project evaluated the usability of medication fulfillment data obtained from electronic health records and piloted a clinical decision support tool that alerted physicians to potential hypertensive medication adherence lapses.
A computer support system for clinical decisionmaking and tailoring patient education called HeartSmartKids™, has been developed to facilitate the translation of recommendations into practice. This current study will employ a comparative-effectiveness trial to evaluate clinician decision support and tailored patient education on the implementation of the current guidelines at school based health clinics.
This project evaluated whether the adoption of a community-wide health information exchange reduces utilization and costs of laboratory and radiology testing.
This project conducted an evaluation of the clinical outcomes, financial and economic impact, and patient and provider satisfaction of the WellMed Patient Centered Medical Home.
This project researched the perspectives of clinical and administrative leaders in small-to-medium sized ambulatory practices regarding their desired health information exchange functions, and barriers and facilitators of adoption.