USA, CA, San Francisco
This is a questionnaire designed to be completed by individuals with chronic care needs in patient homes. The tool includes questions to assess the current state of patient portals, the internet, and mobile devices.
This research will develop an information technology and implementation strategy for using patient-reported outcomes in primary care settings caring for diverse patients with multiple chronic conditions.
This project will use mobile health technology to collect patient-reported outcomes after dental procedures to optimize the quality of acute post-operative dental pain management.
This project will create and evaluate a learning network to expand the use of the Rheumatology Informatics System for Effectiveness (RISE) registry for patient-reported outcomes on rheumatoid arthritis.
This project will develop and evaluate an an electronic dashboard to display patient reported outcomes for patients with rheumatoid arthritis that will facilitate clinician and patient conversations about their care.
Informed by patients, caregivers, and an advisory panel of researchers and clinicians, this research developed, implemented, and evaluated an online patient portal tutorial for patients with chronic conditions.
This research created, piloted, and evaluated FIQS, the Family Input to Quality and Safety tool, that allows pediatric patients and their caregivers to provide safety reports regarding their inpatient care.
This project designed and pilot tested a dashboard that synthesizes patient data from a registry and found that it decreased the average monthly visit no-show rate.
The Self-Management Automated Real Time Telephone Support (SMART-Steps) provided surveillance, education, and telephone care management guided by questions on patient behavior.
Thirty-three states and 1 territory formed the HISPC, which aims to address the privacy and security challenges presented by electronic health information exchange through multi-state collaboration.