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 study implemented a mobile health (mHealth) platform to measure patient-reported outcomes for pain management after certain dental procedures to determine the impact on the patient pain experience.
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.
This project examined the fidelity of the implementation of the Self-Management Automated Real-Time Telephone Support program to better-inform tailoring of health
This project made a personal health record available to HIV-positive individuals at a safety net institution to see if medication adherence would improve.
