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 project developed and piloted Mobile Patient-Reported Outcomes for Value and Effectiveness, a bilingual mobile patient-reported outcomes system integrated into primary care for ethnically and culturally diverse adult patients with multiple chronic conditions. It proved feasible, acceptable, and effective in enhancing communication and decision-making, while revealing usability and implementation challenges to address for broader adoption.
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.
Working with the American College of Rheumatology, this research created a clinical learning network to increase the use of rheumatoid arthritis patient-reported outcomes (PROs), developed a natural language processing algorithm to abstract PRO measures from the Rheumatology Informatics System for Effectiveness registry, and planned for a toolkit to disseminate best practices in the implementation of PROs.
The research team built, implemented, and tested an application to visually display patient-reported outcomes scores for patients with rheumatoid arthritis during a clinical visit, with the goal of improving shared decision making, patient self-efficacy, and other health outcomes.
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 made a personal health record available to HIV-positive individuals at a safety net institution to see if medication adherence would improve.
This project developed and pilot tested a screening module and clinical decision support system for adolescents’ behavioral health.
