Education Catalog

SmartState: An Automated Research Protocol Adherence System Developing and enforcing study protocols is crucial in medical research, especially as interactions with participants become more intricate. Traditional rules-based systems struggle to provide the automation and flexibility required for real-time, personalized data collection. We introduce SmartState, a state-based system designed to act [...]

Real-World Computable Phenotypes of Patient-Reported Disability in Multiple Sclerosis Common tools to measure multiple sclerosis (MS) disability are rarely available in the real-world clinical setting. Leveraging electronic health records (EHR) data and disability outcomes from two independent EHR-linked MS research registries, we aimed to develop test and validate computable phenotypes [...]

The Evolve to Next-Gen Accrual to Clinical Trials (ENACT) (previously known as ACT) network was established in 2015 with funding from the NCATS. ENACT is a large federated network of EHR data repositories at 57 CTSA hubs that serves as an information superhighway for querying EHR data on >142M patients [...]

The National Institutes of Health All of Us Research Program has launched an innovative pilot to inform U.S. healthcare interoperability leaders in translational science on the use of health information exchanges (HIEs) and health information networks (HINs) in participant-consented research studies. The panel will share perspectives on the technical and [...]

Health Records to Improve Opioid Use Disorder Clinical Care The purpose of the panel is to discuss and inform the researchers and practitioners about the differences between task-specific models versus general-purpose models, namely, between Named Entity Recognition (NER) models and Large Language Models (LLM). NER is an important task in [...]