Technical Data Health Care Systems Core
Core Activities
The Technical Data and Health Care Systems Core provides the opportunity, conceptual foundations, technical expertise, and research resources for investigators and health care system to partner to design and conduct rigorous, feasible and highly impactful ePCTs of non-pharmacological interventions to improve dementia care.
The Core builds relationships with health care systems in variety of settings willing to host these trials and identifies priority areas for dementia care in these settings. Through the Project Planning Grants program, the Core fosters partnerships between investigators and HCS to enable the development of rigorous ePCT protocols to address those priority areas. The Core also enables the application of electronic health records and other real world data structures to conduct ePCTs. The Core helps build investigator capacity through IMPACT’s various training opportunities and develops and disseminates knowledge to advance best practices and methodologies in the design and conduct of ePCTs in dementia specifically related to use of data platforms and health care system organization.
Key Resources
News & Publications
- IMPACT researchers explore approaches to dementia caregiver identification and recruitment
- IMPACT scholar appointed editor of Palliative Medicine Report
- IMPACT member leads hospice/palliative care survey in NY State to inform nursing school education
- IMPACT physicians contribute to Health Affairs article addressing costs of dementia care
- JAMDA article describes innovation of the LTC Data Cooperative
- IMPACT members find critical barriers among care partners and older adults with cognitive impairment during emergency department care transitions
- Travers, Gifford and Baier co-author qualitative study on providers’ perspectives on high-quality dementia care
Leadership
![]() Dae Hyun Kim, MD, MPH, ScD Core Leader |
![]() Daniella Meeker, PhD Associate Core Leader |
Health Care System Scholars Program
One-year support for junior and senior investigators to work directly with health care systems interested in improving care provided to people living with AD/ADRD and their care partners. RFAs are generally released in January of each year.



