General Internal Medicine

Aggregates data from various UF Health clinical and administrative information systems, including Epic. Designed to provide a count of the unique patients by diagnoses, treatments, and demographics. This can be a useful tool for study planning, grant proposals, IRB protocols, and similar research activities.

Data and stats by health topic; includes interactive charts and tools, state data, etc.

From the Agency for Healthcare Research and Quality (AHRQ). Includes Healthcare Cost and Utilization Project (HCUP), Medical Expenditure Panel Survey (MEPS), State Snapshots, US Health Information Knowledgebase (USHIK). Permissions needed to access some data.

From the CDC. Includes National Health & Nutrition Examination Survey, National Health Care Surveys, National Vital Statistics System, etc.

A registry and results database of clinical studies of human participants; from the National Institutes of Health.

Data archive of the Robert Wood Johnson Foundation; some permissions needed to download data.

Global catalog of surveys, censuses, vital statistics, and other health-related data. From the Institute for Health Metrics and Evaluation at the University of Washington.

A curated general-purpose repository that makes the data underlying scientific publications discoverable, freely reusable, and citable.

Consumer Assessment of Healthcare Providers and Systems (CAHPS) surveys ask consumers and patients to report on and evaluate their experiences with health care.

HaPI is a database that provides access to information on approximately 15,000 measurement instruments. If accessing from off-campus, you will need to be logged in via the library proxy or VPN.

Select "Assessment" Resource Type for surveys ACIC (Assessment of Chronic Illness Care), PCMH-A (Patient-Centered Medical Home Assessment), and PACIC (Patient Assessment of Chronic Illness Care).

Q-Bank provides researchers and survey practitioners access to survey questions from federal agencies and question evaluation reports. Agencies include the National Center for Health Statistics, US Census Bureau, Bureau of Labor Statistics, National Cancer Institute, and National Science Foundation.

NIH encourages the use of common data elements (CDEs) in clinical research, patient registries, and other human subject research in order to improve data quality and opportunities for comparison and combination of data from multiple studies and with electronic health records.

Including information about tools for data management planning, data and file sharing, metadata and data standards, and data storage.

Create ready-to-use data management plans for specific funding agencies. Use your gatorlink and password to login.

Includes NIH-supported domain-specific repositories (open and limited access) and generalist repositories

A list of research data repositories, searchable by subject area.