AAAS has recieved a grant from the Agency for Healthcare Research and Quality  (AHRQ) to study an emerging source of health-related data – online patient generated health registries. The project will open up a new field of inquiry, examining such areas as how these registries are organized, their potential contributions to medical research, and related ethical and policy issues.
About the Project
The use of registries as an adjunct or alternative to randomized controlled trials in medical research, coinciding with the rapid growth of social networking, has produced a burgeoning phenomenon - online patient-generated health registries. The information in the registries is potential data for use by scientists in medical and behavioral research.
Using multiple search strategies the project will identify as many of these registries as possible; create a profile of each registry; characterize the registries on the basis of the data elements they contain; and describe how scientists have used the registries in their research. Data collected will cover such matters as privacy and data confidentiality, types of information submitted by patients, policies regarding access to patient information, and so on. The data from the registry profiles will be aggregated and a report prepared describing the project's findings and conclusions. Some of the data generated from this project will also be integrated with AHRQ's Registry of Patient Registries (RoPR) project.
This project is supported by grant number R03HS021371 from the Agency for Healthcare Research and Quality.