Harnessing person-generated health data to accelerate patient-centered outcomes research: the Crohn’s and Colitis Foundation of America PCORnet Patient Powered Research Network (CCFA Partners)
Author(s) -
Arlene E. Chung,
Robert S. Sandler,
Millie D. Long,
Sean Ahrens,
Jessica L. Burris,
Christopher F. Martin,
Kristen Anton,
Amber Robb,
Thomas P. Caruso,
Elizabeth Jaeger,
Wenli Chen,
Marshall Clark,
Kelly D. Myers,
Angela Dobes,
Michael D. Kappelman
Publication year - 2016
Publication title -
journal of the american medical informatics association
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.614
H-Index - 150
eISSN - 1527-974X
pISSN - 1067-5027
DOI - 10.1093/jamia/ocv191
Subject(s) - foundation (evidence) , translational research , patient centered outcomes , medicine , health care , outcomes research , public relations , knowledge management , business , alternative medicine , nursing , political science , computer science , pathology , law
The Crohn's and Colitis Foundation of America Partners Patient-Powered Research Network (PPRN) seeks to advance and accelerate comparative effectiveness and translational research in inflammatory bowel diseases (IBDs). Our IBD-focused PCORnet PPRN has been designed to overcome the major obstacles that have limited patient-centered outcomes research in IBD by providing the technical infrastructure, patient governance, and patient-driven functionality needed to: 1) identify, prioritize, and undertake a patient-centered research agenda through sharing person-generated health data; 2) develop and test patient and provider-focused tools that utilize individual patient data to improve health behaviors and inform health care decisions and, ultimately, outcomes; and 3) rapidly disseminate new knowledge to patients, enabling them to improve their health. The Crohn's and Colitis Foundation of America Partners PPRN has fostered the development of a community of citizen scientists in IBD; created a portal that will recruit, retain, and engage members and encourage partnerships with external scientists; and produced an efficient infrastructure for identifying, screening, and contacting network members for participation in research.
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