| Literature DB >> 26911821 |
Arlene E Chung1, Robert S Sandler2, Millie D Long2, Sean Ahrens3, Jessica L Burris4, Christopher F Martin5, Kristen Anton6, Amber Robb5, Thomas P Caruso7, Elizabeth L Jaeger5, Wenli Chen5, Marshall Clark5, Kelly Myers8, Angela Dobes9, Michael D Kappelman10.
Abstract
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.Entities:
Keywords: PGHD; patient engagement; patient-centered outcomes research; patient-reported outcomes; person-generated health data; wearables
Mesh:
Year: 2016 PMID: 26911821 PMCID: PMC4901381 DOI: 10.1093/jamia/ocv191
Source DB: PubMed Journal: J Am Med Inform Assoc ISSN: 1067-5027 Impact factor: 4.497