Patient-reported outcomes

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Abstract

In 2002, the National Institutes of Health (NIH) embarked upon a bold plan called "the NIH Roadmap" to identify and improve impediments to biomedical research in the twenty-first century. Three key areas were identified that would catalyze research discovery: New Pathways to Discovery, Research Teams of the Future, and Re-engineering the Clinical Research Enterprise. The plan to reengineer the clinical research enterprise included the establishment of a multicenter cooperative group referred to as the Patient-Reported Outcomes Measurement Information System (PROMIS). Originally, the PROMIS network included researchers from seven US academic centers. Over time, that number has expanded to include 15 centers.

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Hinchcliff, M., & Cella, D. (2012). Patient-reported outcomes. In Scleroderma: From Pathogenesis to Comprehensive Management (pp. 673–678). Springer US. https://doi.org/10.1007/978-1-4419-5774-0_56

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