Patient-reported outcomes

Monique Hinchcliff*, David Cella

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapter

2 Scopus citations

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.

Original languageEnglish (US)
Title of host publicationScleroderma
Subtitle of host publicationFrom Pathogenesis to Comprehensive Management
PublisherSpringer US
Pages673-678
Number of pages6
ISBN (Electronic)9781441957740
ISBN (Print)9781441957733
DOIs
StatePublished - Jan 1 2012

Keywords

  • Behavior
  • Cognition
  • Disability
  • Functional limitation
  • Impairment
  • Mental
  • Physical
  • Social
  • Symptom

ASJC Scopus subject areas

  • Medicine(all)

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  • Cite this

    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