Patient-reported outcomes

Monique Hinchcliff; David Cella

doi:10.1007/978-1-4419-5774-0_56

Patient-reported outcomes

Monique Hinchcliff^*, David Cella

^*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceeding › Chapter

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 language	English (US)
Title of host publication	Scleroderma
Subtitle of host publication	From Pathogenesis to Comprehensive Management
Publisher	Springer US
Pages	673-678
Number of pages	6
ISBN (Electronic)	9781441957740
ISBN (Print)	9781441957733
DOIs	https://doi.org/10.1007/978-1-4419-5774-0_56
State	Published - Jan 1 2012

Keywords

Behavior
Cognition
Disability
Functional limitation
Impairment
Mental
Physical
Social
Symptom

ASJC Scopus subject areas

General Medicine

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10.1007/978-1-4419-5774-0_56

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AB - 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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KW - Disability

KW - Functional limitation

KW - Impairment

KW - Mental

KW - Physical

KW - Social

KW - Symptom

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Patient-reported outcomes

Abstract

Keywords

ASJC Scopus subject areas

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