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      Patient-Reported Outcomes Measurement Information System (PROMIS): efficient, standardized tools to measure self-reported health and quality of life.

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          Abstract

          All nurses are interested in the effects of diseases and treatments on individuals. Patient-reported outcome (PRO) measures are used to obtain self-reported information about symptoms, function, perceptions, and experiences. However, there are challenges to their use, including multiple measures of the same concept, widely varying quality, excessive length and complexity, and difficulty comparing findings across studies and conditions. To address these challenges, the National Institutes of Health funded the Patient-Reported Outcomes Measurement Information System (PROMIS), a web-based repository of valid and reliable PRO measures of health concepts relevant to clinician and researchers. Through the PROMIS Assessment Center, clinicians and researchers can access PRO measures, administer computerized adaptive tests, collect self-report data, and report instant health assessments. The purpose of this article was to summarize the development and validation of the PROMIS measures and to describe its current functionality as it relates to nursing science.

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          Author and article information

          Journal
          Nurs Outlook
          Nursing outlook
          Elsevier BV
          1528-3968
          0029-6554
          July 13 2014
          : 62
          : 5
          Affiliations
          [1 ] Nursing Research and Translational Science, Nursing Department, National Institutes of Health Clinical Center, Bethesda, MD. Electronic address: mbevans@cc.nih.gov.
          [2 ] Nursing Research and Translational Science, Nursing Department, NIH Clinical Center, Bethesda, MD.
          [3 ] Department of Medical Social Sciences, Feinberg School of Medicine, Northwestern University, Chicago, IL; Center for Patient-Centered Outcomes, Institute for Public Health and Medicine, Chicago, IL.
          Article
          S0029-6554(14)00106-7 NIHMS612484
          10.1016/j.outlook.2014.05.009
          4179871
          25015409
          81132652-f22d-4035-8985-b45b5c2ca363
          History

          Web-based data collection,Item response theory,Measurements,Patient-centered outcomes

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