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| Volume
66 Number 3
May 1999 |
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| Quality of Life as a Construct in Health and Disability Research | 160 - 169 |
Margaret Brown, Ph.D.1, and Wayne A. Gordon, Ph.D.2 |
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| 1Consultant and 2Professor and Associate Director,
Department
of Rehabilitation Medicine, Mount Sinai School of Medicine, New York, NY.
Address correspondence to Wayne A. Gordon, Ph.D., Associate Director, Department of Rehabilitation Medicine, Box 1240, The Mount Sinai School of Medicine, One East 100th Street, New York, NY 10029 or address e-mail to: msjourn@doc.mssm.edu |
ABSTRACT
Definitional issues that affect the measurement of quality of life
(QOL) in health care research are discussed. In reviewing a broad
sample of health- and disability-related QOL studies, the authors note
several characteristics in which respective approaches to measurement differ:
(a) In various measurement tools, QOL has been located either within the
insider's (i.e., the person being measured) judgment of the 'goodness'
of his or her life or outside this judgment. (b) The insider's and/or
outsider's values may hold sway in deciding the elements of life that are
relevant to QOL within the measurement process, and in rating the degree
of 'goodness' of these life domains. (c) QOL models incorporate domains
of items varying in breadth and specificity; and they take either a negative
or neutral view of functioning. (d) QOL models vary in their complexity,
type of linkage between components, and inclusion (or not) of both the
insider's judgment and external predictors of QOL. These distinctions
are used by the authors in recommending approaches to QOL measurement suitable
for health care research aimed at outcome assessment and description of
populations.
KEY WORDS
Quality
of life, disability,
chronic
illness, research
methodology
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