Awardee OrganizationUNIVERSITY OF CALIFORNIA, SAN DIEGO
Description
Abstract Text
The Quality of Well-being Scale is an interviewer-administrated
measure of health-related quality of life. The measure has been used
in a wide variety of outcome and public policy studies. A major
feature of the measure is that it can be used for cost-utility analysis.
There have been at least three criticism of the QWB for outcome
studies in arthritis. First, the QWB must be administered by an
interviewer. Second, the QWB has not been validated specifically
for patients with arthritis. Third, the preference weighting system is
based on the general population rather than arthritis patients. The
QWB has recently been redeveloped as a self-administered
questionnaire (QWB-SA). The purpose of the study is to validate the
QWB-SA for patients with arthritis and musculoskeletal disorders.
This study has four Specific Aims. The first Aim is to demonstrate
the feasibility of the QWB-SA for patients with arthritis and
musculoskeletal disorders. The QWB-SA will be administered along
with the AIMS-2 and the SF-36 to 1,500 patients. Analysis will
consider rates of completed responses, difference in response, and
missing information. The second Specific Aim is to develop an
arthritis-specific QWB-SA. This will be accomplished by analyzing
data collected in relation to Specific Aim 1. Comparisons between
arthritis and non patients, using item analysis, will identify
components of the measure that separate arthritis patients from
patients with other illnesses. The third Aim is to compare
preferences from arthritis patients and non patients. This will be
accomplished by obtaining ratings for case descriptions and analyzing
whether patients have different preference for outcome that non
patients. The fourth Specific Aim will be to determine whether
patients have different preference for outcome when in acute or non
acute pain states. This study will use 100 Rheumatoid Arthritis
patients. Half the patients will enter the study when in acute flare
while the others will enter when they are not in an acute state. Both
groups will be followed prospectively. The product of the research
would be an improved outcome measure for public policy studies
relevant to arthritis.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
arthritisbehavioral /social science research tagclinical researchdata collection methodology /evaluationhealth care cost /financinghealth care policyhealth services research taghealth surveyshuman subjectmusculoskeletal disorderoutcomes researchpainpreferencequality of lifequestionnaires
National Institute of Arthritis and Musculoskeletal and Skin Diseases
CFDA Code
DUNS Number
804355790
UEI
UYTTZT6G9DT1
Project Start Date
01-March-1999
Project End Date
29-February-2000
Budget Start Date
01-October-1998
Budget End Date
30-September-1999
Project Funding Information for 1999
Total Funding
$114,229
Direct Costs
Indirect Costs
Year
Funding IC
FY Total Cost by IC
1999
National Institute of Arthritis and Musculoskeletal and Skin Diseases
$114,229
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5P60AR040770-08 0006
Publications
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No Publications available for 5P60AR040770-08 0006
Patents
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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Clinical Studies
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History
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