Measuring Health Related Quality of Life in Veterans With Stroke
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|ClinicalTrials.gov Identifier: NCT00123357|
Recruitment Status : Completed
First Posted : July 22, 2005
Last Update Posted : April 7, 2015
|Condition or disease|
|Stroke Quality of Life Rehabilitation|
Approximately 11,000 veterans annually are hospitalized with a newly acquired incident stroke. Based on American Heart Association ratios of stroke incidence and prevalence, up to 80,000 veterans may be stroke survivors. The assessment of outcomes in stroke survivors is important for clinical practice and research, yet there is no consensus on the best measures of stroke outcome in either clinical practice or research. We have developed a new stroke-specific outcome measure, the Stroke Impact Scale (SIS), to capture physical function and other dimensions of health-related quality of life.
The major research questions in this investigation are: 1) Does the SIS have concurrent and discriminate validity in a veteran stroke population when compared to the FIM, Rankin, and the SF-36V? 2) What effect does mode of administration have on response rates, bias, data quality, reliability and validity, SIS domain scores, and cost of data collection? 3) What factors differentiate responders and non-responders? 4) Will the SIS scores predict health care costs and utilization?
Using ICD-9 discharge codes and electronic medical records, patients were screened for a valid diagnosis of stroke. At three months post-stroke, patients were randomly assigned to receive a mailed SIS instrument or SIS via telephone interview. At four months post-stroke, all respondents were evaluated using the Functional Independence Measure and SF-36V by telephone.
|Study Type :||Observational|
|Estimated Enrollment :||800 participants|
|Official Title:||Measuring Health Related Quality of Life in Veterans With Stroke|
|Actual Study Completion Date :||March 2003|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00123357
|United States, Illinois|
|Kansas City VA Medical Center, Kansas City, MO|
|Kansas City, Illinois, United States, 64128|
|Principal Investigator:||Dean M. Reker, PhD RN BS||Kansas City VA Medical Center, Kansas City, MO|
|Principal Investigator:||Pamela W. Duncan, PhD MA BS||North Florida/South Georgia Veterans Health System, Gainesville, FL|