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January 14, 2003

Measuring the impact of MS on walking ability
The 12-Item MS Walking Scale (MSWS-12)

January 14, 2003 issue
60 (1) 31-36

Abstract

Objective: To develop a patient-based measure of walking ability in MS.
Methods: Twelve items describing the impact of MS on walking (12-Item MS Walking Scale [MSWS-12]) were generated from 30 patient interviews, expert opinion, and literature review. Preliminary psychometric evaluation (data quality, scaling assumptions, acceptability, reliability, validity) was undertaken in the data generated by 602 people from the MS Society membership database. Further psychometric evaluation (including comprehensive validity assessment, responsiveness, and relative efficiency) was conducted in two hospital-based samples: people with primary progressive MS (PPMS; n = 78) and people with relapses admitted for IV steroid treatment (n = 54).
Results: In all samples, missing data were low (≤3.8%), item test–retest reproducibility was high (≥0.78), scaling assumptions were satisfied, and reliability was high (≥0.94). Correlations between the MSWS-12 and other scales were consistent with a priori hypotheses. The MSWS-12 (relative efficiency = 1.0) was more responsive than the Functional Assessment of Multiple Sclerosis mobility scale (0.72), the 36-Item Short Form Health Survey physical functioning scale (0.33), the Expanded Disability Status Scale (0.03), the 25-ft Timed Walk Test (0.44), and Guy’s Neurologic Disability Scale lower limb disability item (0.10).
Conclusions: The MSWS-12 satisfies standard criteria as a reliable and valid patient-based measure of the impact of MS on walking. In these samples, the MSWS-12 was more responsive than other walking-based scales.

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Information & Authors

Information

Published In

Neurology®
Volume 60Number 1January 14, 2003
Pages: 31-36
PubMed: 12525714

Publication History

Received: January 24, 2002
Accepted: September 12, 2002
Published online: January 14, 2003
Published in print: January 14, 2003

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Authors

Affiliations & Disclosures

J. C. Hobart, PhD
From the Institute of Neurology (Drs. Hobart, Riazi, and Thompson), University College London; Health Services Research Unit (Dr. Lamping), London School of Hygiene and Tropical Medicine; and Department of Public Health and Primary Care (Dr. Fitzpatrick), University of Oxford, UK.
A. Riazi, PhD
From the Institute of Neurology (Drs. Hobart, Riazi, and Thompson), University College London; Health Services Research Unit (Dr. Lamping), London School of Hygiene and Tropical Medicine; and Department of Public Health and Primary Care (Dr. Fitzpatrick), University of Oxford, UK.
D. L. Lamping, PhD
From the Institute of Neurology (Drs. Hobart, Riazi, and Thompson), University College London; Health Services Research Unit (Dr. Lamping), London School of Hygiene and Tropical Medicine; and Department of Public Health and Primary Care (Dr. Fitzpatrick), University of Oxford, UK.
R. Fitzpatrick, PhD
From the Institute of Neurology (Drs. Hobart, Riazi, and Thompson), University College London; Health Services Research Unit (Dr. Lamping), London School of Hygiene and Tropical Medicine; and Department of Public Health and Primary Care (Dr. Fitzpatrick), University of Oxford, UK.
A. J. Thompson, MD
From the Institute of Neurology (Drs. Hobart, Riazi, and Thompson), University College London; Health Services Research Unit (Dr. Lamping), London School of Hygiene and Tropical Medicine; and Department of Public Health and Primary Care (Dr. Fitzpatrick), University of Oxford, UK.

Notes

Address correspondence and reprint requests to Dr. Jeremy C. Hobart, Derriford Hospital, Plymouth, Devon PL6 8DH, UK; e-mail: [email protected]

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