Threshold definitions for significant change on the timed 25‐foot walk and nine‐hole peg test in primary progressive multiple sclerosis

Author:

Koch Marcus W.12ORCID,Repovic Pavle3,Mostert Jop4,Bowen James D.3,Comtois Jacynthe56,Strijbis Eva7ORCID,Uitdehaag Bernard7,Cutter Gary8

Affiliation:

1. Department of Clinical Neurosciences University of Calgary Calgary Alberta Canada

2. Department of Community Health Sciences University of Calgary Calgary Alberta Canada

3. Multiple Sclerosis Center Swedish Neuroscience Institute Seattle Washington USA

4. Department of Neurology Rijnstate Hospital Arnhem The Netherlands

5. Department of Medicine, Neurology service Hôpital Maisonneuve‐Rosemont Montreal Quebec Canada

6. Département de neurosciences, Faculté de médecine Université de Montréal Montreal Quebec Canada

7. Department of Neurology, MS Center Amsterdam Amsterdam University Medical Centers Amsterdam The Netherlands

8. Department of Biostatistics University of Alabama at Birmingham Birmingham Alabama USA

Abstract

AbstractBackground and purposeThe timed 25‐foot walk (T25FW) and nine‐hole peg test (NHPT) exhibit random variability in the short term. A threshold of ≥20% change from baseline has been used to indicate true disability change, but other threshold definitions may be better suited to exclude false and include true change events. The aim of this study was to use patient‐level original trial data to investigate the short‐term variation in T25FW and NHPT, and to compare its extent with disability change at 12‐month follow‐up in people with primary progressive multiple sclerosis (PPMS).MethodsWe used original patient‐level data from PROMISE, a large PPMS trial. In this trial, three separate T25FW and NHPT measurements were performed 1 week apart during screening. We used these repeated measures to describe the extent of short‐term variation. We used binary logistic regression models to investigate the association between screening characteristics and unacceptable short‐term variation.ResultsThe traditional 20% threshold excluded a reasonable number of false change events, while also yielding a large number of change events at follow‐up. Increasing index values on the T25FW and NHPT were associated with higher short‐term variation.ConclusionsThe traditional ≥20% change threshold for the T25FW and NHPT represents a reasonable compromise between reducing the number of false change events and achieving the largest number of change events in people with PPMS. Our analyses inform the design of clinical trials in PPMS.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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