Assessing the Measurement Properties of the Self-Administered Amyotrophic Lateral Sclerosis Functional Rating Scale–Revised (ALSFRS-R): A Rasch Analysis

Author:

Mehdipour Ava1ORCID,Teshler Lizabeth1,Dal Bello-Haas Vanina1,Richardson Julie1,Beauchamp Marla1,Turnbull John2,Chum Marvin2,Johnston Wendy3,O’Connell Colleen4,Luth Westerly3,Kuspinar Ayse1

Affiliation:

1. McMaster University School of Rehabilitation Science, Faculty of Health Sciences, , Hamilton, Ontario , Canada

2. McMaster University Department of Medicine, Faculty of Health Sciences, , Hamilton, Ontario , Canada

3. University of Alberta Department of Medicine, Faculty of Medicine and Dentistry, , Edmonton, Alberta , Canada

4. Dalhousie Medicine New Brunswick Stan Cassidy Centre for Rehabilitation, , Fredericton, New Brunswick , Canada

Abstract

Abstract Objective The self-administered version of the Amyotrophic Lateral Sclerosis Functional Rating Scale–Revised (ALSFRS-R) is used to monitor function and disease progression in individuals with amyotrophic lateral sclerosis (ALS). However, the performance of the self-administered ALSFRS-R has not been assessed using Rasch Measurement Theory. Therefore, the purpose of this study was to examine the psychometric properties of the self-administered ALSFRS-R using Rasch analysis. Methods Rasch analysis was performed on self-administered ALSFRS-R data from individuals with ALS across Canada. The following 6 aspects of Rasch analysis were examined using RUMM2030: fit via residuals and chi-square statistics, targeting via person-item threshold maps, dependency via item residual correlations, unidimensionality through principal components analysis of residuals, reliability via person separation index, and stability through differential item functioning analyses for sex, age, and language. Results Analysis was performed on 122 participants (mean age: 52.9 years; 62.8% men). The overall scale demonstrated good fit, reliability, and stability; however, multidimensionality was found. To address this issue, items were divided into 3 subscales (bulbar, motor, and respiratory function), and Rasch analysis was performed for each subscale. The subscales demonstrated good fit, reliability, stability, and unidimensionality. However, there were still issues with item dependency for all subscale and targeting for bulbar and respiratory subscales. Conclusions The self-administered ALSFRS-R is reliable, internally valid, and stable across sex, age, and language subgroups; however, it is recommended that the ALSFRS-R be scored by subscale. Future studies can look at revising and/or adding items to tackle misfit, redundancy, and ceiling effects. Impact Self-administered measures are simple to administer and inexpensive. The self-administered ALSFRS-R was found to be psychometrically sound and can be used as a tool to monitor disease progression and function in ALS.

Funder

ALS Society of Canada Project

Publisher

Oxford University Press (OUP)

Subject

Physical Therapy, Sports Therapy and Rehabilitation

Reference31 articles.

1. Amyotrophic lateral sclerosis;Brown;N Engl J Med,2017

2. Amyotrophic lateral sclerosis;Mitchell;Lancet,2007

3. Amyotrophic lateral sclerosis;Es;Lancet,2017

4. The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function;Cedarbaum;J Neurol Sci,1999

5. ALSFRS-R. Amyotrophic lateral sclerosis and other motor neuron disorders;Gordon,2004

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