Literature DB >> 28477695

Validity and reliability of the LEMOCOT in the adult ARSACS population: A measure of lower limb coordination.

Isabelle Lessard1, Caroline Lavoie2, Isabelle Côté2, Jean Mathieu1, Bernard Brais3, Cynthia Gagnon4.   

Abstract

OBJECTIVE: Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neuromuscular disease leading to several impairments, including decrease of lower limb coordination. The Lower Extremity Motor Coordination Test (LEMOCOT) is an outcome measure recently developed for stroke population. The aim of this study was to document: 1) intra- and interrater reliability; 2) the standard error of measurement and minimal detectable change; and 3) the construct validity of the measurements obtained with the LEMOCOT in the adult ARSACS population.
RESULTS: The LEMOCOT has shown a good intra- and interrater reliability with an intraclass correlation coefficient ranging from 0.92 to 0.97 for both dominant and non-dominant side. The construct validity (hypothesis testing) is satisfying where LEMOCOT's score negatively correlated with participants' age (r=-0.74) and the score of the Scale for the Assessment and Rating of Ataxia (r=-0.86) and positively correlated with the balance and mobility tests (r=0.82 with the Berg Balance Scale, r=0.61 with the Six-Minute Walk Test, r=0.57 with the 10-Meter Walk Test). The LEMOCOT was also able to distinguish between patients according to disease stages.
CONCLUSION: The LEMOCOT is a valid and reliable tool to assess lower limb coordination in the ARSACS population for whom the lack of coordination is a common symptom.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ARSACS; LEMOCOT; Outcome assessment (health care); Recessive ataxia; Reliability; Validity

Mesh:

Year:  2017        PMID: 28477695     DOI: 10.1016/j.jns.2017.03.046

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  5 in total

1.  Development and validation of a disease severity index for ataxia of Charlevoix-Saguenay.

Authors:  Cynthia Gagnon; Bernard Brais; Isabelle Lessard; Caroline Lavoie; Isabelle Côté; Jean Mathieu
Journal:  Neurology       Date:  2019-09-18       Impact factor: 9.910

2.  An exploratory natural history of ataxia of Charlevoix-Saguenay: A 2-year follow-up.

Authors:  Cynthia Gagnon; Isabelle Lessard; Caroline Lavoie; Isabelle Côté; Raphaël St-Gelais; Jean Mathieu; Bernard Brais
Journal:  Neurology       Date:  2018-08-29       Impact factor: 9.910

3.  From motor performance to participation: a quantitative descriptive study in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Authors:  Cynthia Gagnon; Bernard Brais; Isabelle Lessard; Caroline Lavoie; Isabelle Côté; Jean Mathieu
Journal:  Orphanet J Rare Dis       Date:  2018-09-19       Impact factor: 4.123

Review 4.  Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration.

Authors:  Jaya Bagaria; Eva Bagyinszky; Seong Soo A An
Journal:  Int J Mol Sci       Date:  2022-01-04       Impact factor: 5.923

5.  Reliability and validity of digital health metrics for assessing arm and hand impairments in an ataxic disorder.

Authors:  Cynthia Gagnon; Olivier Lambercy; Christoph M Kanzler; Isabelle Lessard; Roger Gassert; Bernard Brais
Journal:  Ann Clin Transl Neurol       Date:  2022-02-27       Impact factor: 4.511

  5 in total

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