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Erschienen in: Journal of Neurology 7/2019

06.04.2019 | Original Communication

15-White Dots APP-Coo-Test: a reliable touch-screen application for assessing upper limb movement impairment in patients with cerebellar ataxias

verfasst von: Giuseppe Arcuria, Christian Marcotulli, Claudio Galasso, Francesco Pierelli, Carlo Casali

Erschienen in: Journal of Neurology | Ausgabe 7/2019

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Abstract

Background

The use of objective measurements is essential to assess disease progression and to evaluate the effectiveness of rehabilitation protocols and clinical treatments.

Aim

The purpose of this study was to develop a touch-screen application, that we named 15-White Dots APP-Coo-Test (15-WDACT), able to carry out quantitative and objective measurements of the rapid and coordinated upper limb movements, typically impaired in patients with cerebellar ataxias (CA).

Methods

A total of 87 CA patients and 170 healthy subjects participated in this study. The subject was asked to touch with their index finger a white dot, appearing consecutively and randomly on the screen at different positions, for a total of 15 dots per session. The score is the execution time of a single session.

Results

15-WDACT measurements have highly correlated with the scores obtained with the Scale for the Assessment and Rating of Ataxia (SARA), with the Composite Cerebellar Functional Severity (CCFS) and with the measurements obtained using two validated evaluating systems, i.e., the Nine Hole Pegboard test (9HPT) and the Click Test. We also observed high internal consistency and an excellent intra-rater and test–retest reliability. We found a small Standard Error of Measurement (SEM) and an excellent Minimal Detectable Change (MDC), indicating that even small variations in the 15-WDACT measurements are to be associated with real changes in performance.

Conclusions

We have concluded that 15-WDACT is an easy, fast and reliable tool to assess the severity of the upper limb ataxia in patients with CA.
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Literatur
1.
Zurück zum Zitat Bodranghien F, Bastian A, Casali C, Hallett M, Louis ED, Manto M et al (2016) Consensus paper: revisiting the symptoms and signs of cerebellar syndrome. Cerebellum 15(3):369–391CrossRefPubMedPubMedCentral Bodranghien F, Bastian A, Casali C, Hallett M, Louis ED, Manto M et al (2016) Consensus paper: revisiting the symptoms and signs of cerebellar syndrome. Cerebellum 15(3):369–391CrossRefPubMedPubMedCentral
2.
Zurück zum Zitat Patel M, Isaacs CJ, Seyer L, Brigatti K, Gelbard S, Strawer C et al (2016) Progression of Friedreich ataxia: quantitative characterization over 5 years. Ann Clin Transl Neurol 3:684–694CrossRefPubMedPubMedCentral Patel M, Isaacs CJ, Seyer L, Brigatti K, Gelbard S, Strawer C et al (2016) Progression of Friedreich ataxia: quantitative characterization over 5 years. Ann Clin Transl Neurol 3:684–694CrossRefPubMedPubMedCentral
3.
Zurück zum Zitat Reetz K, Dogan I, Hilgers RD, Giunti P, Mariotti C, Durr A et al (2016) Biological and clinical characteristics of the European Friedreich’s Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data. Lancet Neurol 15:1346–1354CrossRefPubMed Reetz K, Dogan I, Hilgers RD, Giunti P, Mariotti C, Durr A et al (2016) Biological and clinical characteristics of the European Friedreich’s Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data. Lancet Neurol 15:1346–1354CrossRefPubMed
4.
Zurück zum Zitat Diallo A, Jacobi H, Cook A, Labrum R, Durr A, Brice A et al (2018) Survival in patients with spinocerebellar ataxias types 1,2,3 and 6 (EUROSCA): a longitudinal cohort study. Lancet Neurol 17:327–334CrossRefPubMed Diallo A, Jacobi H, Cook A, Labrum R, Durr A, Brice A et al (2018) Survival in patients with spinocerebellar ataxias types 1,2,3 and 6 (EUROSCA): a longitudinal cohort study. Lancet Neurol 17:327–334CrossRefPubMed
5.
Zurück zum Zitat Yabe I, Matsushima M (2008) Usefulness of the scale for the assessment and rating of ataxia (SARA). J Neurol Sci 266:164–166CrossRefPubMed Yabe I, Matsushima M (2008) Usefulness of the scale for the assessment and rating of ataxia (SARA). J Neurol Sci 266:164–166CrossRefPubMed
6.
Zurück zum Zitat Schmitz-Hubsch T et al (2006) Scale for the assessment of ataxia: development of a new clinical scale. Neurology 66:1717–1720CrossRef Schmitz-Hubsch T et al (2006) Scale for the assessment of ataxia: development of a new clinical scale. Neurology 66:1717–1720CrossRef
7.
Zurück zum Zitat Weyer A, Abele M, Schmitz-Hubsch T (2007) Reliability and validity of the scale for the assessment and rating of ataxia: a study in 64 ataxia patients. Mov Disord 22:1633–1637CrossRefPubMed Weyer A, Abele M, Schmitz-Hubsch T (2007) Reliability and validity of the scale for the assessment and rating of ataxia: a study in 64 ataxia patients. Mov Disord 22:1633–1637CrossRefPubMed
8.
Zurück zum Zitat Bürk K, Sival DA (2018) Scales for clinical evaluation of cerebellar disorders. Hand Clin Neurol 154:329–339CrossRef Bürk K, Sival DA (2018) Scales for clinical evaluation of cerebellar disorders. Hand Clin Neurol 154:329–339CrossRef
9.
Zurück zum Zitat Tanguy Melac A, Mariotti C, Filipovic Pierucci A, Giunti P, Arpa J, Boesch S et al (2018) Friedreich and dominant ataxias: quantitative differences in cerebellar dysfunction measurements. J Neurol Neurosurg Psychiatry 89:559–565CrossRefPubMed Tanguy Melac A, Mariotti C, Filipovic Pierucci A, Giunti P, Arpa J, Boesch S et al (2018) Friedreich and dominant ataxias: quantitative differences in cerebellar dysfunction measurements. J Neurol Neurosurg Psychiatry 89:559–565CrossRefPubMed
10.
Zurück zum Zitat Schmitz-Hübsch T, Tezenas-Du-Montcel S, Baliko L, Boesch S, Bonato S, Fancellu R et al (2005) Reliability and validity of the international cooperative ataxia rating scale: a study in 156 spinocerebellar ataxia patients. Mov Disord 21:699–704CrossRef Schmitz-Hübsch T, Tezenas-Du-Montcel S, Baliko L, Boesch S, Bonato S, Fancellu R et al (2005) Reliability and validity of the international cooperative ataxia rating scale: a study in 156 spinocerebellar ataxia patients. Mov Disord 21:699–704CrossRef
11.
Zurück zum Zitat Tison F, Yekhlef F (2002) Application of the international cooperative ataxia scale rating in multiple system atrophy. Mov Disord 17(6):1248–1254CrossRefPubMed Tison F, Yekhlef F (2002) Application of the international cooperative ataxia scale rating in multiple system atrophy. Mov Disord 17(6):1248–1254CrossRefPubMed
12.
Zurück zum Zitat Schmitz-Hübsch T, Giunti P, Stephenson DA, Globas C, Baliko L, Saccà F et al (2008) SCA Functional Index—usefulness of a compound performance measure in spinocerebellar ataxia patients. Neurology 71:486–492CrossRefPubMed Schmitz-Hübsch T, Giunti P, Stephenson DA, Globas C, Baliko L, Saccà F et al (2008) SCA Functional Index—usefulness of a compound performance measure in spinocerebellar ataxia patients. Neurology 71:486–492CrossRefPubMed
13.
Zurück zum Zitat Schmitz-Hübsch T, Fimmers R, Rakowicz M, Rola R, Zdzienicka E, Fancellu R et al (2010) Responsiveness of different rating instruments in spinocerebellar ataxia patients. Neurology 74:678–684CrossRefPubMed Schmitz-Hübsch T, Fimmers R, Rakowicz M, Rola R, Zdzienicka E, Fancellu R et al (2010) Responsiveness of different rating instruments in spinocerebellar ataxia patients. Neurology 74:678–684CrossRefPubMed
14.
Zurück zum Zitat du Montcel ST, Charles P, Ribai P, Goizet C, Le Bayon A, Labauge P et al (2008) Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment. Brain 131:1352–1361CrossRefPubMed du Montcel ST, Charles P, Ribai P, Goizet C, Le Bayon A, Labauge P et al (2008) Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment. Brain 131:1352–1361CrossRefPubMed
15.
Zurück zum Zitat Mathiowetz V, Weber K, Kashman N, Volland G (1985) Adult norms for the nine hole peg test of finger dexterity. Occup Ther J Res 5(1):24–38CrossRef Mathiowetz V, Weber K, Kashman N, Volland G (1985) Adult norms for the nine hole peg test of finger dexterity. Occup Ther J Res 5(1):24–38CrossRef
16.
Zurück zum Zitat Oxford Grice K, Vogel KA, Le V, Mitchell A, Muniz S, Vollmer MA (2003) Adult norms for a commercially available nine hole peg test for finger dexterity. Am J Occup Ther 57(5):570–573CrossRefPubMed Oxford Grice K, Vogel KA, Le V, Mitchell A, Muniz S, Vollmer MA (2003) Adult norms for a commercially available nine hole peg test for finger dexterity. Am J Occup Ther 57(5):570–573CrossRefPubMed
17.
Zurück zum Zitat Paap BK, Roeske S, Durr A, Schöls L, Ashizawa T, Boesch S, Bunn LM et al (2016) Standardized assessment of hereditary ataxia patients in clinical studies. Mov Disord Clin Pract 3(3):230–240CrossRefPubMedPubMedCentral Paap BK, Roeske S, Durr A, Schöls L, Ashizawa T, Boesch S, Bunn LM et al (2016) Standardized assessment of hereditary ataxia patients in clinical studies. Mov Disord Clin Pract 3(3):230–240CrossRefPubMedPubMedCentral
18.
Zurück zum Zitat Tanguy Melac A, Mariotti C, Filipovic Pierucci A, Giunti P, Arpa J, Boesch S, Klopstock T, Müller Vom Hagen J, Klockgether T, Bürk K, Schulz JB, Reetz K, Pandolfo M, Durr A, Tezenas du Montcel S (2018) Friedreich and dominant ataxias: quantitative differences in cerebellar dysfunction measurements. J Neurol Neurosurg Psychiatry 89(6):559–565CrossRefPubMed Tanguy Melac A, Mariotti C, Filipovic Pierucci A, Giunti P, Arpa J, Boesch S, Klopstock T, Müller Vom Hagen J, Klockgether T, Bürk K, Schulz JB, Reetz K, Pandolfo M, Durr A, Tezenas du Montcel S (2018) Friedreich and dominant ataxias: quantitative differences in cerebellar dysfunction measurements. J Neurol Neurosurg Psychiatry 89(6):559–565CrossRefPubMed
19.
Zurück zum Zitat Portney LG, Watkins MP (2009) Foundations of clinical research: applications to practice. Pearson/Prentice Hall, Upper Saddle River Portney LG, Watkins MP (2009) Foundations of clinical research: applications to practice. Pearson/Prentice Hall, Upper Saddle River
20.
Zurück zum Zitat Baumgartner TA, Chung H (2001) Confidence limits for intraclass reliability coefficients. Meas Phys Educ Exerc Sci 5:179–188CrossRef Baumgartner TA, Chung H (2001) Confidence limits for intraclass reliability coefficients. Meas Phys Educ Exerc Sci 5:179–188CrossRef
21.
22.
Zurück zum Zitat Donoghue D, Stokes EK (2009) How much change is true change? The minimum detectable change of the Berg Balance Scale in elderly people. J Rehabil Med 41:343–346CrossRefPubMed Donoghue D, Stokes EK (2009) How much change is true change? The minimum detectable change of the Berg Balance Scale in elderly people. J Rehabil Med 41:343–346CrossRefPubMed
23.
Zurück zum Zitat Haley SM, Fragala-Pinkham MA (2006) Interpreting change scores of tests and measures used in physical therapy. Phys Ther 86:735–743PubMed Haley SM, Fragala-Pinkham MA (2006) Interpreting change scores of tests and measures used in physical therapy. Phys Ther 86:735–743PubMed
24.
Zurück zum Zitat Serrao M, Pierelli F, Ranavolo A, Draicchio F, Conte C, Casali C et al (2012) Gait pattern in inherited cerebellar ataxias. Cerebellum 11(1):194–211CrossRefPubMed Serrao M, Pierelli F, Ranavolo A, Draicchio F, Conte C, Casali C et al (2012) Gait pattern in inherited cerebellar ataxias. Cerebellum 11(1):194–211CrossRefPubMed
25.
Zurück zum Zitat Fujioka S, Sundal C, Zbigniew K (2013) Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics. Orphanet J Rare Dis 18(8):14CrossRef Fujioka S, Sundal C, Zbigniew K (2013) Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics. Orphanet J Rare Dis 18(8):14CrossRef
26.
Zurück zum Zitat Schols L, Bauer P, Schmidt T, Schulte T, Riess O (2004) Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol 3:291–304CrossRef Schols L, Bauer P, Schmidt T, Schulte T, Riess O (2004) Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol 3:291–304CrossRef
27.
Zurück zum Zitat Basri R, Yabe I, Soma H, Sasaki H (2007) Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families. J Hum Genet 52:848–855CrossRefPubMed Basri R, Yabe I, Soma H, Sasaki H (2007) Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families. J Hum Genet 52:848–855CrossRefPubMed
Metadaten
Titel
15-White Dots APP-Coo-Test: a reliable touch-screen application for assessing upper limb movement impairment in patients with cerebellar ataxias
verfasst von
Giuseppe Arcuria
Christian Marcotulli
Claudio Galasso
Francesco Pierelli
Carlo Casali
Publikationsdatum
06.04.2019
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Neurology / Ausgabe 7/2019
Print ISSN: 0340-5354
Elektronische ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-019-09299-9

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