Computer task performance by subjects with Duchenne muscular dystrophy
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.2147/NDT.S87735 http://repositorio.unifesp.br/handle/11600/46085 |
Resumo: | Aims: Two specific objectives were established to quantify computer task performance among people with Duchenne muscular dystrophy (DMD). First, we compared simple computational task performance between subjects with DMD and age-matched typically developing (TD) subjects. Second, we examined correlations between the ability of subjects with DMD to learn the computational task and their motor functionality, age, and initial task performance. Method: The study included 84 individuals (42 with DMD, mean age of 18 +/- 5.5 years, and 42 age-matched controls). They executed a computer maze task all participants performed the acquisition (20 attempts) and retention (five attempts) phases, repeating the same maze. A different maze was used to verify transfer performance (five attempts). The Motor Function Measure Scale was applied, and the results were compared with maze task performance. Results: In the acquisition phase, a significant decrease was found in movement time (MT) between the first and last acquisition block, but only for the DMD group. For the DMD group, MT during transfer was shorter than during the first acquisition block, indicating improvement from the first acquisition block to transfer. In addition, the TD group showed shorter MT than the DMD group across the study. Conclusion: DMD participants improved their performance after practicing a computational task however, the difference in MT was present in all attempts among DMD and control subjects. Computational task improvement was positively influenced by the initial performance of individuals with DMD. In turn, the initial performance was influenced by their distal functionality but not their age or overall functionality. |
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spelling |
Computer task performance by subjects with Duchenne muscular dystrophycomputer taskmotor learningDuchenne muscular dystrophymovement timeMotor Function MeasureFunction Measure ScaleVirtual-RealityNeuromuscular DiseasesChildrenEnvironmentsIndividualsDisabilityWeaknessProfileAims: Two specific objectives were established to quantify computer task performance among people with Duchenne muscular dystrophy (DMD). First, we compared simple computational task performance between subjects with DMD and age-matched typically developing (TD) subjects. Second, we examined correlations between the ability of subjects with DMD to learn the computational task and their motor functionality, age, and initial task performance. Method: The study included 84 individuals (42 with DMD, mean age of 18 +/- 5.5 years, and 42 age-matched controls). They executed a computer maze task all participants performed the acquisition (20 attempts) and retention (five attempts) phases, repeating the same maze. A different maze was used to verify transfer performance (five attempts). The Motor Function Measure Scale was applied, and the results were compared with maze task performance. Results: In the acquisition phase, a significant decrease was found in movement time (MT) between the first and last acquisition block, but only for the DMD group. For the DMD group, MT during transfer was shorter than during the first acquisition block, indicating improvement from the first acquisition block to transfer. In addition, the TD group showed shorter MT than the DMD group across the study. Conclusion: DMD participants improved their performance after practicing a computational task however, the difference in MT was present in all attempts among DMD and control subjects. Computational task improvement was positively influenced by the initial performance of individuals with DMD. In turn, the initial performance was influenced by their distal functionality but not their age or overall functionality.School of Medicine of ABC, Santo Andre, BrazilDepartment of Medicine, Paulista School of Medicine, Federal University of São Paulo, São Paulo, BrazilCenter for Neurosciences, University of São Paulo, São Paulo, BrazilPost-graduate Program in Rehabilitation Sciences, Faculty of Medicine, University of São Paulo, São Paulo, BrazilSchool of Arts, Sciences and Humanities, University of São Paulo, São Paulo, BrazilDepartment of Medicine, Paulista School of Medicine, Federal University of São Paulo, São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)FAPESP: 2012/16970-6Dove Medical Press Ltd2018-07-26T17:30:29Z2018-07-26T17:30:29Z2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion41-48http://dx.doi.org/10.2147/NDT.S87735Neuropsychiatric Disease And Treatment. Albany, v. 12, p. 41-48, 2016.10.2147/NDT.S877351178-2021http://repositorio.unifesp.br/handle/11600/46085WOS:000367284300002engNeuropsychiatric Disease And Treatmentinfo:eu-repo/semantics/openAccessPinheiro Malheiros, Silvia Reginada Silva, Talita Dias [UNIFESP]Favero, Francis Meire [UNIFESP]de Abreu, Luiz CarlosFregni, FelipeRibeiro, Denise Cardosode Mello Monteiro, Carlos Bandeirareponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2021-10-04T21:26:14Zoai:repositorio.unifesp.br/:11600/46085Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652021-10-04T21:26:14Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Computer task performance by subjects with Duchenne muscular dystrophy |
title |
Computer task performance by subjects with Duchenne muscular dystrophy |
spellingShingle |
Computer task performance by subjects with Duchenne muscular dystrophy Pinheiro Malheiros, Silvia Regina computer task motor learning Duchenne muscular dystrophy movement timeMotor Function Measure Function Measure Scale Virtual-Reality Neuromuscular Diseases Children Environments Individuals Disability Weakness Profile |
title_short |
Computer task performance by subjects with Duchenne muscular dystrophy |
title_full |
Computer task performance by subjects with Duchenne muscular dystrophy |
title_fullStr |
Computer task performance by subjects with Duchenne muscular dystrophy |
title_full_unstemmed |
Computer task performance by subjects with Duchenne muscular dystrophy |
title_sort |
Computer task performance by subjects with Duchenne muscular dystrophy |
author |
Pinheiro Malheiros, Silvia Regina |
author_facet |
Pinheiro Malheiros, Silvia Regina da Silva, Talita Dias [UNIFESP] Favero, Francis Meire [UNIFESP] de Abreu, Luiz Carlos Fregni, Felipe Ribeiro, Denise Cardoso de Mello Monteiro, Carlos Bandeira |
author_role |
author |
author2 |
da Silva, Talita Dias [UNIFESP] Favero, Francis Meire [UNIFESP] de Abreu, Luiz Carlos Fregni, Felipe Ribeiro, Denise Cardoso de Mello Monteiro, Carlos Bandeira |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Pinheiro Malheiros, Silvia Regina da Silva, Talita Dias [UNIFESP] Favero, Francis Meire [UNIFESP] de Abreu, Luiz Carlos Fregni, Felipe Ribeiro, Denise Cardoso de Mello Monteiro, Carlos Bandeira |
dc.subject.por.fl_str_mv |
computer task motor learning Duchenne muscular dystrophy movement timeMotor Function Measure Function Measure Scale Virtual-Reality Neuromuscular Diseases Children Environments Individuals Disability Weakness Profile |
topic |
computer task motor learning Duchenne muscular dystrophy movement timeMotor Function Measure Function Measure Scale Virtual-Reality Neuromuscular Diseases Children Environments Individuals Disability Weakness Profile |
description |
Aims: Two specific objectives were established to quantify computer task performance among people with Duchenne muscular dystrophy (DMD). First, we compared simple computational task performance between subjects with DMD and age-matched typically developing (TD) subjects. Second, we examined correlations between the ability of subjects with DMD to learn the computational task and their motor functionality, age, and initial task performance. Method: The study included 84 individuals (42 with DMD, mean age of 18 +/- 5.5 years, and 42 age-matched controls). They executed a computer maze task all participants performed the acquisition (20 attempts) and retention (five attempts) phases, repeating the same maze. A different maze was used to verify transfer performance (five attempts). The Motor Function Measure Scale was applied, and the results were compared with maze task performance. Results: In the acquisition phase, a significant decrease was found in movement time (MT) between the first and last acquisition block, but only for the DMD group. For the DMD group, MT during transfer was shorter than during the first acquisition block, indicating improvement from the first acquisition block to transfer. In addition, the TD group showed shorter MT than the DMD group across the study. Conclusion: DMD participants improved their performance after practicing a computational task however, the difference in MT was present in all attempts among DMD and control subjects. Computational task improvement was positively influenced by the initial performance of individuals with DMD. In turn, the initial performance was influenced by their distal functionality but not their age or overall functionality. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 2018-07-26T17:30:29Z 2018-07-26T17:30:29Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.2147/NDT.S87735 Neuropsychiatric Disease And Treatment. Albany, v. 12, p. 41-48, 2016. 10.2147/NDT.S87735 1178-2021 http://repositorio.unifesp.br/handle/11600/46085 WOS:000367284300002 |
url |
http://dx.doi.org/10.2147/NDT.S87735 http://repositorio.unifesp.br/handle/11600/46085 |
identifier_str_mv |
Neuropsychiatric Disease And Treatment. Albany, v. 12, p. 41-48, 2016. 10.2147/NDT.S87735 1178-2021 WOS:000367284300002 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Neuropsychiatric Disease And Treatment |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
41-48 |
dc.publisher.none.fl_str_mv |
Dove Medical Press Ltd |
publisher.none.fl_str_mv |
Dove Medical Press Ltd |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268323587686400 |