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Development and exploration of a Japanese version of the cerebral palsy quality of life for children questionnaire for primary caregivers: a pilot study

[Purpose] We aimed to translate and validate a Japanese language version of the cerebral palsy quality of life for children questionnaire for primary caregivers and assess the relationship between quality of life of Japanese parents and their children’s motor skills. [Participants and Methods] Fifty...

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Autores principales: Mutoh, Tomoko, Mutoh, Tatsushi, Kurosaki, Hiromi, Shimomura, Hideo, Taki, Yasuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Society of Physical Therapy Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751053/
https://www.ncbi.nlm.nih.gov/pubmed/31631945
http://dx.doi.org/10.1589/jpts.31.724
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author Mutoh, Tomoko
Mutoh, Tatsushi
Kurosaki, Hiromi
Shimomura, Hideo
Taki, Yasuyuki
author_facet Mutoh, Tomoko
Mutoh, Tatsushi
Kurosaki, Hiromi
Shimomura, Hideo
Taki, Yasuyuki
author_sort Mutoh, Tomoko
collection PubMed
description [Purpose] We aimed to translate and validate a Japanese language version of the cerebral palsy quality of life for children questionnaire for primary caregivers and assess the relationship between quality of life of Japanese parents and their children’s motor skills. [Participants and Methods] Fifty children (aged 4 to 12 years) and their parents (mothers) were enrolled. The parent-proxy version of the cerebral palsy quality of life for children questionnaire translated to Japanese was administered, and a validation study was performed using Cronbach’s α as the key metric. The relationships between the parents’ quality of life and children’s Gross Motor Function Classification Scale levels were analyzed. [Results] We found that the age of the children and their parents and gender of the children were not significant factors affecting the quality of life domains. Significantly high values of internal consistency were detected among items within each quality of life domain, wherein Cronbach’s α was between 0.72 and 0.89. Two quality of life domains (Emotional well-being and Feeling about functioning) were significantly associated with Gross Motor Function Classification Scale levels. [Conclusion] Our data suggest that the original English version of the cerebral palsy quality of life for children questionnaire for primary caregivers was successfully translated to Japanese for use by Japanese-speaking parents caring for their children.
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spelling pubmed-67510532019-10-18 Development and exploration of a Japanese version of the cerebral palsy quality of life for children questionnaire for primary caregivers: a pilot study Mutoh, Tomoko Mutoh, Tatsushi Kurosaki, Hiromi Shimomura, Hideo Taki, Yasuyuki J Phys Ther Sci Original Article [Purpose] We aimed to translate and validate a Japanese language version of the cerebral palsy quality of life for children questionnaire for primary caregivers and assess the relationship between quality of life of Japanese parents and their children’s motor skills. [Participants and Methods] Fifty children (aged 4 to 12 years) and their parents (mothers) were enrolled. The parent-proxy version of the cerebral palsy quality of life for children questionnaire translated to Japanese was administered, and a validation study was performed using Cronbach’s α as the key metric. The relationships between the parents’ quality of life and children’s Gross Motor Function Classification Scale levels were analyzed. [Results] We found that the age of the children and their parents and gender of the children were not significant factors affecting the quality of life domains. Significantly high values of internal consistency were detected among items within each quality of life domain, wherein Cronbach’s α was between 0.72 and 0.89. Two quality of life domains (Emotional well-being and Feeling about functioning) were significantly associated with Gross Motor Function Classification Scale levels. [Conclusion] Our data suggest that the original English version of the cerebral palsy quality of life for children questionnaire for primary caregivers was successfully translated to Japanese for use by Japanese-speaking parents caring for their children. The Society of Physical Therapy Science 2019-09-05 2019-09 /pmc/articles/PMC6751053/ /pubmed/31631945 http://dx.doi.org/10.1589/jpts.31.724 Text en 2019©by the Society of Physical Therapy Science. Published by IPEC Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Article
Mutoh, Tomoko
Mutoh, Tatsushi
Kurosaki, Hiromi
Shimomura, Hideo
Taki, Yasuyuki
Development and exploration of a Japanese version of the cerebral palsy quality of life for children questionnaire for primary caregivers: a pilot study
title Development and exploration of a Japanese version of the cerebral palsy quality of life for children questionnaire for primary caregivers: a pilot study
title_full Development and exploration of a Japanese version of the cerebral palsy quality of life for children questionnaire for primary caregivers: a pilot study
title_fullStr Development and exploration of a Japanese version of the cerebral palsy quality of life for children questionnaire for primary caregivers: a pilot study
title_full_unstemmed Development and exploration of a Japanese version of the cerebral palsy quality of life for children questionnaire for primary caregivers: a pilot study
title_short Development and exploration of a Japanese version of the cerebral palsy quality of life for children questionnaire for primary caregivers: a pilot study
title_sort development and exploration of a japanese version of the cerebral palsy quality of life for children questionnaire for primary caregivers: a pilot study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751053/
https://www.ncbi.nlm.nih.gov/pubmed/31631945
http://dx.doi.org/10.1589/jpts.31.724
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