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Translation and Psychometric Evaluation of a Korean Version of the Amyotrophic Lateral Sclerosis-Specific Quality of Life - Revised

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dc.contributor.authorOh, Juyeon-
dc.contributor.authorHong, Gwi-Ryung Son-
dc.contributor.authorKim, Seung Hyun-
dc.contributor.authorKim, Jung A.-
dc.date.accessioned2022-07-14T17:01:28Z-
dc.date.available2022-07-14T17:01:28Z-
dc.date.issued2017-02-
dc.identifier.issn2167-8421-
dc.identifier.issn2167-9223-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/152957-
dc.description.abstractObjective: The objective was to translate the Amyotrophic Lateral Sclerosis-Specific Quality of Life-Revised instrument (ALSSQOL-R) into Korean and to examine the psychometric properties of the Korean amyotrophic lateral sclerosis (ALS) population. Methods: The translation involved forward and backward translation. The psychometric properties of the Korean version of the ALSSQOL-R (K-ALSSQOL-R) were tested by patients in an ALS multidisciplinary clinic in Korea (n = 120). The internal consistency, test-retest reliability, content validity, criterion-related validity, and construct validity were evaluated. Results: With regard to the reliability estimate, the internal consistency (Cronbach's alpha = 0.92) and the test retest reliability (ICC = 0.89) were good. With regard to the validity estimate, the K-ALSSQOL-R demonstrated concurrent validity with the McGill Quality of Life Single-Item Scale (r = 0.62) and the first question of the World Health Organisation QOL Instrument-Brief (WHOQOL-BREF) (r = 0.64). The convergent validity and discriminant validity were acceptable. The confirmatory factor analysis supported a six-factor model. Conclusion: The K-ALSSOQL-R can be used as a reliable and valid measure of QOL among Korean ALS patients.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherInforma Healthcare-
dc.titleTranslation and Psychometric Evaluation of a Korean Version of the Amyotrophic Lateral Sclerosis-Specific Quality of Life - Revised-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1080/21678421.2016.1249885-
dc.identifier.scopusid2-s2.0-85001950423-
dc.identifier.wosid000394404400013-
dc.identifier.bibliographicCitationAmyotrophic Lateral Sclerosis and Frontotemporal Degeneration, v.18, no.1-2, pp 92 - 98-
dc.citation.titleAmyotrophic Lateral Sclerosis and Frontotemporal Degeneration-
dc.citation.volume18-
dc.citation.number1-2-
dc.citation.startPage92-
dc.citation.endPage98-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.subject.keywordPlusCAREGIVERS-
dc.subject.keywordPlusCRITERIA-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusSCALE-
dc.subject.keywordAuthorAmyotrophic Lateral Sclerosis-
dc.subject.keywordAuthorpsychometrics-
dc.subject.keywordAuthorquality of life-
dc.subject.keywordAuthorreliability and validity-
dc.subject.keywordAuthortranslation-
dc.identifier.urlhttps://www.tandfonline.com/doi/full/10.1080/21678421.2016.1249885-
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