Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/114908
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dc.contributor.authorFerreira, Pedro Lopes-
dc.contributor.authorGenrinho, Inês-
dc.contributor.authorSantiago, Tânia-
dc.contributor.authorCarones, Adriana-
dc.contributor.authorMazeda, Carolina-
dc.contributor.authorBarcelos, Anabela-
dc.contributor.authorBeirão, Tiago-
dc.contributor.authorCosta, Flávio-
dc.contributor.authorSantos, Inês-
dc.contributor.authorCouto, Maura-
dc.contributor.authorRato, Maria-
dc.contributor.authorTerroso, Georgina-
dc.contributor.authorMonteiro, Paulo-
dc.date.accessioned2024-04-17T10:08:08Z-
dc.date.available2024-04-17T10:08:08Z-
dc.date.issued2023-01-14-
dc.identifier.issn1660-4601pt
dc.identifier.urihttps://hdl.handle.net/10316/114908-
dc.description.abstract(1) Background: The UCLA GIT 2.0 questionnaire has been recognized as a feasible and reliable instrument to assess gastrointestinal (GI) symptoms in systemic sclerosis (SSc) patients and their impact on quality of life. The aim of this study was to create and validate UCLA GIT 2.0 for Portuguese patients with SSc. (2) Methods: A multi-center study was conducted enrolling SSc patients. UCLA GIT 2.0 was validated in Portuguese using reliability (internal consistency, item -total correlation, and reproducibility) and validity (content, construct, and criterion) tests. Criterion tests included EQ-5D and SF-36v2. Social-demographic and clinical data were collected. (3) Results: 102 SSc patients were included, 82.4% of them female, and with a mean sample age of 57.0 ± 12.5 years old. The limited form of SSc was present in 62% of the patients and 56.9% had fewer than five years of disease duration. Almost 60% presented with SSc-GI involvement with a negative impact on quality of life. The means for SF-36v2 were 39.3 ± 10.3 in the physical component summary and 47.5 ± 12.1 in the mental component summary. Total GI score, reported as mild in 57.8% of the patients, was highly reliable (ICC = 0.912) and the Cronbach's alpha was 0.954. There was a high correlation between the total GI score and EQ-5D-5L and SF-36v2 scores. (4) Conclusion: The Portuguese version of UCLA GIT 2.0 showed good psychometric properties and can be used in research and clinical practice.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationCEISUC/CIBB is funded by national funds through FCT Foundation for Science and Technology, I.P., under the Multiannual Financing of R&D Units 2020–2023.pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectsystemic sclerosispt
dc.subjectgastrointestinal tractpt
dc.subjectUCLA GIT 2.0pt
dc.subjectquality of lifept
dc.subject.meshHumanspt
dc.subject.meshFemalept
dc.subject.meshAdultpt
dc.subject.meshMiddle Agedpt
dc.subject.meshAgedpt
dc.subject.meshQuality of Lifept
dc.subject.meshReproducibility of Resultspt
dc.subject.meshPortugalpt
dc.subject.meshSeverity of Illness Indexpt
dc.subject.meshPsychometricspt
dc.subject.meshSurveys and Questionnairespt
dc.subject.meshGastrointestinal Diseasespt
dc.subject.meshScleroderma, Systemicpt
dc.titleCreation and Validation of a Portuguese Version of the UCLA Scleroderma Clinical Trial Consortium Gastrointestinal Tract Instrumentpt
dc.typearticle-
degois.publication.firstPage1553pt
degois.publication.issue2pt
degois.publication.titleInternational Journal of Environmental Research and Public Healthpt
dc.peerreviewedyespt
dc.identifier.doi10.3390/ijerph20021553pt
degois.publication.volume20pt
dc.date.embargo2023-01-14*
uc.date.periodoEmbargo0pt
item.cerifentitytypePublications-
item.languageiso639-1en-
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
crisitem.author.researchunitCEISUC - Center for Health Studies and Research of the University of Coimbra-
crisitem.author.orcid0000-0002-9448-9542-
Appears in Collections:I&D CEISUC - Artigos em Revistas Internacionais
FEUC- Artigos em Revistas Internacionais
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This item is licensed under a Creative Commons License Creative Commons