Spanish adaptation and validation of the child‐ and parent‐report cystic fibrosis questionnaire‐revised (CFQ‐R)

dc.contributor.authorBlanco Orive, Paula
dc.contributor.authorDel Corral Núñez-Flores, Tamara
dc.contributor.authorMartín Casas, Patricia
dc.contributor.authorCebrià I Iranzo, Maria Àngels
dc.contributor.authorGodoy Nieto, Cristina
dc.contributor.authorLópez De Uralde Villanueva, Ibai Julio
dc.date.accessioned2024-04-19T17:26:48Z
dc.date.available2024-04-19T17:26:48Z
dc.date.issued2023-09-13
dc.description2023 Acuerdos transformativos CRUE
dc.description.abstractObjective To evaluate the psychometric properties of the Spanish versions of the child- and parent-report cystic fibrosis questionnaire-revised (CFQ-R). Methods A Spanish adaptation of the CFQ-R was performed; 68 children with CF (6−13 years) and their parents completed the child- and parent-report CFQ-R, respectively, and the Revidierter KINDer Lebensqualitätsfragebogen (KINDL) questionnaire. The CFQ-R was completed twice, 7−10 days apart, and its psychometric properties were analyzed. Results The internal consistency of both CFQ-R versions was adequate (child-report version, Cronbach's α >.60 for all domains except “Treatment Burden” [α = .42] and “Social Functioning” [α = .57]; parent-report version, α > .60 for all domains except “Social Functioning” [α = .58]). For the child-report version, the lowest measurement error was for “Emotional Functioning” (standard error of measurement [SEM]: 8.3%; minimal detectable change [MDC90]: 19.3%), and the highest was for “Body Image” (SEM: 15%; MDC90: 35%). For the parent-report version, the lowest measurement error was for “Physical Functioning” (SEM: 7.1%; MDC90: 16.5%), and the highest was for “Weight” (SEM: 17.2%; MDC90; 40.1%). The correlation between the versions showed higher agreement for the domains related to observable signs (“Physical Functioning”) and lower agreement for “Emotional Functioning.” There was a significant correlation between the CFQ-R and KINDL. Conclusion Both the child- and parent-report versions of the Spanish CFQ-R have adequate reliability and validity for clinical and research purposes. These versions can be administered before and after starting modulator therapy to assess its effect on daily functioning. The MDC90 can help identify, with a high probability, whether real changes have occurred in the quality-of-life subscales in children with CF.
dc.description.departmentDepto. de Radiología, Rehabilitación y Fisioterapia
dc.description.facultyFac. de Enfermería, Fisioterapia y Podología
dc.description.fundingtypeAPC financiada por la UCM
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.doi10.1002/ppul.26671
dc.identifier.issn8755-6863
dc.identifier.issn1099-0496
dc.identifier.officialurlhttps://doi.org/10.1002/ppul.26671
dc.identifier.urihttps://hdl.handle.net/20.500.14352/103279
dc.issue.number12
dc.journal.titlePediatric Pulmonology
dc.language.isoeng
dc.page.final3457
dc.page.initial3447
dc.publisherWiley
dc.rightsAttribution-NonCommercial 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subject.cdu616.24-056.7
dc.subject.keywordchild
dc.subject.keywordcystic fibrosis
dc.subject.keywordquality of life
dc.subject.keywordreliability
dc.subject.keywordvalidity
dc.subject.ucmCiencias Biomédicas
dc.subject.unesco3299 Otras Especialidades Médicas
dc.titleSpanish adaptation and validation of the child‐ and parent‐report cystic fibrosis questionnaire‐revised (CFQ‐R)
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number58
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscovery8a4040d5-5669-4b4a-8f3d-c9e29d3aa91e

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