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

ObjectiveTo evaluate the psychometric properties of the Spanish versions of the child‐ and parent‐report cystic fibrosis questionnaire‐revised (CFQ‐R).MethodsA 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...

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Published in:Pediatric pulmonology 2023-12, Vol.58 (12), p.3447-3457
Main Authors: Blanco‐Orive, Paula, del Corral, Tamara, Martín‐Casas, Patricia, Cebrià I Iranzo, Maria Àngels, Godoy‐Nieto, Cristina, López‐de‐Uralde‐Villanueva, Ibai
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container_end_page 3457
container_issue 12
container_start_page 3447
container_title Pediatric pulmonology
container_volume 58
creator Blanco‐Orive, Paula
del Corral, Tamara
Martín‐Casas, Patricia
Cebrià I Iranzo, Maria Àngels
Godoy‐Nieto, Cristina
López‐de‐Uralde‐Villanueva, Ibai
description ObjectiveTo evaluate the psychometric properties of the Spanish versions of the child‐ and parent‐report cystic fibrosis questionnaire‐revised (CFQ‐R).MethodsA 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.ResultsThe 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.ConclusionBoth 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.
doi_str_mv 10.1002/ppul.26671
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The CFQ‐R was completed twice, 7−10 days apart, and its psychometric properties were analyzed.ResultsThe internal consistency of both CFQ‐R versions was adequate (child‐report version, Cronbach's α &gt;.60 for all domains except “Treatment Burden” [α = .42] and “Social Functioning” [α = .57]; parent‐report version, α &gt; .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.ConclusionBoth 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.</description><identifier>ISSN: 8755-6863</identifier><identifier>EISSN: 1099-0496</identifier><identifier>DOI: 10.1002/ppul.26671</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Cystic fibrosis ; Quantitative psychology ; Questionnaires</subject><ispartof>Pediatric pulmonology, 2023-12, Vol.58 (12), p.3447-3457</ispartof><rights>2023. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c287t-43864e7db50ddb7cb3e865b00215b8c008d8e5d7b0abc832f2cbbeff9257c7aa3</cites><orcidid>0000-0002-7801-351X ; 0000-0002-5889-1841</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Blanco‐Orive, Paula</creatorcontrib><creatorcontrib>del Corral, Tamara</creatorcontrib><creatorcontrib>Martín‐Casas, Patricia</creatorcontrib><creatorcontrib>Cebrià I Iranzo, Maria Àngels</creatorcontrib><creatorcontrib>Godoy‐Nieto, Cristina</creatorcontrib><creatorcontrib>López‐de‐Uralde‐Villanueva, Ibai</creatorcontrib><title>Spanish adaptation and validation of the child‐ and parent‐report cystic fibrosis questionnaire‐revised (CFQ‐R)</title><title>Pediatric pulmonology</title><description>ObjectiveTo evaluate the psychometric properties of the Spanish versions of the child‐ and parent‐report cystic fibrosis questionnaire‐revised (CFQ‐R).MethodsA 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.ResultsThe internal consistency of both CFQ‐R versions was adequate (child‐report version, Cronbach's α &gt;.60 for all domains except “Treatment Burden” [α = .42] and “Social Functioning” [α = .57]; parent‐report version, α &gt; .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.ConclusionBoth 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.</description><subject>Cystic fibrosis</subject><subject>Quantitative psychology</subject><subject>Questionnaires</subject><issn>8755-6863</issn><issn>1099-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkc1KAzEUhYMoWKsbnyDgpgpTk5nmbynFqiCIf-shf0NTpjMxmal05yP4jD6J6dSVq8vhfPdyLgeAc4ymGKH82vu-nuaUMnwARhgJkaGZoIdgxBkhGeW0OAYnMa4QSp7AI_D56mXj4hJKI30nO9c2UDYGbmTtzF62FeyWFuqlq83P1_dgexls0yUVrG9DB_U2dk7DyqnQRhfhR2_jbrmRLtgB27hoDZzMF89JvlyegqNK1tGe_c0xeF_cvs3vs8enu4f5zWOmc866bFZwOrPMKIKMUUyrwnJKVHoVE8U1QtxwSwxTSCrNi7zKtVK2qkROmGZSFmMw2d_1oR1ClWsXta1r2di2j2We7lNMRS4SevEPXbV9aFK6RAksCKEFTtTVntLp0xhsVfrg1jJsS4zKXQflroNy6KD4BfuWf-E</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Blanco‐Orive, Paula</creator><creator>del Corral, Tamara</creator><creator>Martín‐Casas, Patricia</creator><creator>Cebrià I Iranzo, Maria Àngels</creator><creator>Godoy‐Nieto, Cristina</creator><creator>López‐de‐Uralde‐Villanueva, Ibai</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7801-351X</orcidid><orcidid>https://orcid.org/0000-0002-5889-1841</orcidid></search><sort><creationdate>20231201</creationdate><title>Spanish adaptation and validation of the child‐ and parent‐report cystic fibrosis questionnaire‐revised (CFQ‐R)</title><author>Blanco‐Orive, Paula ; del Corral, Tamara ; Martín‐Casas, Patricia ; Cebrià I Iranzo, Maria Àngels ; Godoy‐Nieto, Cristina ; López‐de‐Uralde‐Villanueva, Ibai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c287t-43864e7db50ddb7cb3e865b00215b8c008d8e5d7b0abc832f2cbbeff9257c7aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Cystic fibrosis</topic><topic>Quantitative psychology</topic><topic>Questionnaires</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Blanco‐Orive, Paula</creatorcontrib><creatorcontrib>del Corral, Tamara</creatorcontrib><creatorcontrib>Martín‐Casas, Patricia</creatorcontrib><creatorcontrib>Cebrià I Iranzo, Maria Àngels</creatorcontrib><creatorcontrib>Godoy‐Nieto, Cristina</creatorcontrib><creatorcontrib>López‐de‐Uralde‐Villanueva, Ibai</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric pulmonology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blanco‐Orive, Paula</au><au>del Corral, Tamara</au><au>Martín‐Casas, Patricia</au><au>Cebrià I Iranzo, Maria Àngels</au><au>Godoy‐Nieto, Cristina</au><au>López‐de‐Uralde‐Villanueva, Ibai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spanish adaptation and validation of the child‐ and parent‐report cystic fibrosis questionnaire‐revised (CFQ‐R)</atitle><jtitle>Pediatric pulmonology</jtitle><date>2023-12-01</date><risdate>2023</risdate><volume>58</volume><issue>12</issue><spage>3447</spage><epage>3457</epage><pages>3447-3457</pages><issn>8755-6863</issn><eissn>1099-0496</eissn><abstract>ObjectiveTo evaluate the psychometric properties of the Spanish versions of the child‐ and parent‐report cystic fibrosis questionnaire‐revised (CFQ‐R).MethodsA 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.ResultsThe internal consistency of both CFQ‐R versions was adequate (child‐report version, Cronbach's α &gt;.60 for all domains except “Treatment Burden” [α = .42] and “Social Functioning” [α = .57]; parent‐report version, α &gt; .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.ConclusionBoth 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.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ppul.26671</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-7801-351X</orcidid><orcidid>https://orcid.org/0000-0002-5889-1841</orcidid><oa>free_for_read</oa></addata></record>
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subjects Cystic fibrosis
Quantitative psychology
Questionnaires
title Spanish adaptation and validation of the child‐ and parent‐report cystic fibrosis questionnaire‐revised (CFQ‐R)
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