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dc.contributor.authorSánchez Gómez, María Cruz 
dc.contributor.authorMartín-Sevillano, Rocío
dc.contributor.authorMartín Cilleros, María Victoria 
dc.contributor.authorMena Marcos, Juan José 
dc.contributor.authorGarcía Peñalvo, Francisco J. 
dc.date.accessioned2024-01-30T09:45:07Z
dc.date.available2024-01-30T09:45:07Z
dc.date.issued2021-09-13
dc.identifier.citationSánchez-Gómez, M. C., Martín-Sevillano, R., Martín-Cilleros, M. V., Marcos, J. J. M. y García-Peñalvo, F. J. (2021). Nurturing Grandchildren with Down Syndrome: A Qualitative Study on Grandparents’ Needs Using Digital Tools. Frontiers in Psychology, 12, 661205es_ES
dc.identifier.urihttp://hdl.handle.net/10366/154996
dc.description.abstract[EN]Grandparents who have grandchildren with disabilities are an underrepresented group in existing research related to the field. This qualitative phenomenological study’s general purpose is to analyze, from a personal perspective, the situations and needs of grandparents who have grandchildren with Down syndrome. The participants’ ages range from 65 to 85, and the ages of their grandchildren with Down syndrome range from 3 to 21 years. All participants had one grandchild with a disability, except for two, who each had two. A sociodemographic questionnaire was administered, and individual interviews were conducted, using open questions, through phone and/or video calls. An analysis of the participants’ speech was carried out, which implied the development of a system of meta-categories and categories. This analysis was developed manually, given the COVID-19 environment. The results indicate a substantial change from negative feelings caused by the knowledge of the diagnosis to feelings related to positive experiences expressed currently. The participants see themselves as a fundamental source of support (informal, instrumental, practical, social, emotional, and economic) for their families and, mainly, for their grandchildren with Down syndrome. A need for information and training was observed when the grandparents talked about first being informed of the diagnosis and their concerns about the future of these grandchildren and their siblings. They made social demands, such as greater government involvement or more significant opportunities to access resources and rights for their grandchildren. The results are discussed, as are possible future research directionses_ES
dc.description.sponsorshipEuropean Commissiones_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.publisherFrontierses_ES
dc.rightsAtribución-NoComercial 4.0 Internacional*
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectGrandparentses_ES
dc.subjectDown syndromees_ES
dc.subjectGrandchildrenes_ES
dc.subjectNeedses_ES
dc.subjectFamilyes_ES
dc.subjectQualitative investigationes_ES
dc.titleNurturing Grandchildren With Down Syndrome: A Qualitative Study on Grandparents’ Needs Using Digital Toolses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.3389/fpsyg.2021.661205
dc.subject.unesco6310.09 Calidad de Vidaes_ES
dc.identifier.doi10.3389/fpsyg.2021.661205
dc.relation.projectID2018-1-IT02-KA203-048402es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1664-1078
dc.journal.titleFrontiers in Psychologyes_ES
dc.volume.number12es_ES
dc.page.initial661205es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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