Rotina, necessidades e suporte de famílias de crianças com síndrome de down

Detalhes bibliográficos
Autor(a) principal: Pavão, Michelle Roberta
Data de Publicação: 2019
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UFSCAR
Texto Completo: https://repositorio.ufscar.br/handle/ufscar/11102
Resumo: The families of children with disabilities may have necessities that need to be feed to allow quality interaction with their children. Based on the hypothesis that such necessities may be specific considering the child's age and disability, the present research aimed at: (a) to identify and to analyze the routine, necessities and families social support of children from 0 to 6 years with Down syndrome, and (b) to relate the socio-demographic variables, necessities and families social support of the children aged between 0 to 6 years with Down syndrome. It was participated in the study fifteen parents or guardians of children aged between 0 to 6 years with Down syndrome. The instruments used to collect the data were: (a) Brazil Criteria Questionnaire; (b) Survey on the family needs; (c) Survey of social support and (d) Semi-Structured interview script "Necessities, support and stimulation of families of children with disabilities" (which was prepared for this study). These instruments were applied in the form of interviews. Qualitative and quantitative data were obtained via the instruments. Qualitative data were analyzed via categories previously established in the interview script. Quantitative data were analyzed using descriptive methods (central tendency measures and dispersion). The Pearson's correlation coefficient was used to relate sociodemographic variables, necessities and families social support. The results showed that the greatest necessities of the families were related to the information about the child's disability and the support services that could assist in its development. In relation to the social support, the families were supportive to diverse situations. Considering the routine, most of the children had certain schedules to do the day-to-day activities, a therapies routine and intensive care and they was highly stimulated inside and outside the home. It was also noted that they had a diversity of toys and materials in the home. When correlating the necessities, social support and sociodemographic variables data, it was verified that: (a) the higher the participants' schooling, the greater the total social support; (b) the higher the number of siblings, the greater the support needs; (c) the older the children, the greater the need to explain to others; (d) the higher the per capita income of the family, the greater the total social support and the need to explain to others, and (e) the longer the age of the participants, the greater the need for community services, as well as correlating with the total necessities. It is concluded that this study specifically covered families of children with Down syndrome, and thus, it serves as a guide to possible interventions, considering the specificities of the age group and the target population.
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spelling Pavão, Michelle RobertaCia, Fabianahttp://lattes.cnpq.br/5999108571365402http://lattes.cnpq.br/34803486274511996255d6ca-224e-4f9e-9750-20cdf46d65a42019-03-19T21:33:04Z2019-03-19T21:33:04Z2019-02-20PAVÃO, Michelle Roberta. Rotina, necessidades e suporte de famílias de crianças com síndrome de down. 2019. Dissertação (Mestrado em Educação Especial) – Universidade Federal de São Carlos, São Carlos, 2019. Disponível em: https://repositorio.ufscar.br/handle/ufscar/11102.https://repositorio.ufscar.br/handle/ufscar/11102The families of children with disabilities may have necessities that need to be feed to allow quality interaction with their children. Based on the hypothesis that such necessities may be specific considering the child's age and disability, the present research aimed at: (a) to identify and to analyze the routine, necessities and families social support of children from 0 to 6 years with Down syndrome, and (b) to relate the socio-demographic variables, necessities and families social support of the children aged between 0 to 6 years with Down syndrome. It was participated in the study fifteen parents or guardians of children aged between 0 to 6 years with Down syndrome. The instruments used to collect the data were: (a) Brazil Criteria Questionnaire; (b) Survey on the family needs; (c) Survey of social support and (d) Semi-Structured interview script "Necessities, support and stimulation of families of children with disabilities" (which was prepared for this study). These instruments were applied in the form of interviews. Qualitative and quantitative data were obtained via the instruments. Qualitative data were analyzed via categories previously established in the interview script. Quantitative data were analyzed using descriptive methods (central tendency measures and dispersion). The Pearson's correlation coefficient was used to relate sociodemographic variables, necessities and families social support. The results showed that the greatest necessities of the families were related to the information about the child's disability and the support services that could assist in its development. In relation to the social support, the families were supportive to diverse situations. Considering the routine, most of the children had certain schedules to do the day-to-day activities, a therapies routine and intensive care and they was highly stimulated inside and outside the home. It was also noted that they had a diversity of toys and materials in the home. When correlating the necessities, social support and sociodemographic variables data, it was verified that: (a) the higher the participants' schooling, the greater the total social support; (b) the higher the number of siblings, the greater the support needs; (c) the older the children, the greater the need to explain to others; (d) the higher the per capita income of the family, the greater the total social support and the need to explain to others, and (e) the longer the age of the participants, the greater the need for community services, as well as correlating with the total necessities. It is concluded that this study specifically covered families of children with Down syndrome, and thus, it serves as a guide to possible interventions, considering the specificities of the age group and the target population.As famílias de crianças com deficiência podem ter necessidades que precisam ser supridas para permitir uma interação de qualidade com os filhos. Partindo da hipótese de que tais necessidades podem ser específicas, considerando a idade e a deficiência do filho, a presente pesquisa teve por objetivos: (a) identificar e analisar a rotina, as necessidades e o suporte social das famílias de crianças de 0 a 6 anos com síndrome de Down e (b) relacionar as variáveis sociodemográficas, as necessidades e o suporte social das famílias de crianças de 0 a 6 anos com síndrome de Down. Participaram da pesquisa 15 pais ou responsáveis de crianças com síndrome de Down, de zero a seis anos de idade. Os instrumentos utilizados para a coleta dos dados foram: (a) Questionário Critério Brasil; (b) Questionário sobre as necessidades das famílias-QNF; (c) Questionário de Suporte Social-SSQ e (d) Roteiro de entrevista semiestruturado “Necessidades, suporte e estimulação de famílias de crianças com deficiência” (que foi elaborado para esse estudo). Tais instrumentos foram aplicados em forma de entrevista. Por meio dos instrumentos foram obtidos dados qualitativos e quantitativos. Os dados qualitativos foram analisados por meio de categorias previamente estabelecidas no roteiro de entrevista. Os dados quantitativos foram analisados usando métodos descritivos (medidas de tendência central e dispersão). Para relacionar as variáveis sociodemográficos, as necessidades e o suporte social das famílias, foi utilizado o teste de correlação de Pearson. Os resultados mostraram que as maiores necessidades das famílias estavam relacionadas às informações sobre a deficiência da criança e os serviços de apoio que poderiam auxiliá-la em seu desenvolvimento. Em relação ao suporte social, as famílias se mostraram suportivas à diversas situações. Considerando a rotina, a maioria das crianças tinha horários certos para realizar as atividades do dia a dia, possuía uma rotina de terapias e atendimentos intensivos e era bastante estimulada dentro e fora de casa. Também se notou que possuíam uma diversidade de brinquedos e materiais dentro de casa. Ao correlacionar os dados das necessidades, suporte social e variáveis sociodemográficas, verificou-se que: (a) quanto maior a escolaridade dos participantes, maior era o suporte social total; (b) quanto maior o número de irmãos, maior era a necessidade de apoio; (c) quanto maior a idade das crianças, maior era a necessidade de explicar aos outros; (d) quanto maior a renda per capita da família, maior era a necessidade de explicar aos outros e o suporte social total e (e) quanto maior era a idade dos participantes maior era a necessidade de serviços da comunidade, além de correlacionar-se com as necessidades totais. Conclui-se que esse estudo abarcou especificamente famílias de crianças com síndrome de Down, sendo assim, o mesmo torna-se possível norteador para possíveis intervenções, considerando as especificidades da faixa etária e da população alvo.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)porUniversidade Federal de São CarlosCâmpus São CarlosPrograma de Pós-Graduação em Educação Especial - PPGEEsUFSCarEducação especialFamíliaSíndrome de downCriançasSpecial educationFamilyDown's syndromeChildrenCIENCIAS HUMANAS::EDUCACAORotina, necessidades e suporte de famílias de crianças com síndrome de downRoutine, necessities and families support of children with down syndromeinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisOnline600600cc758ed6-e9ed-4202-83f6-69fcf52ac9d3info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARORIGINALDissertação de Mestrado 2019 para publicação.pdfDissertação de Mestrado 2019 para publicação.pdfDissertação de mestradoapplication/pdf1132218https://repositorio.ufscar.br/bitstream/ufscar/11102/1/Disserta%c3%a7%c3%a3o%20de%20Mestrado%202019%20para%20publica%c3%a7%c3%a3o.pdf35b2b3bb1b7d1a4c44e85073e0effa47MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81957https://repositorio.ufscar.br/bitstream/ufscar/11102/4/license.txtae0398b6f8b235e40ad82cba6c50031dMD54TEXTDissertação de Mestrado 2019 para publicação.pdf.txtDissertação de Mestrado 2019 para publicação.pdf.txtExtracted texttext/plain210847https://repositorio.ufscar.br/bitstream/ufscar/11102/5/Disserta%c3%a7%c3%a3o%20de%20Mestrado%202019%20para%20publica%c3%a7%c3%a3o.pdf.txtabd6109ee703932c877f242be5625831MD55THUMBNAILDissertação de Mestrado 2019 para publicação.pdf.jpgDissertação de Mestrado 2019 para publicação.pdf.jpgIM Thumbnailimage/jpeg7420https://repositorio.ufscar.br/bitstream/ufscar/11102/6/Disserta%c3%a7%c3%a3o%20de%20Mestrado%202019%20para%20publica%c3%a7%c3%a3o.pdf.jpgda1379cbd74b4987a375e8c122591269MD56ufscar/111022023-09-18 18:31:21.008oai:repositorio.ufscar.br:ufscar/11102TElDRU7Dh0EgREUgRElTVFJJQlVJw4fDg08gTsODTy1FWENMVVNJVkEKCkNvbSBhIGFwcmVzZW50YcOnw6NvIGRlc3RhIGxpY2Vuw6dhLCB2b2PDqiAobyBhdXRvciAoZXMpIG91IG8gdGl0dWxhciBkb3MgZGlyZWl0b3MgZGUgYXV0b3IpIGNvbmNlZGUgw6AgVW5pdmVyc2lkYWRlCkZlZGVyYWwgZGUgU8OjbyBDYXJsb3MgbyBkaXJlaXRvIG7Do28tZXhjbHVzaXZvIGRlIHJlcHJvZHV6aXIsICB0cmFkdXppciAoY29uZm9ybWUgZGVmaW5pZG8gYWJhaXhvKSwgZS9vdQpkaXN0cmlidWlyIGEgc3VhIHRlc2Ugb3UgZGlzc2VydGHDp8OjbyAoaW5jbHVpbmRvIG8gcmVzdW1vKSBwb3IgdG9kbyBvIG11bmRvIG5vIGZvcm1hdG8gaW1wcmVzc28gZSBlbGV0csO0bmljbyBlCmVtIHF1YWxxdWVyIG1laW8sIGluY2x1aW5kbyBvcyBmb3JtYXRvcyDDoXVkaW8gb3UgdsOtZGVvLgoKVm9jw6ogY29uY29yZGEgcXVlIGEgVUZTQ2FyIHBvZGUsIHNlbSBhbHRlcmFyIG8gY29udGXDumRvLCB0cmFuc3BvciBhIHN1YSB0ZXNlIG91IGRpc3NlcnRhw6fDo28KcGFyYSBxdWFscXVlciBtZWlvIG91IGZvcm1hdG8gcGFyYSBmaW5zIGRlIHByZXNlcnZhw6fDo28uCgpWb2PDqiB0YW1iw6ltIGNvbmNvcmRhIHF1ZSBhIFVGU0NhciBwb2RlIG1hbnRlciBtYWlzIGRlIHVtYSBjw7NwaWEgYSBzdWEgdGVzZSBvdQpkaXNzZXJ0YcOnw6NvIHBhcmEgZmlucyBkZSBzZWd1cmFuw6dhLCBiYWNrLXVwIGUgcHJlc2VydmHDp8Ojby4KClZvY8OqIGRlY2xhcmEgcXVlIGEgc3VhIHRlc2Ugb3UgZGlzc2VydGHDp8OjbyDDqSBvcmlnaW5hbCBlIHF1ZSB2b2PDqiB0ZW0gbyBwb2RlciBkZSBjb25jZWRlciBvcyBkaXJlaXRvcyBjb250aWRvcwpuZXN0YSBsaWNlbsOnYS4gVm9jw6ogdGFtYsOpbSBkZWNsYXJhIHF1ZSBvIGRlcMOzc2l0byBkYSBzdWEgdGVzZSBvdSBkaXNzZXJ0YcOnw6NvIG7Do28sIHF1ZSBzZWphIGRlIHNldQpjb25oZWNpbWVudG8sIGluZnJpbmdlIGRpcmVpdG9zIGF1dG9yYWlzIGRlIG5pbmd1w6ltLgoKQ2FzbyBhIHN1YSB0ZXNlIG91IGRpc3NlcnRhw6fDo28gY29udGVuaGEgbWF0ZXJpYWwgcXVlIHZvY8OqIG7Do28gcG9zc3VpIGEgdGl0dWxhcmlkYWRlIGRvcyBkaXJlaXRvcyBhdXRvcmFpcywgdm9jw6oKZGVjbGFyYSBxdWUgb2J0ZXZlIGEgcGVybWlzc8OjbyBpcnJlc3RyaXRhIGRvIGRldGVudG9yIGRvcyBkaXJlaXRvcyBhdXRvcmFpcyBwYXJhIGNvbmNlZGVyIMOgIFVGU0NhcgpvcyBkaXJlaXRvcyBhcHJlc2VudGFkb3MgbmVzdGEgbGljZW7Dp2EsIGUgcXVlIGVzc2UgbWF0ZXJpYWwgZGUgcHJvcHJpZWRhZGUgZGUgdGVyY2Vpcm9zIGVzdMOhIGNsYXJhbWVudGUKaWRlbnRpZmljYWRvIGUgcmVjb25oZWNpZG8gbm8gdGV4dG8gb3Ugbm8gY29udGXDumRvIGRhIHRlc2Ugb3UgZGlzc2VydGHDp8OjbyBvcmEgZGVwb3NpdGFkYS4KCkNBU08gQSBURVNFIE9VIERJU1NFUlRBw4fDg08gT1JBIERFUE9TSVRBREEgVEVOSEEgU0lETyBSRVNVTFRBRE8gREUgVU0gUEFUUk9Dw41OSU8gT1UKQVBPSU8gREUgVU1BIEFHw4pOQ0lBIERFIEZPTUVOVE8gT1UgT1VUUk8gT1JHQU5JU01PIFFVRSBOw4NPIFNFSkEgQSBVRlNDYXIsClZPQ8OKIERFQ0xBUkEgUVVFIFJFU1BFSVRPVSBUT0RPUyBFIFFVQUlTUVVFUiBESVJFSVRPUyBERSBSRVZJU8ODTyBDT01PClRBTULDiU0gQVMgREVNQUlTIE9CUklHQcOHw5VFUyBFWElHSURBUyBQT1IgQ09OVFJBVE8gT1UgQUNPUkRPLgoKQSBVRlNDYXIgc2UgY29tcHJvbWV0ZSBhIGlkZW50aWZpY2FyIGNsYXJhbWVudGUgbyBzZXUgbm9tZSAocykgb3UgbyhzKSBub21lKHMpIGRvKHMpCmRldGVudG9yKGVzKSBkb3MgZGlyZWl0b3MgYXV0b3JhaXMgZGEgdGVzZSBvdSBkaXNzZXJ0YcOnw6NvLCBlIG7Do28gZmFyw6EgcXVhbHF1ZXIgYWx0ZXJhw6fDo28sIGFsw6ltIGRhcXVlbGFzCmNvbmNlZGlkYXMgcG9yIGVzdGEgbGljZW7Dp2EuCg==Repositório InstitucionalPUBhttps://repositorio.ufscar.br/oai/requestopendoar:43222023-09-18T18:31:21Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)false
dc.title.por.fl_str_mv Rotina, necessidades e suporte de famílias de crianças com síndrome de down
dc.title.alternative.eng.fl_str_mv Routine, necessities and families support of children with down syndrome
title Rotina, necessidades e suporte de famílias de crianças com síndrome de down
spellingShingle Rotina, necessidades e suporte de famílias de crianças com síndrome de down
Pavão, Michelle Roberta
Educação especial
Família
Síndrome de down
Crianças
Special education
Family
Down's syndrome
Children
CIENCIAS HUMANAS::EDUCACAO
title_short Rotina, necessidades e suporte de famílias de crianças com síndrome de down
title_full Rotina, necessidades e suporte de famílias de crianças com síndrome de down
title_fullStr Rotina, necessidades e suporte de famílias de crianças com síndrome de down
title_full_unstemmed Rotina, necessidades e suporte de famílias de crianças com síndrome de down
title_sort Rotina, necessidades e suporte de famílias de crianças com síndrome de down
author Pavão, Michelle Roberta
author_facet Pavão, Michelle Roberta
author_role author
dc.contributor.authorlattes.por.fl_str_mv http://lattes.cnpq.br/3480348627451199
dc.contributor.author.fl_str_mv Pavão, Michelle Roberta
dc.contributor.advisor1.fl_str_mv Cia, Fabiana
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/5999108571365402
dc.contributor.authorID.fl_str_mv 6255d6ca-224e-4f9e-9750-20cdf46d65a4
contributor_str_mv Cia, Fabiana
dc.subject.por.fl_str_mv Educação especial
Família
Síndrome de down
Crianças
topic Educação especial
Família
Síndrome de down
Crianças
Special education
Family
Down's syndrome
Children
CIENCIAS HUMANAS::EDUCACAO
dc.subject.eng.fl_str_mv Special education
Family
Down's syndrome
Children
dc.subject.cnpq.fl_str_mv CIENCIAS HUMANAS::EDUCACAO
description The families of children with disabilities may have necessities that need to be feed to allow quality interaction with their children. Based on the hypothesis that such necessities may be specific considering the child's age and disability, the present research aimed at: (a) to identify and to analyze the routine, necessities and families social support of children from 0 to 6 years with Down syndrome, and (b) to relate the socio-demographic variables, necessities and families social support of the children aged between 0 to 6 years with Down syndrome. It was participated in the study fifteen parents or guardians of children aged between 0 to 6 years with Down syndrome. The instruments used to collect the data were: (a) Brazil Criteria Questionnaire; (b) Survey on the family needs; (c) Survey of social support and (d) Semi-Structured interview script "Necessities, support and stimulation of families of children with disabilities" (which was prepared for this study). These instruments were applied in the form of interviews. Qualitative and quantitative data were obtained via the instruments. Qualitative data were analyzed via categories previously established in the interview script. Quantitative data were analyzed using descriptive methods (central tendency measures and dispersion). The Pearson's correlation coefficient was used to relate sociodemographic variables, necessities and families social support. The results showed that the greatest necessities of the families were related to the information about the child's disability and the support services that could assist in its development. In relation to the social support, the families were supportive to diverse situations. Considering the routine, most of the children had certain schedules to do the day-to-day activities, a therapies routine and intensive care and they was highly stimulated inside and outside the home. It was also noted that they had a diversity of toys and materials in the home. When correlating the necessities, social support and sociodemographic variables data, it was verified that: (a) the higher the participants' schooling, the greater the total social support; (b) the higher the number of siblings, the greater the support needs; (c) the older the children, the greater the need to explain to others; (d) the higher the per capita income of the family, the greater the total social support and the need to explain to others, and (e) the longer the age of the participants, the greater the need for community services, as well as correlating with the total necessities. It is concluded that this study specifically covered families of children with Down syndrome, and thus, it serves as a guide to possible interventions, considering the specificities of the age group and the target population.
publishDate 2019
dc.date.accessioned.fl_str_mv 2019-03-19T21:33:04Z
dc.date.available.fl_str_mv 2019-03-19T21:33:04Z
dc.date.issued.fl_str_mv 2019-02-20
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dc.identifier.citation.fl_str_mv PAVÃO, Michelle Roberta. Rotina, necessidades e suporte de famílias de crianças com síndrome de down. 2019. Dissertação (Mestrado em Educação Especial) – Universidade Federal de São Carlos, São Carlos, 2019. Disponível em: https://repositorio.ufscar.br/handle/ufscar/11102.
dc.identifier.uri.fl_str_mv https://repositorio.ufscar.br/handle/ufscar/11102
identifier_str_mv PAVÃO, Michelle Roberta. Rotina, necessidades e suporte de famílias de crianças com síndrome de down. 2019. Dissertação (Mestrado em Educação Especial) – Universidade Federal de São Carlos, São Carlos, 2019. Disponível em: https://repositorio.ufscar.br/handle/ufscar/11102.
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