Effects of a short educational program about aphasia (SEPA) on the burden and quality of life of family caregivers of people with aphasia

Detalhes bibliográficos
Autor(a) principal: Magnus,Bruna Homem
Data de Publicação: 2019
Outros Autores: Dias,Roberta Freitas, Beber,Bárbara Costa
Tipo de documento: Relatório
Idioma: eng
Título da fonte: CoDAS
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2317-17822019000400501
Resumo: ABSTRACT Purpose To develop a short educational program about aphasia (SEPA) for family caregivers of people with aphasia and verify its effect in their burden and quality of life. Methods This is a quantitative experimental study. The participants included in the study were family caregivers of people with aphasia. They completed the Zarit interview scale and WHOQOL-Bref instruments pre- and post-intervention. The intervention was a short educational program about aphasia, administered in a group setting and conducted in two didactic sessions. Results Four participants were included in the study. In the group analysis, there was no significant difference in any measure. However, looking into the individual performances, all participants presented a trend for improvement in most of the scores. Conclusion Possibly, family caregivers of people with aphasia might benefit from the SEPA. It would be relevant for future studies to include larger samples and consider new strategies to improve inclusion of participants.
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spelling Effects of a short educational program about aphasia (SEPA) on the burden and quality of life of family caregivers of people with aphasiaAphasiaCaregiversSpeech, Language and Hearing SciencesEducationRehabilitationABSTRACT Purpose To develop a short educational program about aphasia (SEPA) for family caregivers of people with aphasia and verify its effect in their burden and quality of life. Methods This is a quantitative experimental study. The participants included in the study were family caregivers of people with aphasia. They completed the Zarit interview scale and WHOQOL-Bref instruments pre- and post-intervention. The intervention was a short educational program about aphasia, administered in a group setting and conducted in two didactic sessions. Results Four participants were included in the study. In the group analysis, there was no significant difference in any measure. However, looking into the individual performances, all participants presented a trend for improvement in most of the scores. Conclusion Possibly, family caregivers of people with aphasia might benefit from the SEPA. It would be relevant for future studies to include larger samples and consider new strategies to improve inclusion of participants.Sociedade Brasileira de Fonoaudiologia2019-01-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S2317-17822019000400501CoDAS v.31 n.4 2019reponame:CoDASinstname:Sociedade Brasileira de Fonoaudiologia (SBFA)instacron:SBFA10.1590/2317-1782/20192018218info:eu-repo/semantics/openAccessMagnus,Bruna HomemDias,Roberta FreitasBeber,Bárbara Costaeng2019-08-30T00:00:00Zoai:scielo:S2317-17822019000400501Revistahttps://www.codas.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.phpcodas@editoracubo.com.br||revista@codas.org.br2317-17822317-1782opendoar:2019-08-30T00:00CoDAS - Sociedade Brasileira de Fonoaudiologia (SBFA)false
dc.title.none.fl_str_mv Effects of a short educational program about aphasia (SEPA) on the burden and quality of life of family caregivers of people with aphasia
title Effects of a short educational program about aphasia (SEPA) on the burden and quality of life of family caregivers of people with aphasia
spellingShingle Effects of a short educational program about aphasia (SEPA) on the burden and quality of life of family caregivers of people with aphasia
Magnus,Bruna Homem
Aphasia
Caregivers
Speech, Language and Hearing Sciences
Education
Rehabilitation
title_short Effects of a short educational program about aphasia (SEPA) on the burden and quality of life of family caregivers of people with aphasia
title_full Effects of a short educational program about aphasia (SEPA) on the burden and quality of life of family caregivers of people with aphasia
title_fullStr Effects of a short educational program about aphasia (SEPA) on the burden and quality of life of family caregivers of people with aphasia
title_full_unstemmed Effects of a short educational program about aphasia (SEPA) on the burden and quality of life of family caregivers of people with aphasia
title_sort Effects of a short educational program about aphasia (SEPA) on the burden and quality of life of family caregivers of people with aphasia
author Magnus,Bruna Homem
author_facet Magnus,Bruna Homem
Dias,Roberta Freitas
Beber,Bárbara Costa
author_role author
author2 Dias,Roberta Freitas
Beber,Bárbara Costa
author2_role author
author
dc.contributor.author.fl_str_mv Magnus,Bruna Homem
Dias,Roberta Freitas
Beber,Bárbara Costa
dc.subject.por.fl_str_mv Aphasia
Caregivers
Speech, Language and Hearing Sciences
Education
Rehabilitation
topic Aphasia
Caregivers
Speech, Language and Hearing Sciences
Education
Rehabilitation
description ABSTRACT Purpose To develop a short educational program about aphasia (SEPA) for family caregivers of people with aphasia and verify its effect in their burden and quality of life. Methods This is a quantitative experimental study. The participants included in the study were family caregivers of people with aphasia. They completed the Zarit interview scale and WHOQOL-Bref instruments pre- and post-intervention. The intervention was a short educational program about aphasia, administered in a group setting and conducted in two didactic sessions. Results Four participants were included in the study. In the group analysis, there was no significant difference in any measure. However, looking into the individual performances, all participants presented a trend for improvement in most of the scores. Conclusion Possibly, family caregivers of people with aphasia might benefit from the SEPA. It would be relevant for future studies to include larger samples and consider new strategies to improve inclusion of participants.
publishDate 2019
dc.date.none.fl_str_mv 2019-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2317-17822019000400501
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2317-17822019000400501
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/2317-1782/20192018218
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Fonoaudiologia
publisher.none.fl_str_mv Sociedade Brasileira de Fonoaudiologia
dc.source.none.fl_str_mv CoDAS v.31 n.4 2019
reponame:CoDAS
instname:Sociedade Brasileira de Fonoaudiologia (SBFA)
instacron:SBFA
instname_str Sociedade Brasileira de Fonoaudiologia (SBFA)
instacron_str SBFA
institution SBFA
reponame_str CoDAS
collection CoDAS
repository.name.fl_str_mv CoDAS - Sociedade Brasileira de Fonoaudiologia (SBFA)
repository.mail.fl_str_mv codas@editoracubo.com.br||revista@codas.org.br
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