Please use this identifier to cite or link to this item: http://hdl.handle.net/11144/4505
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dc.contributor.authorBrites, Rute-
dc.contributor.authorBrandão, Tânia-
dc.contributor.authorPereira, Francisco M-
dc.contributor.authorHipólito, João-
dc.contributor.authorNunes, Odete-
dc.date.accessioned2020-03-11T11:53:55Z-
dc.date.available2020-03-11T11:53:55Z-
dc.date.issued2020-01-
dc.identifier.issn1744-6163-
dc.identifier.urihttp://hdl.handle.net/11144/4505-
dc.description.abstractPurpose: This study aimed to examine the factors associated with the development of higher burden in informal care-givers of patients with dementia, using dyadic data. Design and Methods: Seventy-two dyads of patients with dementia and their informal care-givers were assessed, the former in terms of behavioral-psychological symptoms and autonomy, the latter in terms of burden and individual needs. Findings: Care-givers at risk for developing higher burden are those who are female, whose care recipient present psychiatric symptoms and lower autonomy, and those who recognize the need for more information/support. Practice Implications: Interventions should offer care-givers the tools to provide care, maintaining their psychological well-being. Interventions should target not only common aspects of care-giver burden but also the specificities of caring for a person with dementia.pt_PT
dc.language.isoengpt_PT
dc.publisherWileypt_PT
dc.rightsopenAccesspt_PT
dc.subjectInformal care-giverspt_PT
dc.subjectburdenpt_PT
dc.subjectdementiapt_PT
dc.subjectbehavioral symptomspt_PT
dc.subjectautonomypt_PT
dc.titleEffects of supporting patients with dementia: A study with dyadspt_PT
dc.typearticlept_PT
degois.publication.titlePerspectives in Psychiatric Carept_PT
dc.peerreviewedyespt_PT
dc.identifier.doi10.1111/ppc.12476pt_PT
Appears in Collections:CIP - Artigos/Papers

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