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dc.contributor.authorJiménez García Tizón, Sara 
dc.contributor.authorNavarro-Prados, Ana Belén 
dc.contributor.authorBueno Martínez, María Belén 
dc.date.accessioned2025-03-21T07:07:24Z
dc.date.available2025-03-21T07:07:24Z
dc.date.issued2025-03-20
dc.identifier.citationJiménez García-Tizón, S., Navarro Prados, A. B., y Bueno Martínez, M. B. (2025). Towards a comprehensive psychosocial profile of the family caregiver of people with dementia: Guidelines for intervention. Psicologia: Reflexão e Crítica 38(6). https://doi.org/10.1186/s41155-025-00342-5es_ES
dc.identifier.urihttp://hdl.handle.net/10366/164380
dc.description.abstract[EN]Background The profile of caregivers focuses on socio-demographic variables (age, gender, kinship, and educational level). However, buffer variables (e.g., dysfunctional thoughts) and indicators of the impacts of caregiving (e.g., stress) are often overlooked. Objective The study aims to offer a comprehensive view of the profile of the family caregiver of people with dementia by considering aspects contemplated in theoretical explanatory models of care. Methods It was based on a cross-sectional design. Socio-demographic and care-related characteristics and variables of the consequences of caregiving and related buffers were evaluated for 40 family caregivers of people with dementia. The Short form of Social Problem-Solving Inventory-Revised (SPSI-R-25), the Leisure Time Satisfaction Survey (LTS), the Revised Scale for Caregiving Self-Efficacy (RSCSE), the Escala de Habilidades Sociales (EHS), the Psychosocial Support Questionnaire (PSQ), the Cuestionario de Pensamientos Disfuncionales (CPD), the Caregiver Burden Interview (CBI), the Center for Epidemiologic Studies-Depression Scale (CES-D), the Perceived Stress Scale (PSS) and the World Health Organization Quality of Life Assessment–AGE (WHOQOL-AGE) were utilized. Descriptions of the variables and contrast tests (chi-square tests, t-tests, and two-factor ANOVAs) were made and used to compare the differences according to gender and kinship. Results Family caregivers are women, typically around 60 years old, wives or daughters, married, with primary/secondary education, who spend long hours caring with little support. They presented a low level of social and problemsolving skills, received little social support, had low self-efficacy and quality of life, highly dysfunctional thoughts, overload, depressive symptomatology, and stress. Significant differences were found according to kinship in educational level, employment status, hours per day dedicated to care time, and contemplating placing the person in a nursing home. Significant differences by kinship were also found in self-efficacy for responding to disruptive behaviors, perceived social support, and stress. Spouses have lower levels of this type of self-efficacy and have higher levels of stress but perceive greater social support. Males have higher levels of dysfunctional thoughts. Conclusion This study facilitates the identification of the specific needs of caregivers, to provide them with individualized interventions. Spouses and offspring present different needs and therefore interventions should be different.es_ES
dc.language.isoenges_ES
dc.publisherSpringerOpenes_ES
dc.rightsAttribution-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nd/4.0/*
dc.subjectCarees_ES
dc.subjectDementiaes_ES
dc.subjectFamily caregiveres_ES
dc.subjectProfilees_ES
dc.subjectPsychoeducational interventiones_ES
dc.titleTowards a comprehensive psychosocial profile of the family caregiver of people with dementia: Guidelines for interventiones_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://prc.springeropen.com/articles/10.1186/s41155-025-00342-5es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.journal.titlePsicologia: Reflexão e Críticaes_ES
dc.volume.number38es_ES
dc.issue.number6es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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