• español
  • English
  • français
  • Deutsch
  • português (Brasil)
  • italiano
  • Contact Us
  • Send Feedback
    • español
    • English
    • français
    • Deutsch
    • português (Brasil)
    • italiano
    • español
    • English
    • français
    • Deutsch
    • português (Brasil)
    • italiano
    JavaScript is disabled for your browser. Some features of this site may not work without it.
    Gredos. Repositorio documental de la Universidad de SalamancaUniversidad de Salamanca
    Consorcio BUCLE Recolector

    Browse

    All of GredosCommunities and CollectionsBy Issue DateAuthorsSubjectsTitlesThis CollectionBy Issue DateAuthorsSubjectsTitles

    My Account

    LoginRegister

    Statistics

    View Usage Statistics
    Estadísticas totales de uso y lectura

    ENLACES Y ACCESOS

    Derechos de autorPolíticasGuías de autoarchivoFAQAdhesión USAL a la Declaración de BerlínProtocolo de depósito, modificación y retirada de documentos y datosSolicitud de depósito, modificación y retirada de documentos y datos

    COMPARTIR

    View Item 
    •   Gredos Home
    • Scientific Repository
    • Grupos de Investigación
    • NEUROQUALYFAM. Enfermedades Neurodegenerativas y Calidad de Vida Familiar
    • NEUROQUALYFAM. Ponencias / Actas
    • View Item
    •   Gredos Home
    • Scientific Repository
    • Grupos de Investigación
    • NEUROQUALYFAM. Enfermedades Neurodegenerativas y Calidad de Vida Familiar
    • NEUROQUALYFAM. Ponencias / Actas
    • View Item

    Compartir

    Exportar

    RISMendeleyRefworksZotero
    • edm
    • marc
    • xoai
    • qdc
    • ore
    • ese
    • dim
    • uketd_dc
    • oai_dc
    • etdms
    • rdf
    • mods
    • mets
    • didl
    • premis

    Citas

    Título
    Supports received by the families of people with neurodegenerative disease: a quantitative and qualitative approach
    Autor(es)
    Aza Hernández, AlbaUSAL authority ORCID
    Gómez Vela, MaríaUSAL authority ORCID
    González Ortega, EvaUSAL authority ORCID
    Vicario Molina, IsabelUSAL authority ORCID
    Orgaz Baz, María BegoñaUSAL authority ORCID
    Badia Corbella, MartaUSAL authority ORCID
    NEUROQUALYFAM group
    Palabras clave
    Neurodegenerative disease
    Families
    Focus Groups
    FQoLS-ND
    Services
    Fecha de publicación
    2021-11-01
    Editor
    Cambridge University Press
    Citación
    Aza, A., Gómez-Vela, M., González, E., Vicario-Molina, I., Orgaz, M., & Badia, M. (2021). 406 - Supports received by the families of people with neurodegenerative disease: A quantitative and qualitative approach. International Psychogeriatrics, 33(S1), 32-33. doi:10.1017/S1041610221001654
    Resumen
    Introduction: When neurodegenerative disease (ND) is diagnosed, the family’s quality of life (FQoL) changes drastically. Within the concept of FQoL, the supports they receive from others at the community level and from services is one of the most important issues. Nonetheless, studies available using a mixed-methods approach are still limited. Consequently, the objective was to study the domains of support from services and support from others (emotional and practical), through the application of a quantitative instrument and the conduction of focus groups. Method: Three hundred relatives of people with ND, recruited from Regional Health Management of Castille and 14 Leon (Spain) completed the instrument FQOLS–ND, a specific scale for measuring quality of life in families caring for people with a ND. The mean age of the sample is 62.4 years and the majority are females (70%). In addition, a focus group was carried out with 10 family members (70% females, mean age= 61.6) aiming at the analysis of the quality of life domains. Results: The domains support of others (emotional and practical) and support from services achieved low quantitative levels specially in terms of achievement (M emotional =3.30; SD emotional = 1.21; M practical = 3.09, SD practical = 1.26; M services = 2.83; SD services = 1.02;). In the focus group, the main topics mentioned as negatively affecting the FQoL were social isolation, access and correct follow-up in specialized care services, lack of information on the diagnosis and progression of ND and on the needs of the person, and lack of empathy of professionals and others. Conclusions: ND negatively and significantly affects the family as a whole. Despite this, the emotional and practical support they receive from both other community members and professionals and services is still very insufficient. Therefore, it is important to raise awareness of the needs of this population and to carry out transformations in the attention provided.
    URI
    https://hdl.handle.net/10366/148272
    ISSN
    1741-203X (Online)
    DOI
    10.1017/S1041610221001654
    Versión del editor
    https://doi.org/10.1017/S1041610221001654
    Collections
    • NEUROQUALYFAM. Ponencias / Actas [14]
    Show full item record
    Files in this item
    Nombre:
    406-supports-received-by-the-families-of-people-with-neurodegenerative-disease-a-quantitative-and-qualitative-approach.pdf
    Tamaño:
    235.0Kb
    Formato:
    Adobe PDF
    Thumbnail
    FilesOpen
     
    Universidad de Salamanca
    AVISO LEGAL Y POLÍTICA DE PRIVACIDAD
    2024 © UNIVERSIDAD DE SALAMANCA
     
    Universidad de Salamanca
    AVISO LEGAL Y POLÍTICA DE PRIVACIDAD
    2024 © UNIVERSIDAD DE SALAMANCA