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Family Caregiver’s Depression, Confidence, Satisfaction, and Burden Regarding End-of-Life Home Care for People With End-Stage Dementia

Dados Bibliográficos

ID13629638
AutoresGary Green (0000-0002-3649-2145, Ariel University, autor correspondente), Inbal Halevi Hochwald (0000-0002-4930-2072, Nursing Department, Max Stern Yezreel Valley, Emek Yezreel, Israel), Zorian Radomyslsky (0000-0003-2410-6726, Maccabi Healthcare Services, Tel-Aviv, Israel), Rachel Nissanholtz‐Gannot (0000-0003-4014-2874, Ariel University), Rachel Nissanholtz-Gannot (Ariel University)
Ano2022
Volume91
Fascículo2
Páginas1041-1057
Data de publicação2022-12-27
Peer ReviewedSim
Open AccessSim
TipoARTICLE
PeriódicoOMEGA - Journal of Death and Dying (JOURNAL)
Identificadores do periódicoISSN: 0030-2228 • E-ISSN: 1541-3764
EditoraSAGE Publishing (PUBLISHER • US)
DOI10.1177/00302228221147961
PMID36573833
OpenAlexW4312212022
IdiomaEN
Citações recebidas2
Referências citadas50

To detect differences between two care services units: regarding family-caregiver (FC) depression, perceived-burden and confidence in the provision of care to people with end-stage dementia (PWESD); examine predictors such as FC age, depression, confidence in the provision of care to PWESD and satisfaction with the community-home-care service to burden; and explore a mediation model.The participants were 139 FC, caring for PWESD living at home. The questionnaire was composed of FC background characteristics, perceived-burden, satisfaction with the community-home-care services, depression, and confidence in the provision of care to the PWESD. HCUs' FC felt significantly more burdened than HHUs' FC. Furthermore, satisfaction with the community-home-care services mediated the relationship between FC confidence in the provision of care to the PWESD and FC burden. The study results may affect the development of end-of-life care policies and services which meet the needs of PWESD and their FC

Affect (linguistics · Caregiver burden · Dementia · Depression (economics · Disease · End-of-life care · Family caregivers · Mediation · Palliative care · Dementia and Cognitive Impairment Research · Geriatric Care and Nursing Homes · Medicine · Nursing · Palliative Care and End-of-Life Issues · Psychology · Gerontology

  • Agencies Displayed by Patients, Medical Teams, and Caregivers at the End of Life from the Perspectives of Family Members – A Qualitative Study

    Open Access•Yoel Tawil, Moran Bodas et al.•OMEGA - Journal of Death and Dying•2023

  • Vulnerabilities in migrant live-in care arrangements for people with dementia

    Open Access•Natalie Ulitsa, Anna Eva Nebowsky et al.•Frontiers in Psychiatry•2025

  • Caregiver burden for informal caregivers of patients with dementia

    Open Access•C-Y Chiao, H-S Wu et al.•International Nursing Review•2015

  • Screening for Depression in Well Older Adults

    Open Access•Elena M Andresen, Judith A Malmgren et al.•American Journal of Preventive…•1994

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    Steven H Zarit, Karen E Reever et al.•The Gerontologist•1980

  • Family Decision‐Making for Nursing Home Residents With Dementia

    Open Access•Charles E Gessert, Barbara A Elliott et al.•The Journal of Rural Health•2006

  • Level of Burden and Health-Related Quality of Life in Caregivers of Palliative Care Patients

    Open Access•Juana Perpiñá-Galvañ, Juana Perpiñá‐galvañ et al.•International Journal of…•2019

  • Social isolation, loneliness and health in old age

    Open Access•Emilie Courtin, Mel Knapp et al.•Health & Social Care in the…•2017

  • Challenges in home care at the end stage of dementia

    Inbal Halevi Hochwald, Zorian Radomyslsky et al.•Death Studies•2020

Obras citantes distintas2
Citações por ano0,67
Intervalo de citações2023 - 2025 (3)
Velocidade de citaçãorecent
Altamente citadoNão
Tipos de citaçãoNeutras: 2
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