Care Burden and Quality of Life in Family Caregivers of Palliative Care Patients

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dc.authoridTuran, Mensure/0000-0002-1011-4963
dc.authoridCENGİZ, ZELİHA/0000-0002-3819-1717
dc.authorwosidTuran, Mensure/ISB-6773-2023
dc.authorwosidCENGİZ, ZELİHA/ABI-4480-2020
dc.contributor.authorCengiz, Zeliha
dc.contributor.authorTuran, Mensure
dc.contributor.authorOlmaz, Dilek
dc.contributor.authorErce, Cigdem
dc.date.accessioned2024-08-04T20:49:23Z
dc.date.available2024-08-04T20:49:23Z
dc.date.issued2021
dc.departmentİnönü Üniversitesien_US
dc.description.abstractThis research was conducted for the purpose of examining the care burden and quality of life in family caregivers of palliative care patients. The research design was a descriptive correlational study conducted with the caregivers of 163 patients residing in palliative care units. Data were collected via a demographic survey, The Zarit Burden Interview (ZBI) and the World Health Organization Quality of Life Assessment (WHOQOL). The results showed that there was a negative correlation between ZBI and WHOQOL scores. Further, there was a significant negative correlation between many subdimensions of the ZBI (general quality of life, general perception of health, being satisfied with daily life skills, home conditions, energy and self-satisfaction) and the WHOQOL. Quality of life thus appeared to be reduced in family members with a high level of care burden and that the quality of life of caregivers depends on the individual characteristics of the caregiver. Social workers, nurses and physicians should regularly assess the burden and quality of life of caregivers.en_US
dc.identifier.doi10.1080/15524256.2021.1888844
dc.identifier.endpage63en_US
dc.identifier.issn1552-4256
dc.identifier.issn1552-4264
dc.identifier.issue1en_US
dc.identifier.pmid33691608en_US
dc.identifier.scopus2-s2.0-85102563025en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage50en_US
dc.identifier.urihttps://doi.org/10.1080/15524256.2021.1888844
dc.identifier.urihttps://hdl.handle.net/11616/99817
dc.identifier.volume17en_US
dc.identifier.wosWOS:000628918300001en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherRoutledge Journals, Taylor & Francis Ltden_US
dc.relation.ispartofJournal of Social Work in End-Of-Life & Palliative Careen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCare burdenen_US
dc.subjectfamily caregiversen_US
dc.subjectpalliative careen_US
dc.subjectquality of lifeen_US
dc.titleCare Burden and Quality of Life in Family Caregivers of Palliative Care Patientsen_US
dc.typeArticleen_US

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