Determination of Caregiver Burden and Social Support Levels among Caregivers Providing Care for Patients Hospitalized in Palliative Care Clinics

ArticleAçık Erişim

Özet

Providing care to someone with a chronic disease requires being physically, emotionally, and mentally energetic. In particular, the presence of a patient with a disease that requires palliative care changes daily activities and routines, increases responsibilities of those who take the responsibility for patient's care and changes the roles in the family. The objective of this study was to determine the care burden and social support levels among the caregivers providing care for patients hospitalized in palliative care clinics. Materials and Methods. The population of this descriptive and correlational study consisted of caregivers taking care of patients treated at the Palliative Care Clinic of Training and Research Hospital between May and October 2018; the sample consisted of 73 caregivers who volunteered to join the study and were open to communication. Data were collected by questioning patients and their caregivers about their sociodemographic characteristics, using the Caregiver Burden Scale and the Multidimensional Scale of Perceived Social Support. Data analysis included percentages, the Kruskal-Wallis test, the Mann-Whitney U test, and the Spearman's Correlation Coefficient. Results. The average caregivers' age was 45.44 +/- 13.76 years; 75.3% of caregivers were females, 30.1% of caregivers were literate or had primary school degrees. Caregiver's gender and educational levels were found not to affect caregiving and social support levels; however, the economic status affected caregiving and social support levels. There was a reverse correlation between the caregiver burden and their social support levels. Conclusions. With increased caregiver burden, their social support level decreased. Nurses caring for patients in palliative care clinics will benefit from educating and supporting caregivers about clinic and home care; it will result in a positive level of social support for both caregivers and patients receiving care.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/16761Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.21802/gmj.2020.4.14Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorKarakurt, Papatya
dc.contributor.authorTuncer, Sevinc Kose
dc.contributor.authorCiltas, Nadire Yildiz
dc.contributor.authorDogan, Mehmet
dc.date.accessioned2026-10-18T20:38:52.046901745Z
dc.date.available2026-10-18T20:38:52.046901745Z
dc.date.issued2020
dc.description.abstractProviding care to someone with a chronic disease requires being physically, emotionally, and mentally energetic. In particular, the presence of a patient with a disease that requires palliative care changes daily activities and routines, increases responsibilities of those who take the responsibility for patient's care and changes the roles in the family. The objective of this study was to determine the care burden and social support levels among the caregivers providing care for patients hospitalized in palliative care clinics. Materials and Methods. The population of this descriptive and correlational study consisted of caregivers taking care of patients treated at the Palliative Care Clinic of Training and Research Hospital between May and October 2018; the sample consisted of 73 caregivers who volunteered to join the study and were open to communication. Data were collected by questioning patients and their caregivers about their sociodemographic characteristics, using the Caregiver Burden Scale and the Multidimensional Scale of Perceived Social Support. Data analysis included percentages, the Kruskal-Wallis test, the Mann-Whitney U test, and the Spearman's Correlation Coefficient. Results. The average caregivers' age was 45.44 +/- 13.76 years; 75.3% of caregivers were females, 30.1% of caregivers were literate or had primary school degrees. Caregiver's gender and educational levels were found not to affect caregiving and social support levels; however, the economic status affected caregiving and social support levels. There was a reverse correlation between the caregiver burden and their social support levels. Conclusions. With increased caregiver burden, their social support level decreased. Nurses caring for patients in palliative care clinics will benefit from educating and supporting caregivers about clinic and home care; it will result in a positive level of social support for both caregivers and patients receiving care.
dc.identifier.doi10.21802/gmj.2020.4.14
dc.identifier.eissn2414-1518
dc.identifier.issn2306-4285
dc.identifier.issue4
dc.identifier.startpageE2020414
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/16761
dc.identifier.volume27
dc.identifier.wosWOS:000827697200010
dc.language.isoen
dc.publisherIVANO-FRANKIVSK NATL MEDICAL UNIV
dc.relation.ispartofGALICIAN MEDICAL JOURNAL
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCaregivers
dc.subjectCare Burden
dc.subjectPalliative Care
dc.subjectSocial Support
dc.subjectNursing
dc.subjectMULTIDIMENSIONAL SCALE
dc.subjectMedicine, General & Internal
dc.subjectGeneral & Internal Medicine
dc.titleDetermination of Caregiver Burden and Social Support Levels among Caregivers Providing Care for Patients Hospitalized in Palliative Care Clinics
dc.typeArticle
dspace.entity.typePublication
rdl.citation.wos6
rdl.oa.statusgold
rdl.source.indexWOS
rdl.wos.indexEmerging Sources Citation Index (ESCI)