Literature DB >> 22383270

Determinants of the burden and positivity of family caregivers of terminally ill cancer patients in Korea.

Chang-Hae Park1, Dong Wook Shin, Jin Young Choi, Jina Kang, Young Ji Baek, Ha Na Mo, Mee-Sook Lee, Seon-Ju Park, Sang Min Park, Sohee Park.   

Abstract

OBJECTIVE: Caregivers may experience positive or negative feelings about their role. The study investigated the determinants of the burden and positivity of family caregivers of Korean terminal cancer patients.
METHODS: A multicenter cross-sectional survey was conducted with 139 family caregivers. Determinants of caregiver's burden and positivity were assessed by the Caregiver Reaction Assessment Scale and by three questions based on a previous study, respectively. Two separate hierarchical multiple regression models were used.
RESULTS: Each domain of the caregiver's burden and positivity was explained by different factors, with the total explained variance ranging between 14.4-33.6% and 2.6-18.3%, respectively. Caregivers who were unmarried, less educated, and/or had low incomes were more likely to be negatively affected, while those who shared caregiving responsibilities were less prone to negative consequences. Caregivers who were male, religious practitioners, and who perceived a higher burden of schedule disruptions were more likely to have a positive perception of their role, while those who perceived a lack of family support were less likely.
CONCLUSIONS: Our results highlight the importance of sharing the caregiving burden with the other family members. Organizing a family meeting can provide an opportunity for other family members to acknowledge the feelings and reactions of the primary caregivers, and can prompt the sharing of caregiving responsibilities.
Copyright © 2010 John Wiley & Sons, Ltd.

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Mesh:

Year:  2010        PMID: 22383270     DOI: 10.1002/pon.1893

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  13 in total

1.  Predictors of burden and quality of sleep among family caregivers of patients with cancer.

Authors:  Laila I Al-Daken; Muayyad M Ahmad
Journal:  Support Care Cancer       Date:  2018-05-26       Impact factor: 3.603

2.  Association between hope and burden reported by family caregivers of patients with advanced cancer.

Authors:  Inger Utne; Christine Miaskowski; Steven M Paul; Tone Rustøen
Journal:  Support Care Cancer       Date:  2013-04-27       Impact factor: 3.603

3.  Examining the role of subjective and objective burden in carer health-related quality of life: the case of colorectal cancer.

Authors:  Paul Hanly; Rebecca Maguire; Philip Hyland; Linda Sharp
Journal:  Support Care Cancer       Date:  2014-12-12       Impact factor: 3.603

4.  Modifiable factors associated with caregiver burden among family caregivers of terminally ill Korean cancer patients.

Authors:  Seok-Joon Yoon; Jong-Sung Kim; Jin-Gyu Jung; Sung-Soo Kim; Samyong Kim
Journal:  Support Care Cancer       Date:  2014-01-16       Impact factor: 3.603

5.  Preliminary study of themes of meaning and psychosocial service use among informal cancer caregivers.

Authors:  Allison J Applebaum; Carol J Farran; Allison M Marziliano; Anna R Pasternak; William Breitbart
Journal:  Palliat Support Care       Date:  2013-08-07

6.  Longitudinal changes and predictors of caregiving burden while providing end-of-life care for terminally ill cancer patients.

Authors:  Kwo C Lee; Wen-Cheng Chang; Wen-Chi Chou; Po-Jung Su; Chia-Hsun Hsieh; Jen-Shi Chen; Siew Tzuh Tang
Journal:  J Palliat Med       Date:  2013-04-04       Impact factor: 2.947

7.  Providing care to relatives with mental illness: reactions and distress among primary informal caregivers.

Authors:  Sherilyn Chang; Yunjue Zhang; Anitha Jeyagurunathan; Ying Wen Lau; Vathsala Sagayadevan; Siow Ann Chong; Mythily Subramaniam
Journal:  BMC Psychiatry       Date:  2016-03-25       Impact factor: 3.630

8.  Caregivers of cancer patients: what are their information-seeking behaviours and resource preferences?

Authors:  Gek Phin Chua; Quan Sing Ng; Hiang Khoon Tan; Whee Sze Ong
Journal:  Ecancermedicalscience       Date:  2020-07-10

9.  Returning to work after stroke: perspectives of employer stakeholders, a qualitative study.

Authors:  Carol Coole; Kathryn Radford; Mary Grant; Jane Terry
Journal:  J Occup Rehabil       Date:  2013-09

Review 10.  Psychometric properties of carer-reported outcome measures in palliative care: A systematic review.

Authors:  Charlotte T J Michels; Mary Boulton; Astrid Adams; Bee Wee; Michele Peters
Journal:  Palliat Med       Date:  2015-09-25       Impact factor: 4.762

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