729
Views
28
CrossRef citations to date
0
Altmetric
Original Article

Relationship between caregiving burden and depression in caregivers of individuals with intellectual disabilities in Korea

&
Pages 50-56 | Received 16 Jun 2016, Accepted 11 Nov 2016, Published online: 13 Jan 2017

References

  • Agrell B, Dehlin O. (1989). Comparison of six depression rating scales in geriatric stroke patients. Stroke, 20, 1190–4.
  • Baik YW, Choi SI. (2010). Research about stress of a family caregiver who supports elderly for a long-term care. J Welfare Aged Inst, 49, 215–39.
  • Blacher J, Lopez S. (1997). Contributions to depression in Latina mothers with and without children with retardation: implications for care-giving. Fam Relat, 46, 325–34.
  • Buhse M. (2008). Assessment of caregiver burden in families of persons with multiple sclerosis. J Neurosci Nurs, 40, 25–31.
  • Bull M. (1990). Factors influencing caregiver burden and health. West J Nurs Res, 23, 756–76.
  • Burgener S, Twigg P. (2002). Relationships among caregiver factors and quality of life in care recipients with irreversible dementia. Alzheimer Dis Assoc Disord, 16, 88–102.
  • Carretero S, Garces J, Rodenas F, Sanjose V. (2009). The informal caregiver’s burden of dependent people: theory and empirical review. Arch Gerontol Geriatr, 49, 74–9.
  • Cho NO. (1996). A study of the dementia patient’s family experience and their nursing needs [dissertation]. Seoul (South Korea): Seoul National University.
  • Clyburn LD, Stone MJ, Hadjistavropoulos T. (2000). Predicting caregiver burden and depression in Alzheimer’s disease. J Gerontol Ser B, 55, 2–13.
  • Davis NO, Carter AS. (2008). Parenting stress in mothers and fathers of toddlers with autism spectrum disorders: Associations with child characteristics. J Aut Develop Disord, 38, 1278–91.
  • Etters L, Goodall D, Harrison BE. (2008). Caregiver burden among dementia patient caregivers: A review of the literature. J Am Acad Nurse Practit, 20, 423–8.
  • Gellis ZD. (2010). Assessment of a brief CES-D measure for depression in homebound medically ill older adults. J Gerontol Soc Work, 53, 289–303.
  • Grayson DA, Mackinnon A, Jorm AF, et al. (2000). Item bias in the center for epidemiologic studies depression scale effects of physical disorders and disability in an elderly community sample. J Gerontol Ser B, 55, 273–82.
  • Grzywacz JG, Hovey JD, Seligman LD, et al. (2006). Evaluating short-form versions of the CES-D for measuring depressive symptoms among immigrants from Mexico. Hispanic J Behav Sci, 28, 404–24.
  • Hann D, Winter K, Jacobsen P. (1999). Measurement of depressive symptoms in cancer patients: Evaluation of the Center for Epidemiological Studies Depression Scale (CES-D). J Psychosom Res, 46, 437–43.
  • Ingersoll D, Raschock M. (1996). The relationship between care-recipient behaviors and spousal caregiving stress. Gerontologist, 44, 318–27.
  • Kim H, Youn G. (1996). A comparative study on psychological burden between the demented and the nondemented elderly persons’ caregivers. Korea J Res Gerontol, 5, 107–29.
  • King G, King S, Rosenbaum P, Goffin R. (1999). Family-centered caregiving and well-being of parents of children with disabilities: linking process with outcome. J Pediatr Psychol, 24, 41–53.
  • Kosberg J, Cairl R. (1986). The cost of care index: a case management tool for screening informal care providers. Gerontologist, 26, 273–7.
  • Kwon JD. (1995). A study in the assessment of caregiver burden in caring for the demented elderly in Korea [dissertation]. Seoul (South Korea): Yeonsei University.
  • Lai DW. (2012). Effect of financial costs on caregiving burden of family caregivers of older adults. SAGE Open, 2, 1–14.
  • Lee AS, Kim HK. (2003). Care-givers’ attitude & determinants about the burden of the caring for dementia patients. Health Soc Sci, 13, 29–60.
  • Lee HS. (2012). Caregiver burden in caring for elders before and after long-term care service on Korea. J Korea Acad Nurs, 42, 236–47.
  • Lee SS. (1994). A study on caregiving burden of married women [dissertation]. Seoul (South Korea): Hanyang University
  • Lee YH, Kom HS, Cho IS. (2008). Factors influencing care burdens of caregivers ofelders with dementia who request dementia domiciliary welfare services. J Acad Fundamental Nurs, 15, 274–83.
  • Lee YW, Park K. (2007). A study on the influencing factors of dementia caregivers’s life satisfaction. J Nurs Query, 16, 135–56.
  • Lehmann V, Makine C, Karşıdağ Ç, et al. (2011). Validation of the Turkish version of the Centre for Epidemiologic Studies Depression Scale (CES-D) in patients with Type 2 diabetes mellitus. BMC Med Res Methodol, 11, 109.
  • Maanse H, Byung-Sun P, Sung-Woo B. (2015). Testing measurement invariance of the 11-item Korean version CES-D scale. Mental Health Soc Work, 43, 313–39.
  • Magaña SM, García JIR, Hernández MG, Cortez R. (2007). Psychological distress among Latino family caregivers of adults with schizophrenia: The roles of burden and stigma. Psychiatr Serv, 58, 378–84.
  • Manskow US, Sigurdardottir S, Røe C, et al. (2015). Factors affecting caregiver burden 1 year after severe traumatic brain injury: A prospective nationwide multicenter study. J Head Trauma Rehabilit, 30, 411–23.
  • Meyers JL, Gray LN. (2001). The relationships between family primary caregiver characteristics and satisfaction with hospice care, quality of life, and burden. Oncol Nurs Forum, 28, 73–82.
  • Molyneux GJ, McCarthy GM, McEniff S, et al. (2008). Prevalence and predictors of care burden and depression in careers of patients referred to an old age psychiatric service. Int Psychogeriatr, 20, 1193–202.
  • Montgomery R, Gonyea J, Hooyman N. (1985). Caregiving and experience of subjective and objective burden. Fam Relat, 34, 19–26.
  • Morris LW, Morris RG, Britton PG. (1988). The relationship between marital intimacy, perceived strain and depression in spouse caregivers of dementia sufferers. Br J Med Psychol, 61, 231–6.
  • Novak M, Guest C. (1989). Application of a multidimensional caregiver burden inventory. Gerontologist, 29, 798–803.
  • Papadtavrou E, Kalokerinou A, Papacostas SS, et al. (2007). Caring for a relative with dementia: family caregiver burden. J Adv Nurs, 58, 446–57.
  • Park C, Kim KT. (2003). Informal caregiving decision among caregivers to the severely disabled elderly and their resulting economic cost. J Welfare Aged, 20, 179–211.
  • Parks SM, Novielli KD. (2000). A practical guide to caring for caregivers. Am Fam Physician, 62, 2613–22.
  • Phipps S, Dunavant M, Lensing S, Rai SN. (2005). Psychosocial predictors of distress in parents of children undergoing stem cell or bone marrow transplantation. J Pediatr Psychol, 30, 139–53.
  • Pinquart M, Sörensen S. (2003). Differences between caregivers and noncaregivers in psychological health and physical health: A meta-analysis. Psychol Aging, 18, 250–67.
  • Pinquart M, Sörensen S. (2007). Correlates of physical health of informal caregivers: A meta-analysis. J Gerontol Ser B, 62, 126–37.
  • Raina P, O'Donnell M, Schwellnus H, et al. (2004). Caregiving process and caregiver burden: conceptual models to guide research and practice. BMC Pediatr, 4, 1.
  • Sawyer MG, Bittman M, La Greca AM, et al. (2011). Time demands of caring for children with cerebral palsy: what are the implications for maternal mental health? Develop Med Child Neurol, 53, 338–43.
  • Schulz R, O'Brien AT, Bookwala J, Fleissner K. (1995). Psychiatric and physical morbidity effects of dementia caregiving: Prevalence, correlates, and causes. Gerontologist, 35, 771–91.
  • Serrano-Aguilar PG, Lopez-Bastida J, Yanes-Lopes V. (2006). Impact on health-relateds quality of life and perceived burden of informal caregivers of individuals with Alzheimer’s diseae. Neuroepidemiology, 27, 136–42.
  • Silver EJ, Westbrook LE, Stein RE. (1998). Relationship of parental psychological distress to consequences of chronic health conditions in children. J Pediatr Psychol, 23, 5–15.
  • Sloper P, Turner S. (1993). Risk and resistance factors in the adaptation of parents of children with severe physical disability. J Child Psychol Psychiatry, 34, 167–88.
  • Thompson A, Fan MY, Unützer J, Katon W. (2008). One extra month of depression: The effects of caregiving on depression outcomes in the IMPACT trial. Int J Geriatr Psychiatry, 23, 511–16.
  • Wada K, Tanaka K, Theriault G, et al. (2007). Validity of the Center for Epidemiologic Studies Depression Scale as a screening instrument of major depressive disorder among Japanese workers. Am J Indus Med, 50, 8–12.
  • Wade SL, Taylor HG, Drotar D, et al. (1998). Family burden and adaptation during the initial year after traumatic brain injury in children. Pediatrics, 102, 110–16.
  • Yoo SH, Kim CS. (2004). An exploratory study on the effects of caregivers’ family relationship to the elderly with dementia: Focusing on problem, burdens and institutionalization. J Welfare Aged Inst, 26, 191–214.
  • Yoon HS, Ryu S. (2007). Factors associated with family caregivers’ burden of frail elders-comparing spouse with adults children. J Korea Gerontol Res, 27, 195–211.
  • Yun EG. (2010). A research on the how caregiving burden for the frail elder effect on caregiver’s guilt: Comparing between home-care elderly and nursing home. J Welfare Aged, 47, 289–308.
  • Zarit S, Reever K, Bach-Peterson J. (1980). Relatives of the impaired elderly: Correlates of feelings of burden. Gerontologist, 20, 649–55.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.