Skip Navigation
Skip to contents

J Korean Acad Nurs : Journal of Korean Academy of Nursing

OPEN ACCESS

Search

Page Path
HOME > Search
2 "Dependency burden"
Filter
Filter
Article category
Keywords
Publication year
Authors
Original Articles
Depression and Caregiving Burden in Families of Patients with Amyotrophic Lateral Sclerosis
Juyeon Oh, Ji Won An, Ki-Wook Oh, Seong-Il Oh, Jung A Kim, Seung Hyun Kim, Jeong Seop Lee
J Korean Acad Nurs 2015;45(2):202-210.   Published online April 30, 2015
DOI: https://doi.org/10.4040/jkan.2015.45.2.202
AbstractAbstract PDF
Purpose

The purpose of this study was to describe depression, caregiving burden and the correlation of the two variables in the families of patients with amyotrophic lateral sclerosis (ALS) and to clarify factors predicting caregiving burden.

Methods

A descriptive and cross-sectional study was conducted with 139 family members who provided care to patients with ALS. The characteristics of patients and families, Korean-Beck Depression Inventory (K-BDI), Korean version of Zarit Burden Interview (K-ZBI) and Korean-Amyotrophic Lateral Sclerosis Functional Rating Scale - Revised (K-ALSFRS-R) were used as study measures.

Results

The mean score for K-BDI was 19.39 out of 63 suggesting sub-clinical depression and 38.2% of the family members exhibited depression. The mean score for K-ZBI was 66.03 out of 88. The predictors for K-ZBI were K-BDI, age of family member, length of time spent per day in caring, relationship to patient and K-ALSFRS-R.

Conclusion

The results of this study suggest that levels of depression and caregiving burden are high among family members caring for patients with ALS. As depression is associated with caregiving burden, screening and emotional supports should be provided to reduce the burden of care for these family. Support programs to alleviate the care burden are also needed, considering family demographics, time per day in caring giving and K-ALSFRS-R.

Citations

Citations to this article as recorded by  
  • Effectiveness of the Mindfulness-Based Interventions for Caregivers of Patients with Amyotrophic Lateral Sclerosis: A Scoping Review
    Lutfiye İpek, Gokce Yagmur Gunes Gencer, Pınar Kısacık, Sibel Bozgeyik
    Journal of Nursology.2025; 28(1): 89.     CrossRef
  • Caring for people living with ALS in Korea: challenges and possible paths forward
    Crystal Jing Jing Yeo, Zachary Simmons
    Muscle & Nerve.2024; 70(5): 881.     CrossRef
  • The quality of life and depression in primary caregivers of patients with amyotrophic lateral sclerosis is affected by patient-related and culture-specific conditions
    Anna Maksymowicz-Śliwińska, Dorothée Lulé, Krzysztof NieporĘcki, Katarzyna Ciećwierska, Albert C. Ludolph, Magdalena Kuźma-Kozakiewicz
    Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration.2023; 24(3-4): 317.     CrossRef
  • The experiences of patients with amyotrophic lateral sclerosis of their decision‐making processes to invasive home mechanical ventilation—A qualitative study
    Tina Thorborg, Jeanette Finderup, Dorte Skriver Winther, Charlotte Kirkegaard Lorenzen, Pia Dreyer
    Nursing Open.2023; 10(8): 5139.     CrossRef
  • Psychological Support for Family Caregivers of Patients With Amyotrophic Lateral Sclerosis at the Time of the Coronavirus Disease 2019 Pandemic: A Pilot Study Using a Telemedicine Approach
    Minoo Sharbafshaaer, Daniela Buonanno, Carla Passaniti, Manuela De Stefano, Sabrina Esposito, Fabrizio Canale, Giulia D’Alvano, Marcello Silvestro, Antonio Russo, Gioacchino Tedeschi, Mattia Siciliano, Francesca Trojsi
    Frontiers in Psychiatry.2022;[Epub]     CrossRef
  • Factors associated with caring behaviors of family caregivers for patients receiving home mechanical ventilation with tracheostomy: A cross-sectional study
    Hyang Sook Kim, Chung Eun Lee, Yong Sook Yang, Tai-Heng Chen
    PLOS ONE.2021; 16(7): e0254987.     CrossRef
  • Family Caregiver Suffering in Caring for Patients with Amyotrophic Lateral Sclerosis in Korea
    Juyeon Oh, Jung-A Kim, Min Sun Chu
    International Journal of Environmental Research and Public Health.2021; 18(9): 4937.     CrossRef
  • Everyday life experiences of close relatives of people with amyotrophic lateral sclerosis receiving home mechanical ventilation—A qualitative study
    Dorte Winther, Charlotte Kirkegaard Lorenzen, Pia Dreyer
    Journal of Clinical Nursing.2020; 29(13-14): 2306.     CrossRef
  • Unmet supportive care needs mediate the relationship between functional status and quality of life in patients with amyotrophic lateral sclerosis
    Juyeon Oh, Seung Hyun Kim, Jung A Kim
    Palliative and Supportive Care.2019; 17(6): 650.     CrossRef
  • The Impact of Cognitive and Behavioral Symptoms on ALS Patients and Their Caregivers
    Jashelle Caga, Sharpley Hsieh, Patricia Lillo, Kaitlin Dudley, Eneida Mioshi
    Frontiers in Neurology.2019;[Epub]     CrossRef
  • Validity and Utility of the Center for Epidemiological Studies Depression Scale for Detecting Depression in Family Caregivers of Persons with Dementia
    Jiangbo Ying, Philip Yap, Mihir Gandhi, Tau Ming Liew
    Dementia and Geriatric Cognitive Disorders.2019; 47(4-6): 323.     CrossRef
  • Caregiving burden and depression in paid caregivers of hospitalized patients: a pilot study in China
    Yao-Dan Liang, Ya-Li Wang, Zhi Li, Li He, Ying Xu, Qing Zhang, Gui-Ying You, Xu-Hua Mi
    BMC Public Health.2018;[Epub]     CrossRef
  • The amyotrophic lateral sclerosis supportive care needs assessment instrument: Development and psychometric evaluation
    Juyeon Oh, Seong-il Oh, Jung A Kim
    Palliative and Supportive Care.2018; 16(6): 692.     CrossRef
  • Factors Influencing Psychosocial Well-Being in Family Caregivers of People with Amyotrophic Lateral Sclerosis
    Hyeon Sik Chu, Young Ran Tak, Seung Hyun Kim
    Journal of Korean Academy of Nursing.2018; 48(4): 454.     CrossRef
  • Factor analysis of the Zarit Burden Interview in family caregivers of patients with amyotrophic lateral sclerosis
    Juyeon Oh, Jung A. Kim
    Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration.2018; 19(1-2): 50.     CrossRef
  • An exploration into caring for a stroke-survivor in Lima, Peru: Emotional impact, stress factors, coping mechanisms and unmet needs of informal caregivers
    M. Amalia Pesantes, Lena R. Brandt, Alessandra Ipince, J. Jaime Miranda, Francisco Diez-Canseco
    eNeurologicalSci.2017; 6: 33.     CrossRef
  • Information-seeking Behavior and Information Needs in Patients With Amyotrophic Lateral Sclerosis
    Juyeon Oh, Jung A Kim
    CIN: Computers, Informatics, Nursing.2017; 35(7): 345.     CrossRef
  • Supportive care needs of patients with amyotrophic lateral sclerosis/motor neuron disease and their caregivers: A scoping review
    Juyeon Oh, Jung A Kim
    Journal of Clinical Nursing.2017; 26(23-24): 4129.     CrossRef
  • Convergence Study on Burden in Families Caregivers of Patients with Burn
    Gye-Hyun Jung, Hyun-Ju Na
    Journal of the Korea Convergence Society.2016; 7(6): 275.     CrossRef
  • 267 View
  • 6 Download
  • 19 Crossref
Close layer
Caregiver Burden in Caring for Elders Before and After Long-term Care Service in Korea
Hung Sa Lee
J Korean Acad Nurs 2012;42(2):236-247.   Published online April 30, 2012
DOI: https://doi.org/10.4040/jkan.2012.42.2.236
AbstractAbstract PDF
Purpose

Purposes of this study were: evaluation of family burden of caring for elders who receive long term care services, and examination of differences in burden before and after the introduction of long term care service in Korea.

Methods

Data were collected by questionnaires from 416 caregivers of elders who were registered with the Long Term Care Insurance Corporation in six cities. Data were collected in September, 2010 and analyzed using descriptive statistics, paired t-test, and ANOVA with the Scheffe test, and stepwise multiple regression.

Results

Family burden decreased significantly after long-term care service was initiated. Subjective burden decreased from 2.93 to 2.69 (t=11.78, p<.001), and objective burden, from 3.40 to 3.10 (t=12.73, p<.001). Stepwise multiple regression analysis revealed that factors affecting subjective burden were family relations (F=13.60, p=.003), age (F=5.47, p=.019), job (F=6.98, p=.008), and education (F=4.59, p=.032), and that factors affecting objective burden were living together (F=17.66, p<.001), job (F=13.34, p=.003), monthly income (F=6.61, p=.010), and type of service (F=6.62, p=.010).

Conclusion

The results of this first study to investigate caregiver burden after the Korean Long-term Care Insurance System was begun provide positive information for the development of strategies to decrease family burden in long term care.

Citations

Citations to this article as recorded by  
  • Comparison of Sleep Quality between Families of Dementia Patients and General Population in Community: Analysis with the Korea Community Health Survey
    Mina Kim, Young-Hoon Lee
    Korean Journal of Health Promotion.2023; 23(3): 139.     CrossRef
  • Registered Nurses’ Experiences of End-of-Life Care in Nursing Homes of South Korea: A Qualitative Study
    Soo-Jung Chang
    Healthcare.2022; 10(11): 2213.     CrossRef
  • Study on the Nutrient Intake and Dietary Quality of Elderly Residents on Various Meal Types in Long-Term Care Facility
    Hee-Sook Lim, Eun Bi Oh, Yoo Kyoung Park, Hae-Yun Chung
    Journal of the East Asian Society of Dietary Life.2020; 30(2): 172.     CrossRef
  • Factors Affecting Family Caregivers' Burden and Depression in Home-based Long-Term Care Service under the Long-Term Care Insurance System
    Hung Sa Lee, Chunmi Kim
    Journal of Korean Academy of Community Health Nursing.2018; 29(4): 530.     CrossRef
  • Effect of Family Caregiving on Depression in the First 3 Months After Spinal Cord Injury
    Min-Gu Kang, Chul-Hyun Kim, Eunhee Park, Jae-Won Huh, Won-Jong Yang, Tae-Woo Nam, Yu-Sun Min, Tae-Du Jung
    Annals of Rehabilitation Medicine.2018; 42(1): 130.     CrossRef
  • Relationship between caregiving burden and depression in caregivers of individuals with intellectual disabilities in Korea
    Su-Jung Nam, Eun-Young Park
    Journal of Mental Health.2017; 26(1): 50.     CrossRef
  • The Effect of Post-Stroke Depression on Rehabilitation Outcome and the Impact of Caregiver Type as a Factor of Post-Stroke Depression
    Dong-Heun Ahn, Yung-Jin Lee, Ji-Hun Jeong, Yong-Rok Kim, Jong-Bum Park
    Annals of Rehabilitation Medicine.2015; 39(1): 74.     CrossRef
  • Factors Related to Family Caregivers' Burden with the Community-Dwelling Disabled Elderly under the Long-Term Care Insurance System
    Eun-Jeong Han, Jung-Myun Lee, Jin-Hee Kwon, Seul-Bi Shin, Jung-Suk Lee
    Health Policy and Management.2014; 24(1): 71.     CrossRef
  • 294 View
  • 2 Download
  • 8 Crossref
Close layer

J Korean Acad Nurs : Journal of Korean Academy of Nursing
Close layer
TOP