Research in Community and Public Health Nursing

Original Articles

[English] Factors Associated with Work Engagement of Home-Visit Care Workers Based on Job Demands–Resources Model: A Quantitative Cross-Sectional Study: Hanyi Lee, Hyeon Sik Chu; Res Community Public Health Nurs. 2025;36(4):396-406. Published online December 31, 2025; DOI: https://doi.org/10.12799/rcphn.2025.01221

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Abstract PDF: Purpose
The aim of this study is to identify the factors associated with work engagement among home-visit care workers in South Korea, the Job Demands–Resources (JD-R) model was used as a guiding theoretical framework. Methods: This descriptive correlational study used secondary data from the 2020 Survey on the Service Environment of Home Care Workers by the Korea Institute for Health and Social Affairs. Participants were 509 certified home-visit care workers from Seoul and Chungcheong, each caring for one recipient. Measures included emotional labor, self-rated health, relationship quality with care recipients, and work engagement. Data were analyzed using hierarchical multiple regression. Results: Work engagement was negatively associated with emotional labor and positively associated with self-rated health, relationship quality with care recipient, and satisfaction with the care environment. Emotional labor remained a significant negative relationship, while self-rated health and relationship quality with care recipients emerged as key positive relationships. The final model explained 17.0% of the variance. Conclusions: These findings support the applicability of the JD-R model in understanding work engagement among home-visit care workers. Although job demands such as emotional labor may hinder engagement, individual and relational resources play protective and motivating roles. The diminished influence of physical and environmental factors in the presence of strong personal resources highlights the importance of a balanced approach that strengthens the emotional, physical, and relational capacities to support sustainable engagement.

[English] Factors associated with life satisfaction among family caregivers of persons living with dementia: Seonho Choi, Yeji Hwang, Eui Young Cho; Res Community Public Health Nurs. 2024;35(3):254-263. Published online September 30, 2024; DOI: https://doi.org/10.12799/rcphn.2024.00612

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Abstract PDF: Purpose
Because family caregivers provide a considerable amount of daily care to persons living with dementia, they are at risk of experiencing poor life satisfaction. Therefore, this study aimed to examine factors associated with the life satisfaction of family caregivers of persons living with dementia.
Methods
Data were collected through surveys from family caregivers (N=183), and a multiple linear regression analysis was conducted to examine the factors associated with their life satisfaction.
Results
The final model indicated that perceiving support from intimate others as helpful (β=.22, p<.001) was associated with greater life satisfaction, whereas a negative relationship with the care recipients (β=−.15, p=.046) and greater psychological burden (β=−.40, p<.001) were associated with poorer life satisfaction (Adjusted R2=0.49, F=20.42, p<.001).
Conclusion
Public policy should focus on providing greater support to family caregivers. Furthermore, healthcare professionals should implement intervention programs for family caregivers that focus on lowering their psychological burden.

[English] Priorities of Family Caregivers in Preserving Functional Abilities of Individuals with Alzheimer's Disease Living at Home: A Best-Worst Scaling Approach: Eunhye Cho, Youngran Yang, Hyun Kyung Kim, Hye Young Kim; Res Community Public Health Nurs. 2024;35(2):156-167. Published online June 28, 2024; DOI: https://doi.org/10.12799/rcphn.2024.00556

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Abstract PDF Supplementary Material: Purpose
The decline in cognitive abilities among individuals with Alzheimer’s disease significantly impacts their Activities of Daily Living (ADLs), creating challenges and stress for their caregivers. This study aimed to investigate the priorities of family caregivers of community-dwelling individuals with Alzheimer's disease concerning the preservation of their loved ones' ADLs.
Methods
We employed a cross-sectional design with a best-worst scaling approach (BWS), and developed a BWS questionnaire utilizing the 10 daily living items from the Disability Assessment for Alzheimer’s Disease scale. This questionnaire was administered to 132 caregivers of individuals with Alzheimer's disease. Data analysis was conducted using SPSS WIN 21.0 and the R statistical program.
Results
The results revealed that "using the toilet without accidents" emerged as the top-ranked ADL that family caregivers preferred to preserve for the longest duration among individuals with Alzheimer's disease living at home. In contrast, "Managing money appropriately" was identified as a daily living activity considered relatively less critical to preserve. The study further indicated a preference among caregivers for preserving physical ADLs over instrumental ADLs.
Conclusion
This research provides clinical evidence shedding light on the priorities of family caregivers in preserving the functional abilities of individuals with Alzheimer's disease within the community.

[Korean] The Relation among Uncertainty, Social Support, Care Burden of Mothers having Children with Developmental Disabilities: Kyoung Eun Jeong, Min Hyun Suk; Res Community Public Health Nurs. 2023;34(2):117-126. Published online June 30, 2023; DOI: https://doi.org/10.12799/rcphn.2022.00346

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Abstract PDF

Purpose
This descriptive correlation study aimed to confirm the relation among uncertainty, social support, care burden of mothers having children with developmental disabilities.
Methods
The participants were 111 mothers having children with autistic spectrum disorder or intellectual disability. The collected data were analyzed by descriptive statistics, t-test, ANOVA, Pearson’s correlation coefficient and multiple regression using IBM SPSS 23.0 in the study.
Results
Uncertainty and social support were significantly correlated to caregiver burden. As a result of multiple regression analysis, the factors affecting caregiver burden were children’s age, the expense for caring, the period suspected child disabilities, and uncertainty. These factors accounted for 40.8% of caregiver burden.
Conclusion
In order to reduce the burden of caring for mothers with children with developmental disabilities, it is necessary to establish a system that can detect children with developmental disabilities early and to develop and provide an integrated guide suitable for the growth and development stage of children with developmental disabilities.

Citations

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Factors associated with uncertainty in parents of children with developmental disabilities: A scoping review
Heejung Choi, GyeongAe Seomun, Jeongeun Song
Disability and Health Journal.2026; 19(1): 101962. CrossRef
The effect of intolerance of uncertainty, sleep quality, and social support on caregiver burden in parents of children with chronic diseases: A cross-sectional study
Furkan Doğaner, Raziye Celen
Journal of Pediatric Nursing.2025; 81: e106. CrossRef
Adaptation and validation of the Korean version of the parental perception of uncertainty scale (K-PPUS) in parents of children with developmental disabilities
Heejung Choi, GyeongAe Seomun
Journal of Pediatric Nursing.2025; 82: 47. CrossRef
The effect of counseling services provided in rehabilitation centers on parents' caregiving burden and quality of life
Mehmet Uçar, Rukuye Aylaz
WORK: A Journal of Prevention, Assessment & Rehabilitation.2025; 81(2): 2763. CrossRef
Spousal support, parent–nurse partnership and caregiver burden among parents of children with chronic diseases: A cross‐sectional study
Jihye Kim, Heemin Chae, Yoonjung Kim
Journal of Clinical Nursing.2024; 33(7): 2649. CrossRef

[English] The Burden Experience of Family Caregiver of Older Adults with Chronic Illness: Nova Yustisia, Titin Aprilatutini, Tuti Anggriani Utama, Mahmasoni Masdar; Res Community Public Health Nurs. 2023;34(2):85-95. Published online June 30, 2023; DOI: https://doi.org/10.12799/rcphn.2022.00304

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Abstract PDF

Purpose
This study aims to find out further about the burden on families in undertaking caregiving for the elderly with chronic illnesses.
Methods
A qualitative study was developed using in-depth interviews with 12 family caregivers selected by purposive sampling in July 2022. The thematic analysis was then carried out using the Colaizzi method, and N-Vivo 12 Qualitative Data Analysis Software was used to assist with the content analysis.
Results
The result from the experience interview analysis of caregivers participating in this study were 54 codes which were categorized into thirteen categories. Then, they were derived into four themes, as follows: 1) Physical burden of the caregivers for the elderly with chronic illness, 2) Psychological burden of the caregivers for the elderly with chronic illness, 3) Obstacle of caregivers for the elderly with chronic illness, 4) The state of caregivers who perform caregiving for the elderly with chronic illness.
Conclusion
The experience of caregivers in undertaking caregiving for the elderly with chronic disease has many obstacles, such as physical, psychological, and economic burdens. Caregivers often find positive aspects of their experiences while caregiving for the elderly, although their burden also constantly increases. Health facilities should pay serious attention to family caregivers and facilitate programs that can help reduce the burden on family caregivers.

Citations

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Mastering the Art of Caregiving: Instructional Approaches to Teaching Healthcare‐Related Procedural Skills to Informal Caregivers—An Integrative Review
An Ling Siew, Esther Yin Hui Chew, Ee‐Yuee Chan, Elaine Kee Chen Siow
Journal of Advanced Nursing.2026; 82(1): 272. CrossRef
Enhancing Communication and Empathy Skills in Geriatric Care: Nurses' Reflections on Simulation‐Based Training for Patient Interaction and Education
Sobhia Ahmed Abdel Kader Mohammed, Mostafa Shaban
Journal of Clinical Nursing.2025;[Epub] CrossRef
Spirituality Well-Being, Health Status, Nutritional Status and Their Relation to Illness Perception in Chronic Obstructive Pulmonary Disease
Scholastica Fina Aryu Puspasari, Margaretha Kurniastuti, Kosen d'Aristo McGenggeng
Jurnal Berita Ilmu Keperawatan.2025; 18(2): 193. CrossRef
Relationship between Care Burden and Health Anxiety in the Family Caregivers of the Older Adults with Alzheimer’s Disease
Mohammad Sadegh Sargolzaei, Daniyal Kohestani, Tahereh Alsadat Khoubbin Khoshnazar, Hossein Asghari Asl
Ageing International.2024; 49(2): 280. CrossRef

[English] Perceived Social Support of Family Caregivers for People with Dementia: Concept Analysis: Aeri Kim, Jeong Yeon Kim, Kyung Mi Woo; J Korean Acad Community Health Nurs. 2021;32(4):540-554. Published online December 31, 2021; DOI: https://doi.org/10.12799/jkachn.2021.32.4.540

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Abstract PDF

Purpose
Most of the currently used concepts and measurements of social support have been relevant for general population. The main purpose of this study is to conduct the concept analysis of perceived social support(PSS) of family caregivers for people with dementia. Methods: This study adopted the Walker and Avant concept analysis methodology. Results: Findings from this concept analysis suggested four defining attributes of PSS of family caregivers for people with dementia: 1) PSS is help or assistance that family caregivers perceive as available when needed; 2) PSS is offered through socio-ecological structure; 3) PSS has a specific function to meet the needs of family caregivers; and 4) PSS includes quality aspects where family caregivers choose, use, or evaluate it. Borrowing from the socio-ecological model, this study proposed the structural aspects of PSS. This study also identified functional aspects of PSS, such as emotional support, informational support, appraisal support, and practical support. Finally, this study assessed quality aspects of PSS, such as satisfaction, timeliness, usefulness, accessibility, and coordination. Conclusion: Focusing on family caregivers for people with dementia, we proposed a new model of PSS. The present study helped refine and clarify the concept of PSS of family caregivers for people with dementia. The results of this study may also contribute to promoting the development of more effective instruments for the concept.

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Examining Characteristics and Service Utilization of South Korean Home Health Care Patients: Secondary Analysis of 10-Year Data From a Tertiary Hospital
Hana Lee, Aeri Kim, Hyunsook Heo, Jisoo Lee, Kyungmi Woo
Home Health Care Management & Practice.2023; 35(1): 21. CrossRef
Experience of family caregivers using dementia management programs for patients with dementia during COVID-19: Based on focus group interviews
Doonam Oh, Jeonghae Hwang, Seonghee Jeong
Korean Journal of Health Education and Promotion.2022; 39(5): 101. CrossRef

[English] Influencing Factors Affecting Caregivers’ Service Quality for the Elderly with Dementia: Focusing on Dementia Knowledge, Work Value, and Job Performance Confidence: Doo Ree Kim, Kwang Hwan Kim, Soo Yeon Lee, Sun Hee Han, Gi Ran Lee; J Korean Acad Community Health Nurs. 2021;32(3):233-242. Published online September 30, 2021; DOI: https://doi.org/10.12799/jkachn.2021.32.3.233

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Abstract PDF

Purpose
The purpose of this study was to verify influencing factors affecting service quality provided by caregivers working for the elderly with dementia.
Methods
Data were collected using a self-reported questionnaire from 214 caregivers in a long-term care facility in D city. The data were analyzed with service quality, dementia knowledge, work value, and job performance confidence. For data analysis, the descriptive statistics, t-test, one-way ANOVA, Pearson correlation coefficients, and multiple regression were performed using SPSS/WIN 21.0 program.
Results
There were significant differences in service quality depending on the health status. Factors influencing service quality were work value, and job performance confidence with R² value of 38%. The highly influencing factors were work value, and job performance confidence.
Conclusion
The results of this study indicate that the effort to improve the service quality of caregivers should focus on work value and job performance confidence.

Citations

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The subjectivity of care workers’ perception on remaining functional ability care: A Q methodology approach
Hyunjung Doo, Soonmi Park
Journal of Korean Gerontological Nursing.2023; 25(1): 56. CrossRef

[English] A Delphi Study for Developing a Person-centered Dementia Care Online Education Program in Long-term Care Facilities: Da Eun Kim, Hae Sagong, Ju Young Yoon; J Korean Acad Community Health Nurs. 2019;30(3):295-306. Published online September 30, 2019; DOI: https://doi.org/10.12799/jkachn.2019.30.3.295

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Abstract PDF

PURPOSE
There has been a growing recognition that person-centered care enhances the quality of life of nursing home residents with dementia. This study was conducted to develop a person-centered dementia care online education program for direct care staff in long-term care facilities.
METHODS
Delphi method with expert group was used to validate contents. We developed 61 draft items based on literature review. Twenty experts participated in consecutive three round surveys including 5-point Likert scale questions and open-ended questions. Based on experts' opinions, the content validity ratio for content validity and the coefficient of variation for stability were calculated.
RESULTS
Three-round Delphi surveys and additional feedback from the expert panel established a consensus of core contents: 1) dementia (7 categories), 2) person-centered care (6 categories), 3) communication (8 categories), and 4) behavioral and psychological symptoms of dementia (6 categories). Specific sub-categories in each category were differentiated according to the job qualifications (65 sub-categories for registered nurses, 64 sub-categories for nursing aids, and 41 sub-categories for personal care workers).
CONCLUSION
This delphi study identified person-centered dementia education curricula, in which the person-centered approach should be a key policy priority in Korean long-term care system. Now it is urgently needed to develop education programs utilizing online platforms that enable efficient and continuous learning for long-term care staff, which can contribute to behavior changes in the person-centered dementia care approach and improvement of care quality in long-term care facilities.

Citations

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Moral sensitivity and person‐centred care among mental health nurses in South Korea: A cross‐sectional study
Sun Joo Jang, Eun Hye Kim, Haeyoung Lee
Journal of Nursing Management.2022; 30(7): 2227. CrossRef
Personhood Communication with Persons with Dementia: Concept Analysis
Jiyeon Kim, Jun-Ah Song
Journal of Korean Gerontological Nursing.2021; 23(4): 406. CrossRef
Validity and Reliability of the Korean Version of Person-Centered Practice Inventory-Staff for Nurses
Sohyun Kim, Sunghee H Tak
Journal of Korean Academy of Nursing.2021; 51(3): 363. CrossRef
Development and Evaluation of a Person-centered Dementia Care Education Program for Nursing Home Staff
Eun-Hi Kong
Journal of Korean Gerontological Nursing.2020; 22(3): 247. CrossRef

[English] Factors Affecting Family Caregivers' Burden and Depression in Home-based Long-Term Care Service under the Long-Term Care Insurance System: Hung Sa Lee, Chun Mi Kim; J Korean Acad Community Health Nurs. 2018;29(4):530-538. Published online December 31, 2018; DOI: https://doi.org/10.12799/jkachn.2018.29.4.530

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Abstract PDF

PURPOSE
This study tried to identify changes in family burden after the introduction of the long-term care insurance and to examine the factors influencing subjective and objective caring burden and depression of family caregivers of elders receiving home-based long-term care.
METHODS
Data were collected from 203 family caregivers of elders from August 1 to 31, 2015 using questionnaires. They were analyzed in descriptive statistics, t test, ANOVA test, and multiple regression analysis.
RESULTS
The mean score of depression was 7.24, which suggested mild depression level. The subjective family burden was 2.71 and the objective burden 3.04. The factors affecting depression included subjective burden (t=5.08, p < .001), objective burden (t=2.80, p=.006), time of elderly care per day (t=âˆ’3.61, p < .001), caregiving duration (t=3.33, p=.001), age (t=3.13, p=.002), family relationship (t=2.48, p=.014), and economic status (t=1.99, p=.047).
CONCLUSION
The family burden was most important influencing factor on caregiver's depression. Therefore, services and supports to alleviate caregivers' burden in the home-based care should be added to long-term care.

Citations

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The moderating effect of care time on care-related characteristics and caregiver burden: differences between formal and informal caregivers of dependent older adults
Eunmi Oh, SeolHwa Moon, Daum Chung, Rina Choi, Gwi-Ryung Son Hong
Frontiers in Public Health.2024;[Epub] CrossRef
The effect of self-rated health on depressive symptoms in Chinese older adults: The mediating role of social participation and spouse health
Chi Zhang, Yinan Zhao, Xiaoyang Li, Yongzhen Guo, Ruotong Peng, Xiao Wan, Qin Zhou, Juan Yang, Siliang Wu, Hui Feng
Geriatric Nursing.2024; 59: 411. CrossRef
Working Conditions Affecting Home Care Workers’ Stress and Turnover Intention
Samsik Lee, Gyeongrim Oh
Journal of Applied Gerontology.2023; 42(4): 717. CrossRef
Relationship between filial obligation and caregiver depression among adult children: A systematic review and meta‐analysis
Yuqin Pan, Ruyi Chen, Dongliang Yang
Nursing Open.2023; 10(6): 3474. CrossRef

[English] Experience of a Special Rating Dementia Service for Family Caregivers of Elderly People with Dementia: Hee Kyung Cho, Soo Jung Chang; J Korean Acad Community Health Nurs. 2018;29(2):231-243. Published online June 30, 2018; DOI: https://doi.org/10.12799/jkachn.2018.29.2.231

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Abstract PDF: PURPOSE
This study tries to explore experiences with a special rating dementia service among family caregivers of elderly people with dementia.
METHODS
The participants were 11 family caregivers of elderly people with dementia and had used a day-care service from the special rating dementia service for more than 3 months. Data were collected through individual in-depth interviews and analyzed using content analysis.
RESULTS
Three categories emerged: â€œreminiscence of an entangled lifeâ€, â€œfeeling relieved from a stifled lifeâ€, and â€œhope for a better life through help and supportâ€ with 8 sub-categories and 23 codes. By using the special rating dementia service, the participants experienced relief from the burden of caring for their elderly family member with dementia and restored their social relations or family relationships. They experienced a positive transition in which their caring for elderly family members with dementia was integrated into their daily lives, and they expressed their desires for better policies.
CONCLUSION
These findings imply the importance and necessity of the special rating dementia service. Practical and systematic family support programs are necessary and proactive publicity activities by the government and public agencies are suggested to ensure that family caregivers can easily use the special rating dementia system.

[English] Factors Influencing Burnout in Primary Family Caregivers of Hospital-based Home Care Patients: Ju Ok Yang, Hye Kyung Lee; J Korean Acad Community Health Nurs. 2018;29(1):54-64. Published online March 31, 2018; DOI: https://doi.org/10.12799/jkachn.2018.29.1.54

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3 Citations

Abstract PDF

PURPOSE
The purpose of this study is to identify factors influencing burnout in primary family caregivers of Home Health Care Patients.
METHODS
Data were collected from 121 primary family caregivers of home health care patients in three different hospitals in â€˜Dâ€™ metropolitan city and the study was conducted from August 10, 2016 to January 17, 2017. The data were analyzed using descriptive statistics, t-test, ANOVA, Pearson's Correlation Coefficient, Stepwise Multiple Linear Regression.
RESULTS
Mean scores for the nursing needs of the participants were 3.54Â±0.79, the family functions were 1.24Â±0.58, the burnouts were 2.74Â±0.49. The burnouts were positively correlated with the nursing needs but inversely correlated with the family function. The factor that had the greatest influence on the burnouts of primary family caregivers of Home Health Care was family function (Î²=âˆ’.245, p=.001), followed by patients' daily activity (Î²=âˆ’.213, p=.014), age (Î²=.208, p=.032), monthly nursing services cost (Î²=âˆ’.196, p=.044) and nursing needs (Î²=.129, p=.014). The Explanatory Power of Models was 23%.
CONCLUSION
Individually customized home care nursing intervention programs are required to be provided in accordance with patient's family function and daily activity, monthly home care nursing service cost, nursing needs and general characteristics of primary caregivers of Home Health Care Patients such as their age, the number of family members living together, sex and the name of disease.

Citations

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Roles and Problems of Stroke Caregivers: A Qualitative Study in Yogyakarta, Indonesia
Paryono Muhrodji, Hendrawan Dian Agung Wicaksono, Sekar Satiti, Laksono Trisnantoro, Ismail Setyopranoto, Amelia Nur Vidyanti
F1000Research.2022; 10: 380. CrossRef
Roles and Problems of Stroke Caregivers: A Qualitative Study in Yogyakarta, Indonesia
Paryono Muhrodji, Hendrawan Dian Agung Wicaksono, Sekar Satiti, Laksono Trisnantoro, Ismail Setyopranoto, Amelia Nur Vidyanti
F1000Research.2021; 10: 380. CrossRef
Influence of Self-care on Burnout in Primary Family Caregiver of Person with Dementia
Jeong Hwa Kwon, Gwi-Ryung Son Hong
Journal of Korean Academy of Nursing.2021; 51(2): 217. CrossRef

[English] An Intervention Study of Self-feeding for the Elderly in Nursing Homes: Kyung Hee Lee; J Korean Acad Community Health Nurs. 2017;28(4):450-462. Published online December 31, 2017; DOI: https://doi.org/10.12799/jkachn.2017.28.4.450

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Abstract PDF

PURPOSE
This study aims to investigate the effects of an intervention of self-feeding for elderly residents who were eating with assistance or eating by himself/herself with spilling food.
METHODS
The Participants were 11 elderly people and 6 formal caregivers from 7 nursing homes in Korea. The intervention was to use the spoon and chopstick sets designed for compensating the weakened eating function. Both quantitative and qualitative data were collected through observation, structured questions, and in-depth interviews.
RESULTS
The mealtime was significantly increased by 3.2 minutes (p=.011) after the intervention. Three themes were extracted for the meaning of self-feeding expressed by the elders; fighting alone for self-feeding, pride of participating in the study, and burden for self-feeding and research participation. Caregivers expressed the meaning of the elder's self-feeding such as the regret of missed chances, facilitating rehabilitation, the increase of the eating pleasure and quality of care, and ambivalence.
CONCLUSION
Self-feeding has become an opportunity to recognize life values for the elders in nursing homes; for the caregivers, to reconsider caring of the elderly. Posture and eating utensils were also important to improve self-feeding skills.

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Structure Healthcare Standards and Criteria That Contribute to the Care of Residents in Homes for the Elderly: A Narrative Review
Victor Mathias, Ethelwynn L. Stellenberg, Mariana van der Heever
Journal of Aging and Environment.2024; 38(4): 367. CrossRef

[English] Factors Influencing Quality of Caregiving by Caregivers for Elders with Dementia: Chan Mi Kang, Jung Soon Kim, Jeong Hee Jeong; J Korean Acad Community Health Nurs. 2016;27(3):193-201. Published online September 30, 2016; DOI: https://doi.org/10.12799/jkachn.2016.27.3.193

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6 Citations

Abstract PDF

PURPOSE
The aim of the study is to determine factors influencing quality of caregiving by caregivers for the elderly with dementia.
METHODS
Data were collected from 87 caregivers for elders with dementia who had visited in Busan Metropolitan Center for Dementia and D-University hospital outpatient center from July 10 to September 30, 2015. A self-reported questionnaire was used to assess the severity of the elders' dementia and knowledge of dementia, burdens and quality of caregiving by the caregivers. The SPSS 21.0 version program was used for data analysis. Data were analyzed using descriptive statistics, Pearson's correlation, t-test, ANOVA and multiple regression.
RESULTS
Significant predictors of quality of caregiving by caregivers included caregivers' burdens (explanation power 25%), knowledge of dementia (explanation power 4%) and levels of education (explanation power 3%). These factors explained 32.3% of the variances in quality of caregiving.
CONCLUSION
Burdens on caregivers were a major factor that decreased quality of caregiving, and knowledge of dementia was a factor that increased it. These findings show that educational programs and intervention for reducing burdens and improving knowledge of dementia are necessary to improve quality of caregiving by caregivers.

Citations

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Factors influencing the care burden among family caregivers using dementia care centers for older adults with dementia in Korea: a cross-sectional descriptive study
Ja Eun Kim, Soo Jin Lee
Journal of Korean Biological Nursing Science.2024; 26(4): 382. CrossRef
Depression, Anxiety and Associated Factors in Family Caregivers of People With Dementia
Su-Jeong Hong, Eyohan Ko, Malrye Choi, Nam-Ju Sung, Myeong-Il Han
Journal of Korean Neuropsychiatric Association.2022; 61(3): 162. CrossRef
Informal Caregiving and Alzheimer’s Disease: The Psychological Effect
Emily Hellis, Elizabeta B. Mukaetova-Ladinska
Medicina.2022; 59(1): 48. CrossRef
Influence of Self-care on Burnout in Primary Family Caregiver of Person with Dementia
Jeong Hwa Kwon, Gwi-Ryung Son Hong
Journal of Korean Academy of Nursing.2021; 51(2): 217. CrossRef
Relationship between Caring Burden and Caring Behavior among Family Caregivers of Elderly with Dementia in Community-Dwelling: Mediating Effects of Caring Self-Efficacy and Social Support
Young Ju Oh, Myung Ha Lee, Hee Sun Kim
Korean Journal of Adult Nursing.2020; 32(2): 186. CrossRef
Factors Affecting the Care Burden of Nurses Caring Elderly Patients with Dementia
Doo Ree Kim, Eun-Kyoung Han
Journal of Korean Academy of Community Health Nursing.2019; 30(3): 368. CrossRef

[English] Exploring Psycho-social Determinants to Child Neglect and Abuse among Caregivers with Young Children: Ah Rim Kim, Young Ran Tak; J Korean Acad Community Health Nurs. 2016;27(1):81-94. Published online March 31, 2016; DOI: https://doi.org/10.12799/jkachn.2016.27.1.81

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PURPOSE
The objective of this study was to investigate the relations among psycho-social factors regarding child neglect and abuse using the data from the 2013 Korea National Survey on Children and Youth.
METHODS
Data from a sample of 1,062 primary caregivers with young children were analyzed with the SPSS and AMOS programs to examine the interrelationships among depression, parenting stress, marital satisfaction, parent-child attachment, and child neglect or maltreatment.
RESULTS
Depression, stress, and attachment had a direct influence on child neglect and abuse. Satisfaction with marital relationship, parenting stress, and attachment were found to play mediating roles in accounting for child neglect and abuse, explaining 12% of the variance. The results of multi group path analysis showed that some coefficients were different according to the age group of the children. For caregivers with infants, parenting stress did not predict either attachment or child maltreatment, whereas for caregivers with toddlers, depression did not have a significant effect on attachment.
CONCLUSION
In order to prevent child maltreatment, efforts should be made to develop community-based psycho-social support interventions focused on marital relationship as well as parent-child dyads and to provide practical child care support.

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Risk factors for child maltreatment in South Korea: An investigation of a nationally representative sample
Jaejin Ahn, Joan P. Yoo
Asian Social Work and Policy Review.2019; 13(3): 282. CrossRef
Validation of the Korean Version of the Maternal Postpartum Attachment Development Scale for Mothers of Children who were in a Neonatal Intensive Care Unit
Ah Rim Kim, Young Ran Tak
Korean Journal of Child Studies.2018; 39(1): 129. CrossRef

[English] The Effectiveness of Dementia Education for the Nursing Method of Family Caregivers of the Demented Elderly: Kwang Soo Yoo, Eun Sun So; J Korean Acad Community Health Nurs. 2014;25(2):97-108. Published online June 30, 2014; DOI: https://doi.org/10.12799/jkachn.2014.25.2.97

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Abstract PDF

PURPOSE
This study attempted to identify the effectiveness and substantiality of a dementia education program for family caregivers of the demented elderly.
METHODS
This quasi-experimental study using a nonequivalent control pretest-posttest design was carried out from April 15 to July 29 in 2012 with 137 subjects divided into an experimental group (n=70) and a control group (n=67). This study examined the subjects' general characteristics, and evaluated their nursing method four times, respectively, before the intervention, right after the intervention, and 2 and 4 weeks after the intervention, and then analyzed collected data through t-test and chi2-test.
RESULTS
In the experimental group that had received the dementia education, the nursing method score was significantly higher right after the intervention (t=8.33, p<.001) and 2 weeks after the intervention (t=8.01, p<.001) than before the intervention, but their score 4 weeks after the intervention was not significantly different from that of the control group (t=1.08, p=.28).
CONCLUSION
The dementia education was found to be effective in improving the nursing method of family caregivers of the demented elderly. This study implies that further follow-up dementia education is necessary between 2 and 4 weeks to maintain the effectiveness.

Citations

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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
The effect of a comprehensive mobile application program (CMAP) for family caregivers of home‐dwelling patients with dementia: A preliminary research
Eunsil Park, Heeok Park, Eun Kyung Kim
Japan Journal of Nursing Science.2020;[Epub] CrossRef
Comparing the Needs of Family Caregivers and Program Providers in Long-Term Care in Terms of Family Support Program
Myonghwa Park, Younghye Go, Miri Jeong, Eun-Jeong Han
Korean Journal of Adult Nursing.2019; 31(1): 14. CrossRef
The Effects of a Support Program for Family Caregivers of Elderly with Dementia on Empowerment and Attitudes toward Dementia
So Yoon Kim, Seonghee Jeong
Journal of Korean Academic Society of Nursing Education.2019; 25(1): 103. CrossRef
Factors associated with Burden of Family Caregivers of Home-dwelling Elderly People with Dementia: A Systematic Review and Meta-analysis
Eun Kyung Kim, Heeok Park
Korean Journal of Adult Nursing.2019; 31(4): 351. CrossRef

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