The effect of caregiver support on mental health outcomes in women caring for family members living with chronic illnesses: A case of Motsinoni village in Mopani district

Phoke Alpha Rakgwata; Tsireledzo Sikhitha; Decent Munzhelele

doi:10.20525/ijrbs.v14i6.4114

Authors

Phoke Alpha Rakgwata Department of Social Work, University of Venda https://orcid.org/0009-0003-0395-8951
Tsireledzo Sikhitha Department of Social Work, University of Venda, Faculty of Humanities, Social Sciences and Education, Thohoyandou, University Road X5050, South Africa. https://orcid.org/0000-0002-8913-5643
Decent Munzhelele Department of Social Work, University of Venda, Faculty of Humanities, Social Sciences and Education, Thohoyandou, University Road X5050, South Africa https://orcid.org/0009-0004-7779-9954

DOI:

https://doi.org/10.20525/ijrbs.v14i6.4114

Keywords:

Caregiver Support, Mental Health, Chronic Illness, Women, Motsinoni Village, Qualitative Research, Community Resources.

Abstract

This article looks at how carer support affects the mental health outcomes of women who look after family members with chronic illnesses in Motsinoni Village, Mopani District, South Africa. Caring for someone with a chronic illness is a difficult responsibility that frequently results in significant physical, mental, and emotional pain for those who provide it. Given the predominantly female caregiving population in this area, understanding their unique mental health challenges is vital. The research employed qualitative research approach with an in-depth interview 6 participants out of 30 women using 20% population sampling norm, exploring their experiences and perceptions regarding caregiver support systems. The findings reveal that emotional, social, and informational support significantly enhance the mental well-being of these women, easing feelings of isolation and stress associated with caregiving. Participants reported that access to community resources and support groups led to improved coping strategies, resilience, and overall mental health. However, a lack of institutional support often resulted in increased anxiety and depressive symptoms. This study highlights the importance of establishing comprehensive support networks to strengthen the mental health of female caregivers, thereby improving their quality of life. In conclusion, empowering caregivers through targeted interventions can mitigate mental health issues and foster a sustainable caregiving environment.

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References

American Psychological Association. (2022). Caregiver stress: The importance of mental health care for caregivers. American Psychological Association.

Amin, T. (2021). The psychosocial impact of caregiving on women in rural settings: A case study from rural India. Journal of Rural Health, 42(3), 321–331.

Bernstein, L., & Gallo, W. T. (2019). Caring for older adults presents a set of psychological, emotional, and logistics issues that differ from childcare. In Barriers, challenges, and supports for family caregivers in science, engineering, and medicine: Proceedings of two symposia. National Academies Press.

Bowen, M. (1978). Family therapy in clinical practice. Jason Aronson.

Broderick, C. B., & Smith, A. L. (2002). The family: A sociological interpretation. Prentice Hall.

Cagle, J. G., & Smith, D. L. (2021). Structural barriers to caregiving: A comprehensive review of caregiving support systems. Journal of Applied Gerontology, 40(9), 1027–1044. https://doi.org/10.1177/0733464820900700

Cheung, A. (2023). Language teaching during a pandemic: A case study of Zoom use by a secondary ESL teacher in Hong Kong. RELC Journal, 54(1), 55–70. https://doi.org/10.1177/0033688220981784 DOI: https://doi.org/10.1177/0033688220981784

Chiao, C. Y., Wu, H. S., & Hsiao, C. Y. (2016). Caregiver burden in caregivers of patients with dementia: A longitudinal study. Journal of Aging & Health, 28(4), 564–582.

Choi, H., & Lee, H. (2019). The effects of caregiver support on mental health outcomes in chronic illness caregiving. Journal of Family Psychology, 33(4), 429–438. https://doi.org/10.1037/fam0000571 DOI: https://doi.org/10.1037/fam0000571

Cohen, M. A., & Haldane, A. (2020). Emotional resilience in caregiving: Coping mechanisms and social support. Social Work in Health Care, 59(10), 813–826. https://doi.org/10.1080/00981389.2020.1842268

Creswell, J. W., & Poth, C. N. (2018). Qualitative inquiry and research design: Choosing among five approaches (4th ed.). Sage Publications.

Cruz, E., Par'e, M. A., Stan, C., Voth, J., Ward, L., & Taboun, M. (2024). Caring for the caregiver: An exploration of the experiences of caregivers of adults with mental illness. Qualitative Research in Health, 5, 100406. https://doi.org/10.1016/j.ssmqr.2024.100406 DOI: https://doi.org/10.1016/j.ssmqr.2024.100406

Green, J., & Thorogood, N. (2018). Qualitative methods for health research (4th ed.). Sage Publications.

Grice, A., & Walker, R. (2012). Mental health outcomes of family caregivers in chronic illness contexts. Journal of Health and Social Behavior, 53(1), 11–25. https://doi.org/10.1177/0022146511429063

Hinojosa, M. S., Griffiths, S., & Hernaez, R. (2017). The importance of social support in caregiving: A case study of elderly caregivers in Mexico. Journal of Family Studies, 43(1), 57–68.

Kaye, L. K., & Barlow, A. (2021). Advocating for policies and programs that recognize the importance of mental health care in the lives of caregivers is essential. American Psychological Association.

Khoa, B. T., Hung, B. P., & Hejsalem-Brahmi, M. (2023). Qualitative research in social sciences: Data collection, data analysis, and report writing. International Journal of Public Sector Performance Management, 12(1–2), 187–209. https://doi.org/10.1504/IJPSPM.2023.132247 DOI: https://doi.org/10.1504/IJPSPM.2023.132247

Lee, M., & Lee, J. H. (2020). Access to caregiver resources: A systematic review of barriers and facilitators. Journal of Aging & Social Policy, 32(1), 37–56. https://doi.org/10.1080/08959420.2020.1748382

Machemedze, R., & Murwira, J. (2020). Barriers to healthcare access in rural communities of southern Africa: A review of challenges and proposed solutions. African Health Journal, 9(2), 112–120.

Marziale, M. H., & Souza, D. (2021). Traditional caregiving practices: Insights from different cultures. Journal of Transcultural Nursing, 32(5), 451–459. https://doi.org/10.1177/1043659621991369

Maxwell, J. A. (2021). Why qualitative methods are necessary for over-generalisation. Qualitative Psychology, 8(1), 111–118. https://psycnet.apa.org/doi/10.1037/qup0000173 DOI: https://doi.org/10.1037/qup0000173

McNamara, M., & Gibbons, D. (2021). Caregiver stress and barriers to healthcare: Insights from caregiver interviews. Journal of Family Social Work, 24(2), 132–150. https://doi.org/10.1080/10522158.2021.1862087

Murphy, J. M., & O’Donovan, C. (2014). Family caregiving and mental health: A review of the evidence. Journal of Family Psychology, 28(1), 56–67. https://doi.org/10.1037/fam0000164 DOI: https://doi.org/10.1037/fam0000164

Neff, J., & Spector, A. (2021). Coping strategies for caregivers in chronic illness care: From informal to formal care options. Health Psychology, 40(7), 496–507. https://doi.org/10.1037/hea0001050 DOI: https://doi.org/10.1037/hea0001050

Nguyen, T. T., & Nguyen, S. D. (2020). Cultural factors in caregiving practices: A study of immigrant families in the U.S. Journal of Cross-Cultural Psychology, 51(6), 489–505. https://doi.org/10.1177/0022022119876851

Nikolopoulou, K. (2023). Inclusion and exclusion criteria: Examples & definition. Scribbr. https://www.scribbr.com/methodology/inclusion-exclusion-criteria

Pearlin, L. I., & Skaff, M. M. (2021). Caregiving and mental health: Challenges and pathways for intervention. American Journal of Geriatric Psychiatry, 29(7), 687–696. https://doi.org/10.1016/j.jagp.2021.03.006 DOI: https://doi.org/10.1016/j.jagp.2021.03.006

Phillips, R., Durkin, M., Engward, H., & Iancu, M. (2022). The impact of caring for family members with mental illnesses on the caregiver: A scoping review. Health Promotion International, 38, 1–23. https://doi.org/10.1093/heapro/daac049 DOI: https://doi.org/10.1093/heapro/daac049

Pinquart, M., & Sörensen, S. (2016). Gender differences in caregiver stress: A meta-analysis. Psychology of Aging, 31(3), 422–431.

Pugliesi, K., & Shook, K. (2016). Social support, caregiving, and well-being in the context of chronic illness. Social Science & Medicine, 150, 1–9. https://doi.org/10.1016/j.socscimed.2015.12.021 DOI: https://doi.org/10.1016/j.socscimed.2015.12.021

Saldaña, J. (2016). The coding manual for qualitative researchers (3rd ed.). Sage Publications.

Schulz, R., & Sherwood, P. R. (2017). Physical and mental health effects of family caregiving. Journal of Social and Clinical Psychology, 36(9), 745–755.

Skinner, J., Edwards, A., & Smith, A. C. (2020). Qualitative research in sport management. Routledge. https://doi.org/10.4324/9780367854249 DOI: https://doi.org/10.4324/9780367854249

Smith, D. L., Jones, R., & Weaver, M. (2020). Social and economic impacts of caregiving in rural communities. Rural Health Perspectives, 29(1), 78–90.

Walsh, F. (2003). Normal family processes: Growing diversity and complexity (3rd ed.). Guilford Press. DOI: https://doi.org/10.4324/9780203428436

Zarit, S. H., Reever, K. E., & Bach-Peterson, J. (2019). Relatives of the impaired elderly: Correlates of feelings of burden. The Gerontologist, 19(6), 649–655. DOI: https://doi.org/10.1093/geront/20.6.649