Mobilizing morality: how caregivers in Vietnam handle the challenges of daily diabetes care

Dieu Bui Thi Huyen*, Ai Nguyen Thi, Dung Vu Thi Kim, Hieu Le Minh, Tine Gammeltoft, Amalie Rørholm Vestergaard

*Corresponding author af dette arbejde

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

1 Citationer (Scopus)
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Abstract

Background
As a chronic disease, type 2 diabetes (T2D) often involves long-term care obligations for patients’ family members. Understanding the socially and culturally specifc challenges that family caregivers face and how they
cope with them is crucial in developing targeted and efective interventions to support both caregivers and patients with T2D. This research examined family caregiving for people with T2D living in rural northern Vietnam. Although
there is a growing literature on family support in Vietnam, little is known about the personal experiences of family caregivers for people with T2D. This paper seeks to fll this gap revealing some of the challenges and coping strategies
of family caregivers to people with T2D.
Methods
This qualitative study is based on ethnographic research using primarily semi-structured interviews with 21 caregivers to a person with T2D in Vietnam. The research was conducted in 2022 by a Vietnamese-Danish research team. Each interview was voice-recorded, transcribed verbatim and thematically coded. Results
Four major challenges emerged from the analysis: physical health concerns, psychological exhaustion, economic burdens, and lack of support. Caregivers expressed motivation to overcome these challenges as they felt a deep sense of responsibility towards their family member with diabetes. The primary caregiver’s sense of responsibility toward their family would often cause them not to share the burdens from caregiving with other family members to avoid burdening them as well. However, negative experiences from caregiving were decreased and positive feelings increased in the instances where caregiving was shared between multiple family members.
Conclusion
While family members expressed motivation to take care of the patient because of moral obligations, some caregivers, specifcally primary caregivers, did not want to burden other family members with care tasks and were reluctant to ask for assistance. For families who did share the caregiving tasks among several family members, some of the negative sentiments associated with caregiving were diminished. Having multiple members of a family forming a caregiving community thus motivated people in handling care challenges.
OriginalsprogEngelsk
Artikelnummer1744
TidsskriftBMC Public Health
Vol/bind23
Udgave nummer1
Antal sider9
ISSN1471-2458
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
We are grateful to the Danish Ministry of Foreign Affairs for funding this study; to health authorities and health care staff in Thái Bình province for facilitating our work; and to the VALID research team. Lastly, we convey our heartfelt gratitude to research participants for taking part in this study

Funding Information:
The research presented in this article was funded by DANIDA, the Danish Ministry of Foreign Affairs (grant no. 17-M09-KU).

Publisher Copyright:
© 2023, BioMed Central Ltd., part of Springer Nature.

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