Occupational Transitions of Family Caregivers of Loved Ones with Dementia

IF 0.5 Q4 HEALTH CARE SCIENCES & SERVICES Internet Journal of Allied Health Sciences and Practice Pub Date : 2023-01-04 DOI:10.46743/1540-580x/2023.2197
Katherine Groezinger, Cameron Honsa, Darcey Wilkinson, Emily Simpson
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Abstract

Purpose: The primary purpose of this study was to explore how family caregivers of people with dementia experience transitions in occupations as they assume the caregiver role. Because unpaid family caregivers play a vital part in the scheme of health care, it is important to understand their supports, their perceptions of themselves as caregivers, and the impact of caregiving on relationships, identity, and physical and mental health. Many researchers have studied the effects of caregiver burden, yet minimal attention has been given to the lived experiences of caregiving on their daily roles and routines. Methods: A qualitative descriptive design was used to obtain data from eight caregivers through semi-structured interviews. Content analysis was then applied to all data. Results: The following categories were identified: 1) Benefits, which consisted of the positive experiences gained as a result of caregiving; 2) Consequences, which included the physical, mental, and emotional burdens attached to being a caregiver; and 3) Supports, which were positive resources utilized by caregivers to be both better prepared to care for their loved ones and more capable within their caregiving role. Conclusion: Findings confirm that unpaid caregivers of loved ones with dementia experience dramatic changes in many aspects of their lives. Caregivers felt a strong responsibility as a family member to provide care for their loved ones. It has been found that caregivers spend most of their time engaged in caregiver related tasks, consequently impacting their occupational balance and ability to engage in what they would like to do. Health care providers must be mindful of the changes that caregivers experience, by assisting them to increase supports, anticipate the consequences, and recognize and value the benefits.
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痴呆症患者家庭照护者的职业转变
目的:本研究的主要目的是探讨痴呆症患者的家庭照顾者在承担照顾者角色时如何经历职业转变。由于无报酬的家庭照护者在卫生保健计划中发挥着至关重要的作用,因此必须了解对他们的支持、他们对自己作为照护者的看法以及照护对关系、身份和身心健康的影响。许多研究人员研究了照顾者负担的影响,但很少有人关注照顾者的生活经历对他们的日常角色和惯例的影响。方法:采用定性描述设计,对8名护理人员进行半结构化访谈。然后对所有数据进行内容分析。结果:确定了以下类别:1)益处,包括由于护理而获得的积极体验;2)后果,包括作为照顾者所带来的身体、精神和情感负担;3)支持,这是照顾者利用的积极资源,既可以更好地照顾他们的亲人,也可以更好地履行他们的照顾角色。结论:研究结果证实,无报酬照顾痴呆症患者的人在生活的许多方面都经历了巨大的变化。照顾者感到作为家庭成员有责任照顾他们所爱的人。研究发现,照顾者的大部分时间都花在与照顾者相关的任务上,从而影响了他们的职业平衡和从事他们想做的事情的能力。卫生保健提供者必须注意照顾者所经历的变化,帮助他们增加支持,预测后果,认识和重视好处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
25.00%
发文量
18
审稿时长
35 weeks
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