The experience of being a spouse of a person with dementia in respect to their marital relationship in Japan

IF 2.4 3区 社会学 Q2 GERONTOLOGY Dementia-International Journal of Social Research and Practice Pub Date : 2022-06-08 DOI:10.1177/14713012221107529
Mika Musgrave-Takeda, M. Ishibashi, H. Masaki
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引用次数: 1

Abstract

Background and Purpose While the marital relationship with partners with dementia has an impact on spousal carers’ well-being, the spousal understandings or expectations of their marital relationship have not been fully identified. As the marital relationship is formed by individual backgrounds including society, culture and psychological status, the aim of this study was to identify the experience of being the spouse of a person with dementia in the context of their marital relationship. The study was conducted in Japan. Research Design To identify spousal experience of being, Heideggerian perspectives of interpretive phenomenology were applied. Study Sample Seven couples aged over 65 years, each comprising one partner with dementia who received home nursing, and their spouse participated in this study. Data Collection The couples were observed, and semi-structured interviews were conducted. Data Analysis Interpretive data analysis based on the Hermeneutic circle of Heideggerian perspectives was applied. Results In the findings, the experience of being a spouse, contextualised by spousal understandings of marital relationship, was formed through seven themes. The main context for spousal understanding of their marital relationship was helping each other as husband and wife, and this relationship was seen as natural and unchanging. It reflected on spousal potentiality of being, that is, living together indefinitely as before. Spouses tried to provide suitable care for their partners using memories while preserving a sense of identity, maintaining external relationships and accepting unanticipated internal responsibility. Conclusions In conclusion, fulfilling unmet needs could help spouses to ease intense care load, which re-acknowledges their own and their partner’s identity, and their relationship by reminiscing their past.
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在日本作为痴呆症患者配偶的婚姻关系经历
背景和目的虽然与痴呆症伴侣的婚姻关系会影响配偶照顾者的幸福感,但配偶对其婚姻关系的理解或期望尚未完全确定。由于婚姻关系是由包括社会、文化和心理状况在内的个人背景形成的,本研究的目的是在痴呆症患者的婚姻关系中确定他们作为配偶的经历。这项研究是在日本进行的。研究设计为了识别配偶的存在体验,应用了解释现象学的海德格尔视角。研究样本七对年龄在65岁以上的夫妇,每对夫妇包括一名接受家庭护理的痴呆症伴侣,以及他们的配偶参与了这项研究。数据收集对夫妇进行观察,并进行半结构化访谈。数据分析基于海德格尔解释学的解释数据分析被应用。结果在研究结果中,配偶对婚姻关系的理解所带来的作为配偶的体验是通过七个主题形成的。配偶理解婚姻关系的主要背景是作为夫妻相互帮助,这种关系被视为自然和不变的。它反映了配偶存在的潜力,即像以前一样无限期地生活在一起。配偶试图利用记忆为伴侣提供适当的照顾,同时保持身份感,维持外部关系,并接受意想不到的内部责任。结论总之,满足未满足的需求可以帮助配偶减轻紧张的护理负担,这可以通过回忆他们的过去来重新承认他们自己和伴侣的身份以及他们的关系。
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来源期刊
CiteScore
5.60
自引率
12.50%
发文量
114
期刊介绍: Dementia acts as a major forum for social research of direct relevance to improving the quality of life and quality of care for people with dementia and their families. For the first time an international research journal is available for academics and practitioners that has as its primary paradigm the lived experience of dementia.
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