Negotiating the caring role and carer identity over time: 'living well' and the longitudinal narratives of family members of people with dementia from the IDEAL cohort.

IF 2.3 3区 社会学 Q2 GERONTOLOGY
Sally Stapley, Claire Pentecost, Catherine Quinn, Christina Victor, Jeanette Thom, Catherine Henderson, Isla Rippon, Serena Sabatini, Linda Clare
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Abstract

Longitudinal studies can provide insights into how family members negotiate the caring role and carer identity over time. Within longitudinal, qualitative interviews on 'living well' with dementia from the IDEAL cohort study, the aim of the analyses was to identify the shifting, embedded narratives of family members of people with dementia as they negotiated the caring role and carer identity over time. 20 semi-structured, qualitative interviews were conducted with family members of people with dementia, 14 repeated one year later, and analysed using cross-sectional and longitudinal thematic and structural narrative analyses. Longitudinal, interrelated themes, including the care needs and decline of the person with dementia, relationship change, and variable service support, framed the narrative types of family members. Six shifting narratives, apparent as dominant and secondary narrative types, characterised negotiating the caring role over time: absent/normalising, active role adoption/carer identity, resistance, acceptance and resignation, hypervigilance/submergence and role entrapment, and foreshadowed future. The presence or absence of a carer identity was also evident from interviewees' accounts, although, even where family members were overburdened by the caring role, they did not necessarily express a carer identity. Rather than considering transition into a carer identity, hearing different narratives within the caring role is important to understand how family members experience caring, whether they see themselves as 'carers', and when and how they need support. Timely and continued post-diagnostic support, where different caring narratives are recognised, is needed, as well as international initiatives for carer identification.

随着时间的推移,协商照顾角色和照顾者身份:“生活得好”和来自IDEAL队列的痴呆症患者家庭成员的纵向叙述。
纵向研究可以深入了解家庭成员如何随着时间的推移协调照顾角色和照顾者身份。在IDEAL队列研究中,对痴呆症患者“过得好”的纵向定性访谈中,分析的目的是确定痴呆症患者的家庭成员随着时间的推移在照顾角色和照顾者身份方面的转变和嵌入叙述。对痴呆症患者的家庭成员进行了20次半结构化的定性访谈,一年后重复了14次访谈,并使用横断面和纵向主题和结构叙事分析进行了分析。纵向的、相互关联的主题,包括痴呆症患者的护理需求和衰退、关系变化和可变的服务支持,构成了家庭成员的叙事类型。随着时间的推移,六种变化的叙事,明显是主导和次要的叙事类型,其特征是:缺席/正常化,积极的角色接受/照顾者认同,抵抗,接受和放弃,高度警惕/淹没和角色陷阱,以及预示未来。从受访者的描述中也可以明显看出是否存在照顾者身份,尽管即使在家庭成员因照顾角色而负担过重的情况下,他们也不一定表现出照顾者身份。与其考虑转变为照顾者的身份,倒不如听听照顾者角色中的不同叙述,这对于了解家庭成员如何体验照顾,他们是否认为自己是“照顾者”,以及他们何时以及如何需要支持很重要。需要及时和持续的诊断后支持,在不同的护理叙述得到认可的情况下,以及在护理者识别方面的国际倡议。
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来源期刊
Ageing & Society
Ageing & Society GERONTOLOGY-
CiteScore
6.30
自引率
8.00%
发文量
144
期刊介绍: Ageing & Society is an interdisciplinary and international journal devoted to the understanding of human ageing and the circumstances of older people in their social and cultural contexts. It draws contributions and has readers from many disciplines including gerontology, sociology, demography, psychology, economics, medicine, social policy and the humanities. Ageing & Society promotes high-quality original research which is relevant to an international audience to encourage the exchange of ideas across the broad audience of multidisciplinary academics and practitioners working in the field of ageing.
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