Relationships Between Cultural Perspectives and Family Caregiver Burden in the Dementia Population.

IF 2.2
Payton Adams, David A S Kaufman
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Abstract

Dementia diagnoses are increasing in the United States, causing impairments across multiple domains of functioning. Informal care provided by family caregivers can benefit those with declining cognitive function. However, this can lead to subjective and objective caregiver burden. As the United States' population becomes more diverse, literature on these topics does not fully account for cultural characteristics. The current study examined the association between key variables including cultural identity (individualism/collectivism), coping styles, and caregiver burden. A sample of 253 family caregivers of those with dementia (ages 20-78) completed a survey through Prolific, an online research platform. Sociodemographic characteristics consisted of varying racial identities, gender identities, and socioeconomic statuses. Measures included several rating scales, and statistical analyses examined the relationships between these variables. Maladaptive and adaptive coping strategies are important to the dementia family caregiver population in relation to subjective caregiver burden, which has implications for predicting health outcomes. Results demonstrated imperative considerations in the link between individualism and subjective caregiver burden. Follow-up subgroup analyses on three demographic factors displayed supplementary informative patterns. This study is one of the first widespread explorations to move towards understanding the distinctive relationships between sociocultural characteristics of caregivers. These complexities should continue to be examined to help inform effective, yet culturally competent, community-based interventions tailored towards family caregivers managing difficulties presented by a dementia diagnosis. Findings are applicable to concrete clinical directions, and a future study could test an intervention that focuses on increasing adaptive strategies, while decreasing maladaptive strategies.

痴呆人群文化视角与家庭照顾者负担的关系
在美国,痴呆症的诊断正在增加,导致多个功能领域的损伤。家庭照顾者提供的非正式护理可以使认知功能下降的人受益。然而,这可能导致主观和客观的照顾者负担。随着美国人口变得更加多样化,有关这些主题的文献并没有充分考虑到文化特征。目前的研究考察了文化认同(个人主义/集体主义)、应对方式和照顾者负担等关键变量之间的关系。253名痴呆症患者的家庭护理人员(年龄在20-78岁之间)通过在线研究平台“多产”完成了一项调查。社会人口特征包括不同的种族认同、性别认同和社会经济地位。测量方法包括几个等级量表,统计分析检查了这些变量之间的关系。适应不良和适应性应对策略对痴呆症家庭照顾者人群在主观照顾者负担方面很重要,这对预测健康结果具有重要意义。结果表明,必须考虑个人主义和主观照顾者负担之间的联系。对三个人口统计学因素的随访亚组分析显示出补充的信息模式。这项研究是第一个广泛的探索,朝着理解照顾者的社会文化特征之间的独特关系。应继续检查这些复杂性,以帮助提供有效的、具有文化能力的、基于社区的干预措施,使家庭护理人员能够处理痴呆症诊断所带来的困难。研究结果适用于具体的临床方向,未来的研究可以测试一种专注于增加适应策略,同时减少适应不良策略的干预措施。
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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