Relationship quality perceived by family caregivers of people with dementia in the context of a psychoeducational intervention: A qualitative exploration.

Dementia (London, England) Pub Date : 2024-11-01 Epub Date: 2024-08-06 DOI:10.1177/14713012241264611
Stephanie Kipfer, Cedric Mabire, Jean Vézina, Andrea Koppitz, Sandrine Pihet
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Abstract

Background: Caring for a person with dementia can be a challenging experience, often associated with chronic stress and a heavy burden on family caregivers. Dementia also impacts the relationship between the caregiver and the person with dementia. The quality of this relationship is, in turn, an important factor influencing the well-being of both dyad members. The psychoeducational intervention "Learning to feel better . . . and help better" has shown positive results regarding family caregivers' subjective burden, psychological distress, and self-efficacy. However, relationship quality has not been addressed in the context of this intervention.

Methods: A longitudinal constructivist grounded theory approach was used to explore relationship quality as perceived by caregivers, possible changes and intervention components facilitating or preventing such changes. Three qualitative, semi-structured interviews (before, during and after the intervention) were performed with 13 family caregivers from three different intervention groups. The resulting 39 interviews were analysed regarding individual caregiver trajectories, per time point for all caregivers and regarding specific caregiver subgroups.

Findings: A model focusing on sustaining relationship quality in dementia was developed. It shows strategies that family caregivers develop and apply to facilitate positive interactions and feelings of connectedness with their family members with dementia. It also indicates that mastering such strategies requires reflective skills based on specific knowledge of dementia and coping strategies, which can be enhanced through active skills training, in which caregivers are guided to work on their individual stressful situations. Factors hampering change included difficulties in accepting dementia-related changes.

Conclusion: Findings suggest that psychoeducation, with active skills training based on caregivers' current daily life situations, providing systematic procedures to handle daily challenges and specific knowledge about the impact of the disease, could support them in developing and applying supportive strategies to sustain or improve their relationship to their family member with dementia.

痴呆症患者家庭照顾者在心理教育干预中感知到的关系质量:定性探索。
背景介绍照顾痴呆症患者是一种极具挑战性的经历,通常会给家庭照顾者带来长期的压力和沉重的负担。痴呆症还会影响照顾者与痴呆症患者之间的关系。这种关系的质量反过来又是影响双方成员福祉的重要因素。心理教育干预 "学会更好地感受......和更好地帮助 "对家庭照护者的主观负担、心理困扰和自我效能产生了积极的影响。然而,在该干预措施的背景下,尚未对关系质量进行研究:方法: 采用纵向建构主义基础理论方法,探讨照顾者认为的关系质量、可能发生的变化以及促进或防止这种变化的干预内容。对来自三个不同干预组的 13 名家庭照顾者进行了三次半结构式定性访谈(干预前、干预期间和干预后)。对由此产生的 39 次访谈进行了分析,内容涉及照顾者的个人轨迹、所有照顾者的每个时间点以及特定照顾者亚群:研究结果:我们建立了一个模型,重点关注痴呆症患者的关系质量。该模型显示了家庭照护者为促进与痴呆症患者家人的积极互动和联系感而开发和应用的策略。它还表明,掌握这些策略需要基于痴呆症的具体知识和应对策略的反思技能,而这些技能可以通过积极的技能培训来提高,在培训过程中,护理人员会被引导去解决他们各自的压力状况。阻碍改变的因素包括难以接受与痴呆症相关的变化:研究结果表明,根据照护者当前的日常生活情况开展心理教育和积极技能培训,提供应对日常挑战的系统程序和有关疾病影响的具体知识,可以帮助他们制定和应用支持性策略,以维持或改善他们与痴呆症家庭成员的关系。
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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