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Spousal Caregiver Perspectives on a Person-Centered Social Program for Partners With Dementia

机译:配偶照顾者对痴呆症患者伴侣的以人为本的社会计划的观点

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This qualitative study explored spousal caregiver perspectives on the experience and impact of a person-centered social program for partners with dementia. Interviews with 5 caregivers and the spouses with dementia were conducted 7 to 8 months after the program ended to explore the sustained impact of the program. Interpretative phenomenological analysis was used to support in-depth exploration of interviews. Three themes emerged including benefits of the program for caregivers, initial expectations and later perspectives of caregivers about the program, and conflicting values and perspectives between caregivers and the spouses. These findings suggest participation in a person-centered social program by people with dementia benefits their caregivers, by meeting the caregivers' desire for their spouses to increase social participation and engagement in meaningful activities. Participation in the program provided a sustained benefit to one couple in particular, by encouraging the caregiver to resume arranging activities the couple once enjoyed but now had difficulty pursuing.
机译:这项定性研究探讨了配偶照顾者对以人为中心的社交计划对痴呆症伴侣的经验和影响的观点。该计划结束后的7至8个月,对5名护理人员和患有痴呆症的配偶进行了访谈,以探讨该计划的持续影响。解释性现象学分析用于支持访谈的深入探索。出现了三个主题,包括该计划对看护人的好处,对看护人对该计划的最初期望和以后的观点,以及看护人与配偶之间价值观和观点的冲突。这些发现表明,痴呆症患者通过参加以人为本的社会计划,可以满足照顾者对配偶增加社会参与和参与有意义的活动的愿望,从而使他们的照顾者受益。参加该计划特别是通过鼓励看护人重新安排这对夫妇曾经享受过但现在却难以进行的活动,为一对夫妇带来了持续的利益。

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