Department of Rehabilitation and Movement Science, University of Vermont, Burlington, Vermont, USA.
Department of Veterans Affairs Medical Center, Health Services Research & Development, Salt Lake City, Utah, USA.
Gerontologist. 2024 Oct 1;64(10). doi: 10.1093/geront/gnae096.
Social participation is associated with increased quality of life and well-being but declines following the onset of dementia. Informal caregivers may facilitate social participation among people with dementia. This study aims to identify characteristics of informal caregivers associated with social participation of people with dementia in valued activities.
This cross-sectional study used data from the 2011, 2015, and 2017 National Health and Aging Trends Study (NHATS) and the National Study of Caregiving. NHATS respondents with possible or probable dementia and an informal caregiver were included (N = 1,060). Respondents were asked whether they participated in each of 5 social activities during the past month. Valued activities were considered somewhat or very important. Survey-weighted logistic regression models were computed to identify characteristics of primary informal caregivers associated with participation of people with dementia in social activities.
Social participation of people with dementia was not independently associated with sociodemographic variables or relationship to the primary caregiver (spouse/partner, adult child, or other relative/nonrelative). Social participation of primary caregivers was associated with increased participation of people with dementia in the same activity for visiting friends/family (odds ratio [OR] = 1.88, p = .016), attending religious services (OR = 4.82, p < .001), and volunteering (OR = 3.25, p = .015), whereas greater caregiver external support was associated with increased participation of people with dementia in organized activities (OR = 1.37, p = .022).
Assets of informal primary caregivers found to promote social participation of people with dementia include traveling to the person with dementia's home, being socially active themselves, and utilizing support services.
社会参与与生活质量和幸福感的提高有关,但在痴呆症发作后会下降。非正式照顾者可以促进痴呆症患者的社会参与。本研究旨在确定与痴呆症患者参与有价值活动的社会参与相关的非正式照顾者的特征。
本横断面研究使用了 2011 年、2015 年和 2017 年国家健康与老龄化趋势研究(NHATS)和国家护理研究的数据。NHATS 中可能或可能患有痴呆症且有非正式照顾者的受访者被纳入(N=1060)。受访者被问及他们在过去一个月是否参加了 5 项社会活动中的每一项。有价值的活动被认为是有些或非常重要的。计算了调查加权逻辑回归模型,以确定与痴呆症患者社会参与相关的主要非正式照顾者的特征。
痴呆症患者的社会参与与社会人口统计学变量或与主要照顾者的关系(配偶/伴侣、成年子女或其他亲属/非亲属)无关。主要照顾者的社会参与与痴呆症患者参与相同活动的可能性增加有关,包括拜访朋友/家人(优势比[OR]=1.88,p=0.016)、参加宗教服务(OR=4.82,p<0.001)和志愿服务(OR=3.25,p=0.015),而照顾者获得更多外部支持与痴呆症患者参与有组织活动的可能性增加有关(OR=1.37,p=0.022)。
发现促进痴呆症患者社会参与的非正式主要照顾者的资产包括前往痴呆症患者的家、自己积极参与社交活动以及利用支持服务。