REACH: The Centre for Research in Ageing and Cognitive Health, University of Exeter Medical School, University of Exeter, Exeter, United Kingdom.
College of Health, Medicine and Life Sciences, Department of Health Sciences, Brunel University London, London, UK.
Health Soc Care Community. 2022 Nov;30(6):e4594-e4604. doi: 10.1111/hsc.13863. Epub 2022 Jun 13.
This qualitative study was designed to understand the impact of social distancing measures on people with dementia and carers living in the community in England and Wales during a period of social restrictions before the COVID-19 vaccination roll-out. We conducted 12 semi-structured interviews with people with dementia aged 50-88 years, living alone or with a partner, and 10 carers aged 61-78 years, all living with the person with dementia. Three of the interviews were with dyads. Participants were recruited during November and December 2020. We used framework analysis to identify themes and elicit suggestions for potential solutions. We identified three interrelated themes. People with dementia experienced a fear of decline in capabilities or mood and attempted to mitigate this. Carers noticed changes in the person with dementia and increased caring responsibilities, and for some, a change in the relationship. Subsequently, reduced confidence in capabilities to navigate a new and hostile environment created a cyclical dilemma of re-engaging where an inability to access usual activities made things worse. People with dementia and carers experienced neglect and being alone in their struggle, alongside feeling socially excluded during the pandemic, and there was little optimism associated with the upcoming vaccine programme. People found their own solutions to reduce the effects of isolation by keeping busy and being socially active, and practising skills deemed to help reduce the progression of dementia. This and some limited local public initiatives for the general public facilitated feelings of social inclusion. This study adds understanding to existing evidence about the longer-term experience of social isolation several months into the pandemic. It highlights the importance of health and community groups and suggests how services can find ways to support, include, and interact with people with dementia and carers during and after social restrictions.
这项定性研究旨在了解在英格兰和威尔士的社区中,在 COVID-19 疫苗接种推出之前的社交限制期间,社交距离措施对 50-88 岁的独居或与伴侣居住的痴呆症患者及其照顾者的影响。我们对 12 名独自生活或与痴呆症患者共同生活的 50-88 岁的痴呆症患者以及 10 名 61-78 岁的照顾者进行了半结构化访谈。其中有 3 次访谈是针对夫妻双方的。参与者是在 2020 年 11 月和 12 月招募的。我们使用框架分析来确定主题并引出潜在解决方案的建议。我们确定了三个相互关联的主题。痴呆症患者经历了对能力或情绪下降的恐惧,并试图减轻这种恐惧。照顾者注意到痴呆症患者的变化以及增加的照顾责任,对一些人来说,关系也发生了变化。随后,对在新的敌对环境中导航的能力缺乏信心,导致重新参与的循环困境,因为无法获得通常的活动会使情况变得更糟。痴呆症患者和照顾者在疫情期间感到被忽视和孤独,感到被社会排斥,并且对即将推出的疫苗计划几乎没有乐观情绪。人们通过保持忙碌和积极参与社交活动,以及练习被认为有助于减缓痴呆症进展的技能,找到了自己的解决方案来减轻孤立的影响。这一点以及一些针对公众的有限的地方公共倡议促进了社会包容感。这项研究增加了对大流行几个月后社交隔离的长期经验的现有证据的理解。它强调了卫生和社区团体的重要性,并提出了服务如何在社交限制期间和之后为痴呆症患者及其照顾者提供支持、包容和互动的方法。