Knecht Hanna L, Rodriguez Francisca S
German Center for Neurodegenerative Diseases (DZNE), RG Psychosocial Epidemiology & Public Health, Ellernholzstr. 1-2, 17489, Greifswald, Germany.
BMC Geriatr. 2025 Mar 27;25(1):202. doi: 10.1186/s12877-025-05850-8.
Social interactions can have a beneficial effect on people with dementia (PWD). However, little is known about the details of social interactions in dementia, information that is useful for planning social interventions. The aim of our study was to gain a deeper insight, provided by people in dementia care, into (i) the characteristics of social interactions of PWD, (ii) which social interactions are considered as particularly important, (iii) how important social interactions are perceived, and (iv) what is perceived to increase social interactions among PWD.
Responses of 501 people in dementia care (mostly family and professional caregivers; more than three-quarters female; average age 53.5 years) provided in a structured, quantitative survey were included in this analysis. Descriptive analyses were conducted.
The majority of PWDs' social interactions take place in their home or day care and arise from support services as well as organized activities. More than half of the participants perceived singing, telling life stories, or moving together (e.g., walking, dancing) as valuable social interactions that PWD benefit from in many ways. Positive effects (e.g., aggression, depression, positive emotions, activation) are mainly perceived for social interactions such as laughing together, touch, hugging, simply being together, or being involved in daily activities. Overall, participants rated social interactions as rather important for the course of the symptoms. A fixed social contact besides the primary caregiver and offers from the community, associations, and religious institutions are considered rather important in increasing the social interactions of PWD.
Simple social interactions of PWD such as laughing, eating or singing together that can be realized in the home environment and in the context of organized caregiving activities are perceived most valuable. Enhancing social interactions, especially beyond the primary caregiving context, may be valuable for those living with dementia.
社交互动对痴呆症患者有益。然而,对于痴呆症患者社交互动的细节了解甚少,而这些信息对于规划社会干预措施很有用。我们研究的目的是通过痴呆症护理人员更深入地了解:(i)痴呆症患者社交互动的特征;(ii)哪些社交互动被认为特别重要;(iii)社交互动被认为有多重要;(iv)人们认为什么能增加痴呆症患者的社交互动。
本分析纳入了在一项结构化定量调查中501名痴呆症护理人员(主要是家庭和专业护理人员;四分之三以上为女性;平均年龄53.5岁)的回答。进行了描述性分析。
大多数痴呆症患者的社交互动发生在他们家中或日托中心,源于支持服务以及有组织的活动。超过一半的参与者认为唱歌、讲述生活故事或一起活动(如散步、跳舞)是有价值的社交互动,痴呆症患者能从这些互动中在很多方面受益。主要在诸如一起欢笑、触摸、拥抱、仅仅在一起或参与日常活动等社交互动中感受到积极影响(如攻击性、抑郁、积极情绪、活跃度)。总体而言,参与者认为社交互动对症状发展相当重要。除了主要照顾者之外的固定社交联系以及社区、协会和宗教机构提供的活动在增加痴呆症患者社交互动方面被认为相当重要。
痴呆症患者简单的社交互动,如一起欢笑、吃饭或唱歌,这些能在家庭环境和有组织的护理活动背景下实现的互动被认为最有价值。加强社交互动,尤其是在主要护理背景之外的互动,可能对痴呆症患者有价值。