Bajwa Rupinder, Hanjari Matilda, Al-Oraibi Amani, Akyea Ralph, Brar Manjot, Robinson Louise, Stephan Blossom C M, Qureshi Nadeem, Bains Manpreet
University of Nottingham, Nottingham, UK
University of Nottingham, Nottingham, UK.
BMJ Open. 2025 May 30;15(5):e092370. doi: 10.1136/bmjopen-2024-092370.
This study explored knowledge of dementia, attitudes towards dementia risk prediction and barriers and facilitators to accessing dementia services for diverse populations in England.
Qualitative study using task group methodology, interrogated through framework analysis.
Task groups were held primarily in-person at local community venues (n=12) with one task group conducted online.
147 individuals (mean age=63 years old, 62% female) were recruited, representing low-income and ethnically diverse groups from two sites (Nottingham and Newcastle, UK). Participants were from diverse ethnic backgrounds with 37% Black or Black British, 24% Asian or Asian British, 20% white, 9% not provided, 7% Arab and 1% other ethnicities.
Participants possessed some knowledge about dementia but highlighted a need for better access to information about dementia. Participants were knowledgeable about dementia risk factors, but knowledge of risk prediction was low. Attitudes towards dementia risk prediction were cautiously optimistic, and the use of risk prediction tools was viewed as empowering. However, participants stressed the need to consider the psychological impact of a high-risk result. Barriers to accessing dementia services included stigma, denial, language, cultural and religious views about dementia. Recommendations for service improvement included engaging with communities in their spaces, workforce training around dementia awareness, cultural competency and communicating with diverse groups, improving the provision of information in different languages and access to translators.
As international policy on dementia shifts focus to prevention, there is a growing interest in identifying those at high risk and intervening early. This study illustrates current levels of dementia knowledge and attitudes towards risk prediction among socioeconomically and ethnically diverse groups in the UK. Barriers to health services for diverse populations and service improvement recommendations offer a starting point for providers to develop culturally aware and inclusive dementia services.
本研究探讨了英格兰不同人群对痴呆症的认知、对痴呆症风险预测的态度以及获取痴呆症服务的障碍和促进因素。
采用任务组方法的定性研究,通过框架分析进行探究。
任务组主要在当地社区场所面对面进行(n = 12),有一个任务组在线进行。
招募了147名个体(平均年龄 = 63岁,62%为女性),代表来自两个地点(英国诺丁汉和纽卡斯尔)的低收入和种族多样化群体。参与者来自不同的种族背景,其中37%为黑人或英国黑人,24%为亚洲人或英国亚洲人,20%为白人,9%未提供信息,7%为阿拉伯人,1%为其他种族。
参与者对痴呆症有一定了解,但强调需要更好地获取有关痴呆症的信息。参与者了解痴呆症的风险因素,但对风险预测的了解程度较低。对痴呆症风险预测的态度谨慎乐观,使用风险预测工具被视为赋予权力。然而,参与者强调需要考虑高风险结果的心理影响。获取痴呆症服务的障碍包括耻辱感、否认、语言、关于痴呆症的文化和宗教观念。改善服务的建议包括在社区场所与社区互动、围绕痴呆症认知、文化能力以及与不同群体沟通进行工作人员培训、以不同语言提供更多信息并提供翻译服务。
随着国际痴呆症政策将重点转向预防,人们越来越关注识别高危人群并尽早进行干预。本研究说明了英国社会经济和种族多样化群体中当前的痴呆症知识水平以及对风险预测的态度。不同人群获取医疗服务的障碍和服务改进建议为提供者开发具有文化意识和包容性的痴呆症服务提供了一个起点。