Gibson Kate, Robinson Louise, Bains Manpreet, Samsi Kritika, Cîrstea Ana-Maria, Brittain Katie
Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK
Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
BMJ Open. 2024 Dec 9;14(12):e092946. doi: 10.1136/bmjopen-2024-092946.
People living at home with dementia are often cared for by family members, especially those from minority ethnic groups. Many people living with dementia from minority ethnic communities face barriers to accessing formal care. However, there is a paucity of dementia research, which foregrounds diversity within minority ethnic populations. This study, conducted between July 2024 and August 2026, will explore the diverse care experiences of South Asian people living with dementia. Conducted across four sites (Newcastle, Nottingham, Birmingham and London), it aims to understand how inequalities related to ethnicity intersect with other factors (eg, gender, age and class) to shape the dementia care experiences of people living in South Asian communities and apply this learning to explore how public policy and care systems could be improved to reduce health and social inequalities.
In Newcastle, ethnographic research will be undertaken with up to 20 people living with dementia (or with memory concerns) in South Asian communities for a period of 12 months. The lengthy research period will enable a deep understanding about how experiences change as dementia progresses over time. In Nottingham and Birmingham, semi-structured interviews and/or focus groups will be conducted with up to 30 people living with dementia (or with memory concerns) in South Asian communities. This will enhance the data generated via the ethnographic research. Analysis will follow the principles of reflexive thematic analysis and will involve identifying themes and synthesising and theorising the data. Following this, findings will be reflected upon in 4-6 task groups convened in London, Nottingham and Newcastle with practitioners from health and social care, voluntary organisations or faith groups involved in dementia care. Task groups will focus on developing practical goals based on the research findings.
Ethical approval for this study has been granted by Newcastle University Faculty of Medical Sciences Ethics Committee (Reference: 2773/43721). Findings will be disseminated to academics, practitioners, policymakers and members of the public via a range of channels including conferences, peer-reviewed publications, lay reports, leaflets and non-written formats such as animated videos.
在家中患有痴呆症的人通常由家庭成员照顾,尤其是来自少数族裔群体的成员。许多来自少数族裔社区的痴呆症患者在获得正规护理方面面临障碍。然而,关于痴呆症的研究匮乏,而少数族裔群体内部的多样性是其研究重点。这项于2024年7月至2026年8月进行的研究,将探索南亚痴呆症患者的多样化护理经历。该研究在四个地点(纽卡斯尔、诺丁汉、伯明翰和伦敦)开展,旨在了解与种族相关的不平等如何与其他因素(如性别、年龄和阶级)相互交织,从而塑造南亚社区痴呆症患者的护理经历,并运用这些认识来探索如何改进公共政策和护理系统,以减少健康和社会不平等。
在纽卡斯尔,将对南亚社区中多达20名患有痴呆症(或有记忆问题)的人进行为期12个月的人种志研究。较长的研究周期将有助于深入了解随着痴呆症随时间发展,经历是如何变化的。在诺丁汉和伯明翰,将对南亚社区中多达30名患有痴呆症(或有记忆问题)的人进行半结构化访谈和/或焦点小组讨论。这将丰富通过人种志研究生成的数据。分析将遵循反思性主题分析原则,包括识别主题、综合数据并进行理论化。在此之后,将在伦敦、诺丁汉和纽卡斯尔召集4至6个任务组,与参与痴呆症护理的健康和社会护理从业者、志愿组织或宗教团体一起,对研究结果进行反思。任务组将专注于根据研究结果制定实际目标。
本研究已获得纽卡斯尔大学医学科学学院伦理委员会的伦理批准(参考编号:2773/43721)。研究结果将通过一系列渠道传播给学者、从业者、政策制定者和公众,包括会议、同行评审出版物、通俗报告、传单以及动画视频等非书面形式。