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低收入和中等收入国家痴呆症研究中的患者及公众参与:南亚地区能力建设

Patient and Public Involvement for Dementia Research in Low- and Middle-Income Countries: Developing Capacity and Capability in South Asia.

作者信息

Miah Jahanara, Sheikh Saima, Francis Rachel C, Nagarajan Gayathri, Antony Sojan, Tahir Maryam, Sattar Rabia, Naz Anum, Tofique Sehrish, Billah Mostazir, Saha Sajib, Leroi Iracema

机构信息

Division of Neuroscience and Experimental Psychology, University of Manchester, Manchester, United Kingdom.

Department of Speech Language Pathology, All India Institute of Speech & Hearing, Mysuru, India.

出版信息

Front Neurol. 2021 Mar 23;12:637000. doi: 10.3389/fneur.2021.637000. eCollection 2021.

Abstract

Patient and public involvement (PPI) is an active partnership between the public and researchers in the research process. In dementia research, PPI ensures that the perspectives of the person with "lived experience" of dementia are considered. To date, in many lower- and middle-income countries (LMIC), where dementia research is still developing, PPI is not well-known nor regularly undertaken. Thus, here, we describe PPI activities undertaken in seven research sites across South Asia as exemplars of introducing PPI into dementia research for the first time. Through a range of PPI exemplar activities, our objectives were to: (1) inform the feasibility of a dementia-related study; and (2) develop capacity and capability for PPI for dementia research in South Asia. Our approach had two parts. Part 1 involved co-developing new PPI groups at seven clinical research sites in India, Pakistan and Bangladesh to undertake different PPI activities. Mapping onto different "rings" of the Wellcome Trust's "Public Engagement Onion" model. The PPI activities included planning for public engagement events, consultation on the study protocol and conduct, the adaptation of a study screening checklist, development and delivery of dementia training for professionals, and a dementia training programme for public contributors. Part 2 involved an online survey with local researchers to gain insight on their experience of applying PPI in dementia research. Overall, capacity and capability to include PPI in dementia research was significantly enhanced across the sites. Researchers reported that engaging in PPI activities had enhanced their understanding of dementia research and increased the meaningfulness of the work. Moreover, each site reported their own PPI activity-related outcomes, including: (1) changes in attitudes and behavior to dementia and research involvement; (2) best methods to inform participants about the dementia study; (3) increased opportunities to share knowledge and study outcomes; and (4) adaptations to the study protocol through co-production. Introducing PPI for dementia research in LMIC settings, using a range of activity types is important for meaningful and impactful dementia research. To our knowledge, this is the first example of PPI for dementia research in South Asia.

摘要

患者及公众参与(PPI)是公众与研究人员在研究过程中的一种积极合作关系。在痴呆症研究中,PPI确保考虑有痴呆症“亲身经历”者的观点。迄今为止,在许多痴呆症研究仍在发展的低收入和中等收入国家(LMIC),PPI并不广为人知,也未经常开展。因此,在此我们描述在南亚七个研究地点开展的PPI活动,作为首次将PPI引入痴呆症研究的范例。通过一系列PPI范例活动,我们的目标是:(1)了解与痴呆症相关研究的可行性;(2)培养南亚痴呆症研究中PPI的能力。我们的方法有两个部分。第一部分涉及在印度、巴基斯坦和孟加拉国的七个临床研究地点共同组建新的PPI小组,以开展不同的PPI活动。对应威康信托基金会“公众参与洋葱”模型的不同“圈层”。PPI活动包括规划公众参与活动、就研究方案和实施进行咨询、调整研究筛查清单、为专业人员开展痴呆症培训以及为公众参与者开展痴呆症培训项目。第二部分涉及对当地研究人员进行在线调查,以深入了解他们在痴呆症研究中应用PPI的经验。总体而言,各研究地点在痴呆症研究中纳入PPI的能力得到了显著提高。研究人员报告称,参与PPI活动增强了他们对痴呆症研究的理解,并提高了工作的意义。此外,每个研究地点都报告了其自身与PPI活动相关的成果,包括:(1)对痴呆症和研究参与的态度及行为变化;(2)向参与者介绍痴呆症研究的最佳方法;(3)分享知识和研究成果的机会增加;(4)通过共同生产对研究方案进行调整。在低收入和中等收入国家环境中,采用一系列活动类型为痴呆症研究引入PPI,对于有意义且有影响力的痴呆症研究很重要。据我们所知,这是南亚痴呆症研究中PPI的首个实例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfed/8021770/3e4fcc87262e/fneur-12-637000-g0001.jpg

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