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Public engagement with cohort participants in Scotland and India: How do participants want to shape mental health research?

机译:与苏格兰和印度的队列参与者进行公众参与:参与者如何塑造心理健康研究?

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IntroductionWe now have the opportunity to disentangle the complexities of lifespan brain health through linking rich birth cohorts data to novel information utilizing health informatics techniques. Wellcome Trust evidenced that efforts to manage and link digital health data require exploring the attitudes of public and data guardians towards this initiative. Objectives and ApproachOur teams in Aberdeen, Mysore and Mumbai have established general population cohorts that have provided evidence on the early-life origins of later-life diseases. In 2016, we engaged with the participants of the Aberdeen Children of the 1950s (62-68,N~8,400) in an event attended by 350 study members. We are also engaging with members and data guardians of Mysore Parthenon Cohort (20-21y,N~500), Mysore Birth Records Cohort (51-83y,N~750), and Mumbai Maternal Nutrition Cohort (5-11y,N~1,600). This qualitative project utilises focus groups and individual interviews. The goal is to understand their attitudes and perceived public benefits towards future novel data collection, data platforms and biorepositories. ResultsThe ACONF event attendees were very willing to volunteer for further studies. The highest support was for ‘provide a blood sample’ (92%) and the lowest for ‘take an online survey’ (83%). They were satisfied with data governance but had incomplete understanding of linkage possibilities with their data. Through the ongoing activities in Mysore and in Mumbai, we aim to achieve the following: 1) Develop awareness of health informatics through public engagement with participants and researchers; 2) Explore attitudes and potential barriers to creation of secure data linkage between imaging, laboratory, health data and outcomes to facilitate future linkage studies; 3) Understand what is required for interoperable, secure data storage and plan future biorepository as a resource for researchers that will build over time in India. Conclusion/ImplicationsThe proposed activities will inform preparation of a large scale grant to investigate the hypothesis that early life environment affects future risk of mental illness and cognitive ability globally. They will also begin to create a platform of enduring value for future cross-cultural population research.
机译:简介我们现在有机会通过使用健康信息学技术将丰富的出生队列数据与新颖的信息联系起来,来解决终生大脑健康的复杂性。 Wellcome Trust证明,管理和链接数字健康数据的工作需要探索公众和数据监护人对此计划的态度。目的和方法我们在阿伯丁,迈索尔和孟买的团队建立了一般人群,这些人群为晚年疾病的早年起源提供了证据。 2016年,我们与1950年代阿伯丁儿童(62-68,N〜8,400)的参与者进行了交流,有350名研究成员参加了该活动。我们还与迈索尔帕特农神庙队列(20-21y,N〜500),迈索尔出生记录队列(51-83y,N〜750)和孟买孕产妇营养队列(5-11y,N〜1600)的成员和数据监护人合作)。这个定性项目利用焦点小组和个人访谈。目的是了解他们对于未来新颖的数据收集,数据平台和生物存储库的态度和感知的公共利益。结果ACONF活动的参与者非常愿意自愿继续学习。支持率最高的是“提供血液样本”(92%),支持率最低的是“进行在线调查”(83%)。他们对数据治理感到满意,但对与数据的链接可能性不完全了解。通过迈索尔和孟买正在进行的活动,我们的目标是实现以下目标:1)通过与参与者和研究人员的公众参与,提高对健康信息学的认识; 2)探索在成像,实验室,健康数据和结果之间建立安全数据链接的态度和潜在障碍,以促进将来的链接研究; 3)了解互操作性,安全数据存储的要求,并计划将来的生物存储库,作为将在印度随时间推移而建立的研究人员的资源。结论/意义拟议的活动将为大规模赠款的准备工作提供信息,以调查有关早期生活环境影响全球未来精神疾病风险和认知能力的假设。他们还将开始为未来的跨文化人口研究创造持久价值的平台。

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