External Resources and Dissemination Core

外部资源和传播核心

• 批准号: 10445254
• 负责人: Matthew A Davis
• 金额: $ 20.75万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-08-01 至 2025-06-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10445254
• 关键词: Algorithms; Alzheimer' s Disease; Alzheimer' s disease related dementia; Censuses; Code; Cognitive; Communities; Complex; Data; Data Aggregation; Data Set; Data Sources; Databases; Dementia; Economics; Elderly; Ensure; Environment; Fostering; Geography; Gold; Health; Health Care Research; Health Surveys; Health and Retirement Study; Health system; Healthcare; Impaired cognition; Interview; Learning; Light; Measures; Medicare; Methodology; Michigan; Monitor; Outcome; Outcome Study; Outcomes Research; Performance; Population Research; Public Policy; Publications; Research; Research Personnel; Research Training; Resources; Series; Services; Surveys; Time; Training; Training Activity; Training Support; Universities; Work; analytical tool; care delivery; care outcomes; cognitive function; cohort; community-level factor; data access; data archive; data centers; data reuse; design; innovation; interest; multidisciplinary; podcast; population based; research and development; social; tool; virtual; web site; webinar

Project Abstract (Research Resources Core) The Research Resources Core (RRC) will support the overarching objective of the CAPRA to accelerate and expand multidisciplinary population-based AD/ADRD research by the development of robust research resources. This core will be dedicated to advancing large population-based research using a variety of rich secondary data sources in order to uncover and shed light on the complex and intertwined social, economic, and health systems effects of AD/ADRD. However, undertaking such analyses requires that researchers understand and surmount specific challenges, including: identifying relevant cohorts of older adults with demonstrated cognitive decline and/or dementia; monitoring short-term and long-term outcomes; and appreciating the local care-delivery environment. Through this core, we will package, create, and facilitate access to databases that help researchers identify relevant cohorts, outcomes of interest, and community factors—to help lower the barriers to their entry to the AD/ADRD research community. Data sources for AD/ADRD research that will be leveraged include Medicare administrative and assessment data, the Health and Retirement Study, the Michigan Long-term Services & Supports Data Archive and relevant publicly available population-based national health surveys. Research-identifiable Medicare and assessment data is both expensive to acquire and requires considerable analyst training; therefore, research with such data are often out-of-reach for researchers. However, simply facilitating access for researchers to Medicare and other large, complex health and healthcare datasets is not sufficient to ensure researchers can conduct rigorous and impactful research, particularly among early stage researchers or those new to AD/ADRD research. In this core, we will lower barriers and make high-quality data functionally accessible to AD/ADRD researchers by providing training products, aggregate data, and algorithms relevant to the field. In doing so, the RRC will also develop and disseminate a series of innovative research training activities, including the Current Topics in Dementia and Alzheimer’s Disease Research podcast & blog (the “CAPRAcast”) and a webinar series devoted to training AD/ADRD researchers (the “CAPRAclass”). We will leverage the expansive, multidisciplinary AD/ADRD research expertise at the University of Michigan and partnered external collaborators to develop resources necessary to support a wide array of AD/ADRD research. The RRC will support and foster multidisciplinary, population-based AD/ADRD research by the development of rigorous AD/ADRD-specific training, the creation and dissemination of research tools, and the provision of access to high-quality data. In this way the core will work synergistically with the other CAPRA cores by providing robust AD/ADRD research resources and training that support the overarching center aims.

项目摘要（研究资源核心） 研究资源核心（RRC）将支持CAPRA的总体目标， 通过开展强有力的研究，扩大基于人群的多学科AD/ADRD研究 资源该核心将致力于利用各种丰富的技术， 二次数据来源，以揭示和阐明复杂和相互交织的社会，经济， AD/ADRD对健康系统的影响然而，进行这种分析需要研究人员 了解和克服具体挑战，包括：确定老年人的相关群体， 表现出认知能力下降和/或痴呆;监测短期和长期结果;以及 欣赏当地的护理环境。通过这个核心，我们将包装、创造、促成 访问数据库，帮助研究人员识别相关队列、感兴趣的结果和社区 这些因素有助于降低他们进入AD/ADRD研究社区的障碍。数据源 将被利用的AD/ADRD研究包括医疗保险管理和评估数据，健康 和退休研究，密歇根州长期服务和支持数据档案和相关的公开 现有的基于人口的国家健康调查。研究可识别的医疗保险和评估数据是 获取这些数据的成本很高，而且需要大量的分析师培训;因此， 通常是研究人员无法企及的。然而，仅仅是方便研究人员获得医疗保险和其他 大型、复杂的健康和医疗保健数据集不足以确保研究人员能够进行严格和 有影响力的研究，特别是在早期阶段的研究人员或那些新的AD/ADRD研究。在这 核心，我们将降低障碍，使高质量的数据功能访问AD/ADRD研究人员， 提供与该领域相关的培训产品、汇总数据和算法。为此，RRC还将 开发和传播一系列创新的研究培训活动，包括当前的主题， 痴呆症和阿尔茨海默病研究播客和博客（“CAPRAcast”）和一个网络研讨会系列专门 培训AD/ADRD研究人员（“CAPRA班”）。我们将利用广泛的，多学科的 密歇根大学的AD/ADRD研究专业知识，并与外部合作者合作开发 支持广泛的AD/ADRD研究所需的资源。RRC将支持和促进 多学科，基于人群的AD/ADRD研究，通过开发严格的AD/ADRD特异性 培训、创建和传播研究工具以及提供获取高质量数据的途径。在 通过这种方式，该核心将与CAPRA的其他核心协同工作，提供强大的AD/ADRD研究 支持中心总体目标的资源和培训。