CCHD COMMUNITY CORE

CCHD 社区核心

• 批准号: 7622799
• 负责人: David Martins
• 金额: $ 24.35万
• 依托单位: CHARLES R. DREW UNIVERSITY OF MED & SCI
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-08-01 至 2008-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7622799
• 关键词: African American; Arts; Caring; Caucasians; Caucasoid Race; Chronic Kidney Failure; Communities; Computer Retrieval of Information on Scientific Projects Database; Disease Outcome; End Point; Funding; Grant; Health; Health Personnel; Health Professional; Health Promotion; Institution; Latino; Low income; Mentors; Modeling; Monitor; Outcome; Patients; Platelet Factor 4; Population; Process; Research; Research Personnel; Resources; Risk; Risk Factors; Scientist; Source; Training; Underrepresented Minority; United States National Institutes of Health; Work; base; community based participatory research; disorder risk; health disparity; improved; innovation; member; programs; skills

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Although African Americans and Latinos are disproportionately afflicted with chronic kidney disease (CKD), few participate in research. Because of this, limited information is available to guide culturally sensitive health promotion efforts and appropriate evidence-based care for these populations. African Americans and Latinos are also less likely than Caucasians to obtain important health information from health care providers or community resources. In this core, we seek to reduce these disparities by implementing community-focused participatory research and disseminating state-of-the-art health information to underserved minority communities. Few researchers are trained to carry out high-quality health disparities work in the community. Mentoring provides an important mode for training culturally sensitive researchers. In this core, we also provide mentoring opportunities to produce high-quality health disparities researchers. We will develop a reproducible model of academic/community partnerships to improve CKD outcomes through the following Specific Aims: 1) To partner with community members in CKD related research; 2) To develop, evaluate and implement innovative strategies for disseminating culturally sensitive evidence-based CKD-related health information to patients, people at risk, and health care professionals in diverse low-income communities; 3) To train and develop highly skilled, research scientists with culturally sensitive community-based participatory research skills to improve health outcomes for patients with CKD and major CKD risk factors; 4) To establish a monitoring process to evaluate ongoing program activities and the impact of the Community Core program on key endpoints.

该子项目是利用该技术的众多研究子项目之一 资源由 NIH/NCRR 资助的中心拨款提供。子项目及 研究者 (PI) 可能已从 NIH 的另一个来源获得主要资金， 因此可以在其他 CRISP 条目中表示。列出的机构是 对于中心来说，它不一定是研究者的机构。 尽管非裔美国人和拉美裔人患有慢性肾病 (CKD) 的比例较高，但很少有人参与研究。因此，可用于指导文化敏感的健康促进工作以及针对这些人群的适当循证护理的信息有限。与白种人相比，非裔美国人和拉美裔人从医疗保健提供者或社区资源获取重要健康信息的可能性也较小。 在这个核心中，我们寻求通过实施以社区为中心的参与性研究并向服务不足的少数族裔社区传播最先进的健康信息来减少这些差异。很少有研究人员接受过培训，能够在社区开展高质量的健康差异工作。指导为培养具有文化敏感性的研究人员提供了重要模式。 在此核心方面，我们还提供指导机会来培养高质量的健康差异研究人员。 我们将开发一个可复制的学术/社区伙伴关系模型，通过以下具体目标改善 CKD 成果： 1) 与社区成员合作进行 CKD 相关研究； 2) 制定、评估和实施创新战略，向不同低收入社区的患者、高危人群和医疗保健专业人员传播文化敏感、循证的 CKD 相关健康信息； 3) 培训和培养具有文化敏感的社区参与性研究技能的高技能研究科学家，以改善 CKD 患者和主要 CKD 危险因素的健康结果； 4) 建立监测流程，以评估正在进行的计划活动以及社区核心计划对关键终点的影响。