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最大限度地提高美国黑人参与基于人群的糖尿病研究的程度:DIRECT项目的试点经验。

Maximizing participation by black Americans in population-based diabetes research: the Project DIRECT pilot experience.

作者信息

Burrus B B, Liburd L C, Burroughs A

机构信息

Research Triangle Institute, North Carolina 27709, USA.

出版信息

J Community Health. 1998 Feb;23(1):15-27. doi: 10.1023/a:1018718803890.

DOI:10.1023/a:1018718803890
PMID:9526723
Abstract

Diabetes and its associated complications and risk factors have a higher prevalence among blacks than whites. To reduce the burden of diabetes within the black community, research is needed to assess the behavioral, social, and environmental correlates associated with this disproportionate burden. Because of some well known instances of historical exploitation and abuse from medical and public health research conducted in black communities, this population has little enthusiasm for additional research, despite pressing health needs. This paper describes the process used to eliminate barriers and enhance trust between the target community and the researchers conducting a population survey of diabetes in Wake County, North Carolina. A community advisory board was organized to (1) review the survey instruments and methodologies, (2) identify persons from the community to serve as interviewers, and (3) promote the survey using the major local communication channels. The response rate to both the household survey and the comprehensive medical exam was 77%. Eighty-one percent of eligible black respondents completed the household exam and 80% completed the comprehensive medical exam. Advantages of building collaborative relationships between the community and research team are discussed.

摘要

糖尿病及其相关并发症和风险因素在黑人中的患病率高于白人。为了减轻黑人社区内糖尿病的负担,需要开展研究以评估与这种不成比例负担相关的行为、社会和环境因素。由于在黑人社区进行的医学和公共卫生研究中存在一些广为人知的历史剥削和虐待事件,尽管健康需求紧迫,但该人群对更多研究的热情不高。本文描述了在北卡罗来纳州韦克县开展糖尿病人群调查时,用于消除障碍并增强目标社区与研究人员之间信任的过程。组织了一个社区咨询委员会来(1)审查调查工具和方法,(2)从社区中挑选人员担任访谈员,以及(3)利用当地主要沟通渠道宣传该调查。家庭调查和综合医学检查的回复率均为77%。81%符合条件的黑人受访者完成了家庭检查,80%完成了综合医学检查。文中还讨论了社区与研究团队建立合作关系的优势。

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本文引用的文献

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The burdens of race and history on Black Americans' attitudes toward needle exchange policy to prevent HIV disease.种族和历史对美国黑人在预防艾滋病方面对针头交换政策态度的影响。
J Public Health Policy. 1993 Autumn;14(3):320-47.
2
A legacy of distrust: African Americans and medical research.不信任的遗产:非裔美国人和医学研究。
Am J Prev Med. 1993 Nov-Dec;9(6 Suppl):35-8.
3
Community research: partnership in black communities.社区研究:黑人社区中的伙伴关系。
探究患者及公众参与对健康和社会照护研究的影响:一项系统综述
Health Expect. 2014 Oct;17(5):637-50. doi: 10.1111/j.1369-7625.2012.00795.x. Epub 2012 Jul 19.
4
Reducing African-American women's sexual risk: can churches play a role?降低非裔美国女性的性风险:教会能发挥作用吗?
J Natl Med Assoc. 2006 Jul;98(7):1151-9.
5
Locus of control and HIV risk among a sample of Mexican and Puerto Rican women.墨西哥和波多黎各女性样本中的控制点与感染艾滋病毒风险
J Immigr Health. 2004 Oct;6(4):155-65. doi: 10.1023/B:JOIH.0000045253.19409.02.
6
Population-based interventions engaging communities of color in healthy eating and active living: a review.以社区为基础的干预措施,让有色人种社区参与健康饮食和积极生活:一项综述。
Prev Chronic Dis. 2004 Jan;1(1):A09. Epub 2003 Dec 15.
7
Screening for diabetes in an African-American community: the Project DIRECT experience.非裔美国人社区糖尿病筛查:DIRECT项目经验
J Natl Med Assoc. 2004 Oct;96(10):1325-31.
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Program prioritization to control chronic diseases in African-American faith-based communities.在非裔美国人基于信仰的社区中控制慢性病的项目优先级确定。
J Natl Med Assoc. 2004 Apr;96(4):524-32.
Am J Prev Med. 1993 Nov-Dec;9(6 Suppl):27-31; discussion 32-4.
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Household health interviews and minority health: the NCHS perspective.家庭健康访谈与少数族裔健康:美国国家卫生统计中心的观点
Med Care. 1980 Mar;18(3):327-35. doi: 10.1097/00005650-198003000-00007.