城市非裔美国癌症疼痛患者招募的挑战。

Stephanie Myers Schim, April Hazard Vallerand, Susan M Hasenau, Sheria Grice Robinson
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引用次数: 4

摘要

关于招募非裔美国人参与癌症研究有很多假设。人口的特点通常是年龄大,收入低,教育有限,资源稀缺,对医疗保健系统不信任。据报道,对非洲裔美国人的支持系统以家庭和教会社区为中心。在一项针对患有癌症疼痛的城市非洲裔美国人的纵向干预研究中,招募和登记的观察结果被提出。在这项研究中招募的大多数受试者都受过良好的教育,对研究知识渊博,并且对医疗保健提供者和研究人员非常开放。我们的人口比预期的要年轻,并且在家庭、信仰或社区支持的缺失中挣扎。他们在拥有手机方面联系更紧密,但由于电话服务中断、住房不安全以及与癌症医疗有关的时间需求,他们往往难以联系。我们得出的结论是,熟悉感兴趣人群的文化模式是必要的,但当地和个人评估对于成功招募研究人员至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Challenges to Recruitment of Urban African American Patients with Cancer Pain.

There are many assumptions about recruitment of African Americans to cancer studies. The population is often characterized as older, low income, with limited education, scarce resources, and distrust of the health care system. Support systems for African Americans are reported to be centered on family and church communities. Observations made during recruitment and enrollments for a longitudinal intervention study with urban African Americans with cancer pain are presented. Majority of the subjects being recruited in this study are well educated, knowledgeable about research and very open to healthcare providers and researchers. Our population is younger than anticipated and struggling with an absence of family, faith, or community supports. They are more connected in terms of phone ownership, but often difficult to contact due to interruptions in phone service, housing insecurity and time demands related to medical care for their cancer. We conclude that familiarity with cultural patterns of a population of interest is necessary, but local and individual assessment is critical to successful recruitment to research.

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