Abstract A25: Community research navigators: The bridge to increasing ethnic minority participation in clinical research

Marisela Garcia, M. Serrano, Alejandro Fernandez, Katty Nerio, K. Ashing
{"title":"Abstract A25: Community research navigators: The bridge to increasing ethnic minority participation in clinical research","authors":"Marisela Garcia, M. Serrano, Alejandro Fernandez, Katty Nerio, K. Ashing","doi":"10.1158/1538-7755.DISP17-A25","DOIUrl":null,"url":null,"abstract":"The participation of underserved ethnic minorities in clinical research is critical to achieving progress in cancer control. Ethnic minority patient accrual in clinical trials is a formidable challenge that requires patient trust, commitment, and overcoming of barriers. Racial and ethnic minorities make up about 40% of the United States population, yet are not well represented in research studies. Less than 10% of all patients with cancer enrolled in clinical trials are minorities. Diverse participation may lead to more generalizable results for under-represented groups, more best practices for prevention and treatment to specific minority groups, increase in knowledge and awareness of disparities about cancer, and a more accurate reflection of the United States9 increasingly diverse population. Although there is a proliferation of patient navigation programs to increase health care among the underserved, there is little known on its potential effects as a strategy to enhance minority clinical trial and biospecimen accrual. City of Hope has built a functional and sustainable program for addressing health inequity, which includes training a network of community research navigators (CRN) to address gaps in knowledge, medical mistrust, and access, and navigate participation and engagement of under-represented groups in research. The research navigator program draws from the patient navigation and promotora model and is a novel and innovative application to this approach. This approach has utility and applicability to address research participation barriers, including trust and referrals. It promises sustainability and cost effectiveness as trained CRNs can deliver the program. The Community Research Navigator (CRN) project enhances community advocates9 capacity by training community health leaders/promotoras as community research navigators (CRN) to widen the dissemination of the clinical trial and research participation enrollment for increased ethnic minority participation in clinical trials and health-related research. CRNs attended a 1-day training on clinical trials and research. The training included educating and encouraging individuals to proactively think about and discuss clinical trial participation with their family, friends, and health care providers; disseminating information about specific research studies, targeting the African and Latino communities; and referring individuals to specific biospecimen, clinical trials, and population studies. In total, we trained and mentored a team of 14 CRNs. Participants were 24-66 years old; most were female (86%), Latino (69%), and single (43%). After participating in the training, participants were more likely to correctly define HIPAA (p=.040) and the types of clinical trials (p=.038). In addition, CRNs were more likely to encourage clinical research participation among their family after the training (p=0.034). Further, we measured confidence in various domains, including: increase in confidence in describing the purpose and process of clinical research (p=0.006); educating minority communities about clinical trials (p=0.045); and providing informational workshops/forums on clinical research (p=0.046). Participants had an increase in overall confidence (p=.033). Our findings demonstrate that the CRN strategy holds promise in increasing minority participation in cancer clinical trials. It is an innovative application of the extensively studied patient navigation approach that warrants research. Future research should focus on the CRN project as a cost-effective tool for enrollment and retention of ethnic minorities in cancer clinical trials and the potential of enhancing clinical trial understanding outcomes among participants. Citation Format: Marisela Garcia, Mayra Serrano, Alejandro Fernandez, Katty Nerio, Kimlin Ashing. Community research navigators: The bridge to increasing ethnic minority participation in clinical research [abstract]. In: Proceedings of the Tenth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2017 Sep 25-28; Atlanta, GA. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2018;27(7 Suppl):Abstract nr A25.","PeriodicalId":254061,"journal":{"name":"Behavioral and Social Science","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Behavioral and Social Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1158/1538-7755.DISP17-A25","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

The participation of underserved ethnic minorities in clinical research is critical to achieving progress in cancer control. Ethnic minority patient accrual in clinical trials is a formidable challenge that requires patient trust, commitment, and overcoming of barriers. Racial and ethnic minorities make up about 40% of the United States population, yet are not well represented in research studies. Less than 10% of all patients with cancer enrolled in clinical trials are minorities. Diverse participation may lead to more generalizable results for under-represented groups, more best practices for prevention and treatment to specific minority groups, increase in knowledge and awareness of disparities about cancer, and a more accurate reflection of the United States9 increasingly diverse population. Although there is a proliferation of patient navigation programs to increase health care among the underserved, there is little known on its potential effects as a strategy to enhance minority clinical trial and biospecimen accrual. City of Hope has built a functional and sustainable program for addressing health inequity, which includes training a network of community research navigators (CRN) to address gaps in knowledge, medical mistrust, and access, and navigate participation and engagement of under-represented groups in research. The research navigator program draws from the patient navigation and promotora model and is a novel and innovative application to this approach. This approach has utility and applicability to address research participation barriers, including trust and referrals. It promises sustainability and cost effectiveness as trained CRNs can deliver the program. The Community Research Navigator (CRN) project enhances community advocates9 capacity by training community health leaders/promotoras as community research navigators (CRN) to widen the dissemination of the clinical trial and research participation enrollment for increased ethnic minority participation in clinical trials and health-related research. CRNs attended a 1-day training on clinical trials and research. The training included educating and encouraging individuals to proactively think about and discuss clinical trial participation with their family, friends, and health care providers; disseminating information about specific research studies, targeting the African and Latino communities; and referring individuals to specific biospecimen, clinical trials, and population studies. In total, we trained and mentored a team of 14 CRNs. Participants were 24-66 years old; most were female (86%), Latino (69%), and single (43%). After participating in the training, participants were more likely to correctly define HIPAA (p=.040) and the types of clinical trials (p=.038). In addition, CRNs were more likely to encourage clinical research participation among their family after the training (p=0.034). Further, we measured confidence in various domains, including: increase in confidence in describing the purpose and process of clinical research (p=0.006); educating minority communities about clinical trials (p=0.045); and providing informational workshops/forums on clinical research (p=0.046). Participants had an increase in overall confidence (p=.033). Our findings demonstrate that the CRN strategy holds promise in increasing minority participation in cancer clinical trials. It is an innovative application of the extensively studied patient navigation approach that warrants research. Future research should focus on the CRN project as a cost-effective tool for enrollment and retention of ethnic minorities in cancer clinical trials and the potential of enhancing clinical trial understanding outcomes among participants. Citation Format: Marisela Garcia, Mayra Serrano, Alejandro Fernandez, Katty Nerio, Kimlin Ashing. Community research navigators: The bridge to increasing ethnic minority participation in clinical research [abstract]. In: Proceedings of the Tenth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2017 Sep 25-28; Atlanta, GA. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2018;27(7 Suppl):Abstract nr A25.
社区研究导航员:提高少数民族参与临床研究的桥梁
让得不到充分服务的少数民族参与临床研究,对于在癌症控制方面取得进展至关重要。临床试验中少数民族患者的积累是一项艰巨的挑战,需要患者的信任、承诺和克服障碍。种族和少数民族约占美国人口的40%,但在研究中却没有得到很好的代表。在所有参加临床试验的癌症患者中,只有不到10%是少数族裔。多样化的参与可能会为代表性不足的群体带来更普遍的结果,为特定的少数群体提供更多预防和治疗的最佳实践,增加对癌症差异的知识和意识,并更准确地反映美国日益多样化的人口。尽管有大量的病人导航项目来增加服务不足人群的医疗保健,但很少有人知道它作为一种提高少数群体临床试验和生物标本积累的策略的潜在影响。希望之城为解决卫生不平等问题建立了一个功能性和可持续的项目,其中包括培训社区研究导航员(CRN)网络,以解决知识差距、医疗不信任和获取途径,并引导代表性不足的群体参与和参与研究。研究导航程序借鉴了患者导航和促进模型,是该方法的一个新颖和创新的应用。这种方法在解决研究参与障碍(包括信任和推荐)方面具有实用性和适用性。它保证了可持续性和成本效益,因为训练有素的crn可以执行该计划。社区研究导航员(CRN)项目通过培训社区卫生领导者/推动者作为社区研究导航员(CRN)来提高社区倡导者的能力,以扩大临床试验和研究参与的传播,增加少数民族参与临床试验和健康相关研究的人数。crn参加了为期1天的临床试验和研究培训。培训包括教育和鼓励个人积极思考和讨论与家人、朋友和卫生保健提供者参与临床试验;以非洲和拉丁裔社区为对象,传播有关具体研究的信息;并将个人介绍给特定的生物标本,临床试验和人口研究。我们总共培训和指导了一个由14名crn组成的团队。参与者年龄在24-66岁之间;大多数是女性(86%),拉丁裔(69%)和单身(43%)。参加培训后,参与者更有可能正确定义HIPAA (p= 0.040)和临床试验类型(p= 0.038)。此外,crn在培训后更有可能鼓励其家人参与临床研究(p=0.034)。此外,我们测量了各个领域的信心,包括:描述临床研究目的和过程的信心增加(p=0.006);对少数民族社区进行临床试验教育(p=0.045);提供临床研究信息研讨会/论坛(p=0.046)。参与者的整体信心有所增加(p= 0.033)。我们的研究结果表明,CRN策略有望增加少数族裔参与癌症临床试验。这是广泛研究的患者导航方法的创新应用,值得研究。未来的研究应将重点放在CRN项目上,将其作为一种具有成本效益的工具,用于在癌症临床试验中招募和保留少数民族,并有可能提高临床试验对参与者结果的理解。引文格式:Marisela Garcia, Mayra Serrano, Alejandro Fernandez, Katty Nerio, Kimlin ash。社区研究导航员:提高少数民族参与临床研究的桥梁[摘要]。见:第十届AACR会议论文集:种族/少数民族和医疗服务不足人群的癌症健康差异科学;2017年9月25-28日;亚特兰大,乔治亚州。费城(PA): AACR;癌症流行病学杂志,2018;27(7增刊):摘要nr A25。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信