黑人参与睡眠医学的策略:从三项应用社区参与性研究原则的研究中获得的经验教训。

Journal of sleep disorders & therapy Pub Date : 2023-01-01
April Rogers, Alicia Chung, Azizi Seixas, Debbie Chung, Ferdinand Zizi, Girardin Jean-Louis
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引用次数: 0

摘要

引言:与其他种族/族裔群体相比,黑人对睡眠呼吸暂停的认识、评估和治疗不成比例地低。为了解决这一健康差距,需要将黑人与OSA教育、检测和治疗依从性干预措施联系起来的沟通策略。还需要通过通信技术、社区一级的社会网络支持和临床环境中的医疗提供者吸引个人的战略。我们介绍了三项研究的经验教训,这些研究使用社区参与的研究模式提供了这些解决方案:代谢综合征结局研究(MetSO)、减少睡眠种族差异的同伴增强教育(PEERS-ED)和量身定制的睡眠健康教育方法(TASHE),以捕捉项目的有效性和从项目成功和失败中吸取的经验教训。方法:OSA社区项目的方法包括应用OSA社区参与研究模型。该模型作为有效干预的战略指导方针,使社区参与研究并确保OSA干预的文化适宜性。与各持份者进行焦点小组、深入访谈和社区督导委员会会议。德尔菲调查用于确定高优先级疾病和条件。通过反复结合调查和焦点小组会议确定了社区障碍和需求。利益相关者团体参与了我们研究的各个方面,包括发展、传播和实施阶段,反映了一个双向的决策过程,确保考虑到双方的利益。对MetSO、PEERS-ED和TASHE研究进行了回顾,以了解项目的有效性并评估所吸取的经验教训。结果:MetSO, PEERS-ED和TASHE干预显示,社区参与策略在招募黑人人群进入临床试验中是成功的。研究小组调查了近3000名有阻塞性睡眠呼吸暂停综合症风险的黑人,并在纽约市的睡眠呼吸暂停研究中筛选了约2000人。睡眠手册分发给了1万多人。从MetSO、PEERS-ED和TASHE干预中吸取的教训表明,建立关系、建立信任、确定研究冠军、学会调整和提供参与者激励是成功招募和留住黑人参与临床试验的关键战略要素。结论:以社区为导向的框架的战略性应用确保了整个研究过程中社区的积极参与,允许更多的黑人参与临床研究,以及提高OSA的认识、诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Strategies to Engage Blacks in Sleep Medicine: Lessons Learned from Three Studies Applying Community-Based Participatory Research Principles.

Introduction: Awareness, assessment and treatment of sleep apnea are disproportionately lower among Blacks, compared to other racial/ethnic groups. To address this health disparity gap, communication strategies that connect Blacks to OSA education, detection and treatment adherence interventions are needed. Strategies that engage individuals through communication technologies, community-level social network support, and medical providers in clinical settings are also needed. We present lessons learned from three studies that offer these solutions using a community-engaged research model: The Metabolic Syndrome Outcome Study (MetSO), Peer-enhanced Education to Reduce Sleep Ethnic Disparities (PEERS-ED), and Tailored Approach to Sleep Health Education (TASHE), to capture program effectiveness and lessons learned from project successes and failures.

Methods: The methods of OSA community-based programs included the application of an OSA community-engaged research model. This model served as a strategic guideline for effective interventions to engage communities in research and ensure cultural appropriateness in OSA interventions. Focus groups, in-depth interviews and community steering committee meetings were conducted with various stakeholders. Delphi surveys were used to identify high priority diseases and conditions. Community barriers and needs were identified through iterative combinations of surveys and focus group meetings. Stakeholder groups participated in all aspects of our studies, including the development, dissemination and implementation phases, reflecting a bi-directional decision-making process that ensures the interests of both parties were considered. The MetSO, PEERS-ED and TASHE studies were reviewed to understand the effectiveness of the programs and to evaluate lessons learned.

Results: MetSO, PEERS-ED and TASHE interventions revealed that community-engaged strategies are successful in enrolling Black populations into clinical trials. The study teams reached nearly 3,000 Blacks at risk of OSA and screened about 2,000 people in sleep apnea studies in New York City. Sleep brochures were distributed to over 10,000 people. Lessons learned from MetSO, PEERS-ED and TASHE interventions revealed that building relationships, establishing trust, identifying a study champion, learning to adjust and providing participant incentives are key strategic elements for successful recruitment and retention of Blacks participations in clinical trials.

Conclusion: Strategic application of community-oriented frameworks ensures active community engagement throughout the research process, allowing for greater enrollment of Blacks in clinical studies as well as increased OSA awareness, diagnosis, and treatment.

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