Understanding Multilevel Factors Related to Urban Community Trust in Healthcare and Research

被引:64
作者
Hooper, Monica Webb [1 ]
Mitchell, Charlene [1 ]
Marshall, Vanessa J. [1 ,2 ]
Cheatham, Chesley [1 ,2 ]
Austin, Kristina [3 ]
Sanders, Kimberly [1 ,4 ]
Krishnamurthi, Smitha [1 ,4 ]
Grafton, Lena L. [5 ]
机构
[1] Case Western Reserve Univ, Case Comprehens Canc Ctr, Cleveland, OH 44106 USA
[2] Univ Hosp Cleveland, Med Ctr, Seidman Canc Ctr, Cleveland, OH 44106 USA
[3] Gathering Pl, Beachwood, OH 44122 USA
[4] Cleveland Clin, Taussig Canc Inst, Cleveland, OH 44195 USA
[5] Cleveland State Univ, NEOMED CSU Partnership Urban Hlth, Cleveland, OH 44115 USA
关键词
community-based participatory research (CBPR); community engagement; community listening tour; distrust; healthcare; health disparities; cancer; AFRICAN-AMERICAN; PARTICIPATORY RESEARCH; RACIAL-DIFFERENCES; DISTRUST; SYSTEM;
D O I
10.3390/ijerph16183280
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Background: Community and patient engagement in the healthcare system and biomedical research are prerequisites for eliminating health disparities. We conducted a listening tour to enhance our understanding of multilevel factors associated with community trust. Methods: Using community-based participatory research (CBPR) methods, we conducted a phenomenological qualitative study. Town-hall style discussions were held at nine sites across an urban, Midwestern city. We recruited adults (N = 130) via community networks, social media, flyers, and word-of-mouth. Demographic assessments were self-administered and listening tour sessions were conducted by trained moderators. Themes were framed within the social ecological model (SEM; intrapersonal, interpersonal, institutional, community, and policy levels). Results: Participants were mostly female (68%), African American (80%), had health coverage (97%) and were diagnosed with a chronic health condition (71%). The overarching theme was sociodemographic differences in distrust, such that African Americans and deaf/hearing impaired participants perceived disparities in healthcare, a lower quality of care, and skepticism about biomedical research, relative to Whites. Conclusions: The depth of distrust for healthcare providers, systems, and researchers in underserved communities remains strong and complex. Findings highlight the need to understand the lived experiences of community members, and how distrust is maintained. Multilevel interventions to increase trust and the accrual of underrepresented populations into clinical trials are needed.
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页数:16
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