Implementation of a Theory-based, Non-clinical Patient Navigator Program to Address Barriers in an Urban Cancer Center Setting.

Linda Fleisher, Suzanne M Miller, Danielle Crookes, Venk Kandadai, Kuang Yi Wen, Rachel E Slamon, Jeanne Chaivous
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Abstract

Cancer patients face a myriad of psychosocial and practical issues. Especially challenging is the time from an initial diagnosis to the onset of treatment and patient navigation services are important to guide patients, especially underserved populations, through this maze of uncertainty. Here we report on the Pennsylvania Patient Navigator Demonstration Project (PaPND) designed to evaluate the acceptability, feasibility, and impact of a culturally and linguistically appropriate non-clinical navigator program. The development of the project, based on behavioral theory and community-based participatory research principles, is described. Forty-four cancer patients from diverse backgrounds participated, which included a baseline assessment, navigation services, and a four week and twelve week follow-up assessment. On average, participants experienced 1.8 barriers with transportation and insurance issues the most common barriers. The majority (56%) of the barriers required more than an hour of the navigator's time to address, with insurance, transportation and caregiver/support issues requiring the most time. Overall patients were fairly satisfied with the navigation services. The findings showed improvement patient's stress-related thoughts, cognition (understanding of their disease), expectancies and beliefs or values/goals, as well as self-efficacy of managing cancer related issues from the baseline to follow-up assessments. The evaluation results suggest that providing and connecting cancer patients to appropriate information to improve their understanding of their diagnosis and recommended treatments needs to be addressed, and where the integration of non-clinical and clinical navigation is essential. In addition, more attention to the assessment of psychosocial issues, such as the patients' emotional worries, and more comprehensive training in these areas would enhance navigation programs.

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实施基于理论的非临床患者导航计划,以解决城市癌症中心设置的障碍。
癌症患者面临着无数的社会心理和实际问题。尤其具有挑战性的是从最初诊断到开始治疗的时间,患者导航服务对于引导患者,特别是服务不足的人群,通过这一迷宫般的不确定性至关重要。在这里,我们报告了宾夕法尼亚州患者导航员示范项目(PaPND),旨在评估文化和语言上适当的非临床导航员计划的可接受性,可行性和影响。描述了基于行为理论和社区参与性研究原则的项目发展。44名来自不同背景的癌症患者参与了这项研究,其中包括基线评估、导航服务以及4周和12周的随访评估。参与者平均遇到1.8个障碍,其中交通和保险问题是最常见的障碍。大多数障碍(56%)需要导航员花费超过一个小时的时间来解决,其中保险、交通和护理/支持问题需要最多的时间。总体而言,患者对导航服务相当满意。研究结果显示,从基线到后续评估,患者的压力相关思想、认知(对其疾病的了解)、期望和信念或价值观/目标,以及管理癌症相关问题的自我效能都有所改善。评估结果表明,需要解决为癌症患者提供和连接适当的信息,以提高他们对诊断和推荐治疗的理解,并且非临床和临床导航的整合至关重要。此外,更多地关注心理社会问题的评估,如患者的情绪担忧,并在这些领域进行更全面的培训,将提高导航程序。
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