Belief in Research, Religious Coping, and Willingness to Participate in Clinical Trials Among African American Patients With Hematologic Malignancies: A Pilot Study

Marjorie Petty, C. Chernecky, Irina Shishkina, Nita J. Maihle, Jean D. Pawl, J. Waller, L. Young, J. Zadinsky
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Abstract

The African American (AA) population has a higher incidence and inferior outcomes in most hematologic malignancies when compared to the non- Hispanic White population. The AA population remains grossly underrepresented in clinical trials, yet few studies have evaluated the underrepresentation in the context of belief in research and willingness to participate in clinical trials. The objectives of this study were to determine if a relationship exists between belief in research and willingness to participate, and to assess the feasibility of recruiting AA patients with hematologic malignancies for cancer clinical trials. The study recruited 31 patients with acute leukemia, lymphoma, myelodysplastic syndrome, and multiple myeloma. Questionnaires were used to assess belief in research, religious coping, and willingness to participate. An oncology nurse navigator assisted with recruitment, obtaining consent, and data collection. Study results showed that 63% of participants believed in clinical trials and were willing to participate, and 74% were not informed of clinical trials. A significant association between education and belief in research (P = .01) was observed, yet no relationship was found between belief in research and willingness to participate. Further studies are warranted to investigate the obstacles to clinical trial participation among this population.
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研究信仰、宗教应对和非裔美国恶性血液病患者参与临床试验的意愿:一项初步研究
与非西班牙裔白人相比,非洲裔美国人(AA)在大多数血液学恶性肿瘤中的发病率更高,预后较差。AA人群在临床试验中的代表性仍然严重不足,但很少有研究评估在研究信念和参与临床试验意愿的背景下代表性不足。本研究的目的是确定对研究的信念与参与意愿之间是否存在关系,并评估招募血液恶性肿瘤AA患者进行癌症临床试验的可行性。该研究招募了31例急性白血病、淋巴瘤、骨髓增生异常综合征和多发性骨髓瘤患者。调查问卷用于评估对研究的信仰、宗教应对和参与意愿。肿瘤学护士导航员协助招募、获得同意和数据收集。研究结果显示,63%的参与者相信临床试验并愿意参与,74%的参与者不知道临床试验。教育程度与研究信念之间存在显著的关联(P = 0.01),但研究信念与参与意愿之间没有关系。需要进一步的研究来调查这些人群参与临床试验的障碍。
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