探索临床试验意识,信息获取和参与在澳大利亚的卵巢癌患者:一个定性研究
Natalie Williams1,2, Hayley Russell3, Bridget Bradhurst3
1Ovarian Cancer Australia, Melbourne, VIC, 3000, Australia. natalie.f.williams@curtin.edu.au.
概括
患有卵巢癌的澳大利亚妇女面临临临床试验参与的障碍. 提高意识和获取需要集中信息和量身定制的沟通,以利他主义和对试验的各种情绪为驱动.
科学领域:
- 在瘤学瘤学.
- 定性研究是指质量研究.
- 患者倡导 患者倡导
背景情况:
- 卵巢癌的诊断往往发生在晚期,导致生存率差.
- 临床试验对于改善卵巢癌患者的治疗结果和生活质量至关重要.
- 了解患者的观点对于提高临床试验参与度至关重要.
研究的目的:
- 探索澳大利亚卵巢癌患者的意识,信息获取和参与临床试验.
- 确定影响患者参与卵巢癌临床试验的障碍和促进因素.
- 收集关于开发策略的见解,以改善对卵巢癌的临床试验参与.
主要方法:
- 通过在线焦点小组和采访,进行了一项探索性定性研究.
- 参与者包括在澳大利亚被诊断患有卵巢癌的妇女.
- 数据是在2023年12月至2024年2月期间收集的,并使用归纳内容分析进行分析.
主要成果:
- 出现了五个主要主题,包括意识和参与的障碍.
- 参与者强调需要发起对话并进行个人研究以找到临床试验.
- 建议的解决方案包括一个集中的可信来源,通过可信的联系人进行沟通,以及定制信息.
- 利他主义成为参与试验的重要动机,与各种情绪反应一起.
结论:
- 定性见解为全国性卵巢癌临床试验调查提供了基础.
- 结果将指导开发有针对性的干预措施,以提高临床试验的认识和获取.
- 改善信息传播和解决患者关切对于增加参与卵巢癌研究至关重要.
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