Regret in Clinical Trial Participation Among Cancer Patients.

IF 2.2 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Kayla M Baker, Lucy Andersen, Molly McHugh, Anessa M Foxwell, Qiuping Zhou, Sarah J Ratcliffe, Liming Huang, Subhash Aryal, Christine Grady, Connie M Ulrich
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引用次数: 0

Abstract

Background: This analysis examined regret from participation in cancer clinical trials (CCT) and explored associations between regret and symptom burden, symptom bother, therapeutic optimism, and the importance of spiritual beliefs. Methods: This is a secondary analysis of cross-sectional data from a study of American CCT patient-participants conducted from 2015 to 2019. Descriptive statistics, bivariate associations, and logistic regression were used to evaluate regret in this sample (n = 325). Results: About 10% of the sample reported regret. Younger age, increased symptom burden, increased symptom bother, increased severe symptoms, and a lower level of therapeutic optimism were significantly associated with regret (p < 0.05) compared to those who did not experience regret. The final regression model identified that younger age, symptom burden, and therapeutic optimism significantly predicted regret (p < 0.05). Conclusions: Understanding regret among research participants may improve CCT retention and ensure ethical research practices. Symptom experiences may play a key role in experiences of regret in CCT participation.

癌症患者参与临床试验后的后悔。
背景:这项分析研究了因参与癌症临床试验(CCT)而产生的遗憾,并探讨了遗憾与症状负担、症状困扰、治疗乐观主义以及精神信仰的重要性之间的关联。研究方法这是对2015年至2019年进行的一项美国CCT患者参与者研究的横截面数据进行的二次分析。使用描述性统计、二元关联和逻辑回归来评估该样本(n = 325)中的遗憾。结果显示约 10% 的样本报告了遗憾。与没有后悔经历的人相比,年龄较小、症状负担加重、症状困扰增加、严重症状增加以及治疗乐观程度较低与后悔有显著关联(p < 0.05)。最终的回归模型表明,年龄较小、症状负担和治疗乐观程度明显预示着后悔(p < 0.05)。结论:了解研究参与者的遗憾可以提高 CCT 的保留率,确保研究实践符合道德规范。在参与 CCT 研究的过程中,症状体验可能是造成遗憾体验的关键因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of palliative medicine
Journal of palliative medicine 医学-卫生保健
CiteScore
3.90
自引率
10.70%
发文量
345
审稿时长
2 months
期刊介绍: Journal of Palliative Medicine is the premier peer-reviewed journal covering medical, psychosocial, policy, and legal issues in end-of-life care and relief of suffering for patients with intractable pain. The Journal presents essential information for professionals in hospice/palliative medicine, focusing on improving quality of life for patients and their families, and the latest developments in drug and non-drug treatments. The companion biweekly eNewsletter, Briefings in Palliative Medicine, delivers the latest breaking news and information to keep clinicians and health care providers continuously updated.
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