Exploring patient-reported barriers to participating in proton therapy clinical trials

Anne Wilhøft Kristensen , Annesofie Lunde Jensen , Kenneth Jensen , Susanne Oksbjerre Dalton , Jeppe Friborg , Cai Grau
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Abstract

Introduction

Clinical trials lead the progress in healthcare. To ensure reliable research conclusions, it is essential to enroll diverse patient groups. Identifying and understanding patient-reported barriers to clinical trials may help enhance recruitment among diverse patient groups.

The clinical potential of proton therapy (PT) to reduce late effects is being investigated in clinical trials worldwide. Thus, for some patients, PT is only accessible by participating in clinical trials.

Individuals with smoking-related head and neck cancer (HNC) are sometimes socioeconomically deprived, leading to barriers to trial participation. This study aims to identify barriers to their participation in a randomised controlled trial (RCT) involving PT.

Method

Interviews were conducted with 14 HNC patients declining participation in an RCT involving PT. The interviews were transcribed and systematically analysed using an inductive approach identifying categories and themes.

Results

The identified barriers to RCT-participation are: (1) existential distress, which influenced participants' mental and cognitive capacities, (2) insufficient RCT-related knowledge arising from information overload during clinical consultations, (3) the wish for safety and familiarity during the treatment trajectory, particularly for participants needing accommodation during  radiotherapy, and (4) the motivation for study participation was impacted by uncertainty due to randomisation and clinical equipoise. Existential distress is identified as an overarching theme because it influences and amplifies the other three themes.

Conclusion

Existential distress is a central theme that influences and amplifies other participation barriers in PT RCTs. It affects participants' comprehension of trial information, their preference for familiar environments, and their motivation to participate in clinical trials.

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探索患者报告的参与质子治疗临床试验的障碍
引言 临床试验引领着医疗保健的进步。为确保得出可靠的研究结论,必须招募不同的患者群体。识别和了解患者报告的临床试验障碍有助于提高不同患者群体的招募率。质子治疗(PT)在减少晚期效应方面的临床潜力正在全球范围内的临床试验中进行研究。因此,对于一些患者来说,只有通过参与临床试验才能获得质子治疗。与吸烟有关的头颈癌(HNC)患者有时社会经济状况不佳,这导致了他们参与试验的障碍。本研究旨在找出他们参与涉及 PT 的随机对照试验(RCT)的障碍。研究方法对 14 名拒绝参与涉及 PT 的 RCT 的 HNC 患者进行了访谈。采用归纳法对访谈内容进行了转录和系统分析,并确定了访谈的类别和主题:(结果发现的参与 RCT 的障碍包括:(1)影响参与者心理和认知能力的存在性苦恼;(2)临床咨询过程中信息超载导致的 RCT 相关知识不足;(3)希望在治疗过程中获得安全感和熟悉感,尤其是放疗期间需要住宿的参与者;(4)随机化和临床等效性导致的不确定性影响了参与研究的动机。结论存在的痛苦是一个核心主题,它影响并放大了 PT RCT 中的其他参与障碍。它影响参与者对试验信息的理解、对熟悉环境的偏好以及参与临床试验的动机。
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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
48
审稿时长
67 days
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