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采用定性子研究为设计和实施大麻类药物治疗晚期癌症患者症状缓解的随机对照试验提供信息。

Using a qualitative sub-study to inform the design and delivery of randomised controlled trials on medicinal cannabis for symptom relief in patients with advanced cancer.

机构信息

School of Social Science, The University of Queensland, Michie Building #9, St Lucia, QLD, 4072, Australia.

Department of Palliative and Supportive Care Mater Health Services, Mater Research-University of Queensland, Raymond Terrace, South Brisbane, QLD, Australia.

出版信息

Trials. 2022 Sep 5;23(1):752. doi: 10.1186/s13063-022-06691-1.

Abstract

BACKGROUND

Recruitment for randomised controlled trials in palliative care can be challenging; disease progression and terminal illness underpin high rates of attrition. Research into participant decision-making in medicinal cannabis randomised controlled trials (RCTs) is very limited. Nesting qualitative sub-studies within RCTs can identify further challenges to participation, informing revisions to study designs and recruitment practices. This paper reports on findings from a qualitative sub-study supporting RCTs of medicinal cannabis for symptom burden relief in patients with advanced cancer in one Australian city.

METHODS

Semi-structured qualitative interviews were conducted with 48 patients with advanced cancer, eligible to participate in a medicinal cannabis RCT (n=28 who consented to participate in an RCT; n=20 who declined). An iterative and abductive approach to thematic analysis and data collection fostered exploration of barriers and enablers to participation.

RESULTS

Key enablers included participants' enthusiasm and expectations of medicinal cannabis as beneficial (to themselves and future patients) for symptom management, especially after exhausting currently approved options, and a safer alternative to opioids. Some believed medicinal cannabis to have anti-cancer effects. Barriers to participation were the logistical challenges of participating (especially due to driving restrictions and fatigue), reluctance to interfere with an existing care plan, cost, and concerns about receiving the placebo and the uncertainty of the benefit. Some declined due to concerns about side-effects or a desire to continue accessing cannabis independent of the study.

CONCLUSIONS

The findings support revisions to subsequent medicinal cannabis RCT study designs, namely, omitting a requirement that participants attend weekly hospital appointments. These findings highlight the value of embedding qualitative sub-studies into RCTs. While some challenges to RCT recruitment are universal, others are context (population, intervention, location) specific. A barrier to participation found in research conducted elsewhere-stigma-was not identified in the current study. Thus, findings have important implications for those undertaking RCTs in the rapidly developing context of medical cannabis.

摘要

背景

姑息治疗中随机对照试验的招募可能具有挑战性;疾病进展和终末期疾病导致较高的失访率。关于药用大麻随机对照试验(RCT)中参与者决策的研究非常有限。在 RCT 中嵌套定性子研究可以发现进一步参与的挑战,为研究设计和招募实践提供信息。本文报告了一项定性子研究的结果,该研究支持在澳大利亚一个城市对患有晚期癌症的患者进行药用大麻缓解症状负担的 RCT。

方法

对 48 名符合条件的晚期癌症患者进行了半结构化定性访谈,他们有资格参加药用大麻 RCT(n=28 人同意参加 RCT;n=20 人拒绝)。采用迭代和溯因方法进行主题分析和数据收集,促进了对参与障碍和促进因素的探索。

结果

主要的促进因素包括参与者对药用大麻的热情和期望,认为药用大麻对症状管理(对自己和未来的患者)有益,特别是在用尽目前批准的药物后,而且是阿片类药物的更安全替代品。一些人认为药用大麻具有抗癌作用。参与的障碍包括参与的后勤挑战(特别是由于驾驶限制和疲劳),不愿干扰现有的治疗计划,费用,以及对接受安慰剂和受益的不确定性的担忧。一些人因担心副作用或希望继续独立于研究获得大麻而拒绝。

结论

这些发现支持对随后的药用大麻 RCT 研究设计进行修订,即取消参与者每周到医院就诊的要求。这些发现突出了在 RCT 中嵌入定性子研究的价值。虽然一些 RCT 招募的挑战是普遍存在的,但其他挑战是特定于背景(人群、干预措施、地点)的。在当前研究中没有发现研究在其他地方发现的参与障碍-耻辱感。因此,这些发现对那些在医疗大麻快速发展的背景下进行 RCT 的人具有重要意义。

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Sociol Health Illn. 2023 Nov;45(8):1709-1729. doi: 10.1111/1467-9566.13684. Epub 2023 Jun 7.

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