Guangdong Provincial Hospital of Chinese Medicine (The Second Affiliated Hospital of Guangzhou University of Chinese Medicine), Guangdong Provincial Academy of Chinese Medical Science, Guangzhou, Guangdong, China.
China-Australia International Research Centre for Chinese Medicine, School of Health and Biomedical Sciences, RMIT University, Melbourne, Victoria, Australia.
BMJ Open. 2019 Jul 9;9(7):e025564. doi: 10.1136/bmjopen-2018-025564.
Although acupuncture has been recommended for alleviating cancer pain by clinical guidelines, the level of the supporting evidence needs to be improved. A pragmatic randomised controlled trial (pRCT) in a hospital setting would provide real-world assessments of the overall clinical effects of acupuncture. This pilot trial aims to explore the feasibility and provide data for sample size calculations for a pRCT evaluating the effectiveness of acupuncture as an adjunctive therapy to routine medical care for cancer pain.
Thirty patients with cancer admitted to the oncology department with moderate or severe pain will be recruited. Participants will be randomised at a ratio of 1:1 to the adjunctive acupuncture group or a control group which receives routine pain management without acupuncture. The standardised section of the acupuncture protocol will be developed based on the results of reviews of the literature, recommendations in clinical guidelines and interviews with clinical experts. The acupuncturist will be allowed to tailor the protocol according to the individual situation of each participant. Primary outcomes relevant to the feasibility of conducting a fully powered trial include: numbers and proportions of participants recruited, screened, consented and randomised; numbers and reasons for withdrawals and dropouts; numbers and types of adverse events; feasibility of implementing the trial procedures; evaluation of the comprehensiveness and ease-of-use of the case report form. Secondary outcomes are clinical measurements of the effectiveness of the treatment that are intended for use in the full-scale trial. Analysis of feasibility will be descriptive and pain intensity measures will be analysed using mixed-effects regression.
Ethics approval was obtained from the Institutional Ethics Committee of Guangdong Provincial Hospital of Chinese Medicine (approval no: Z2017-184-01) and RMIT University Human Research Ethics Committee (reference no: 21361). Results will be disseminated in a peer-reviewed journal, and trial participants will be informed via email and/or phone calls.
ChiCTR1800017023.
尽管临床指南推荐针灸缓解癌痛,但支持证据的水平仍需提高。在医院环境中进行实用随机对照试验(pRCT)将提供对针灸整体临床效果的真实评估。本试验旨在探索其可行性,并为评估针灸作为常规医疗辅助治疗癌症疼痛的有效性的 pRCT 提供样本量计算数据。
将招募 30 名因中度或重度疼痛而入住肿瘤科的癌症患者。参与者将按照 1:1 的比例随机分为辅助针刺组或对照组,对照组接受常规疼痛管理而不接受针刺。基于文献回顾、临床指南建议和临床专家访谈的结果,将制定标准化的针刺方案。针灸师将根据每位参与者的个人情况调整方案。与进行全面试验可行性相关的主要结局包括:招募、筛选、同意和随机的参与者人数和比例;退出和脱落的人数和原因;不良事件的数量和类型;试验程序的实施可行性;病例报告表的全面性和易用性评估。次要结局是用于全规模试验的治疗效果的临床测量。对可行性的分析将是描述性的,疼痛强度测量将使用混合效应回归进行分析。
本研究已获得广东省中医院机构伦理委员会(批准号:Z2017-184-01)和 RMIT 大学人类研究伦理委员会(参考号:21361)的伦理批准。研究结果将在同行评议的期刊上发表,并通过电子邮件和/或电话通知试验参与者。
ChiCTR1800017023。