针刺调节促进脑卒中后偏瘫患者功能恢复:一项多中心随机平行对照试验的研究方案

Qian-qian Sun, D. Xie, J. Tao, T. Yan, Huihua Liu, Qiang Li, Bing-tian Zhang, Junmei Xu, Xiao-Kuo He
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引用次数: 1

摘要

背景与目的:常规康复方法对脑卒中后偏瘫患者的治疗效果仍不理想。研究表明,针灸可以改善中风患者的运动功能。去迟(LI11)和足三里(ST36)是治疗脑卒中后偏瘫最常用的药物。观察针刺曲池、足三里对脑卒中后偏瘫患者神经可塑性的影响。设计:这是一项前瞻性多中心随机平行对照试验。方法:试验在十堰市太和医院、中山大学孙逸仙纪念医院和福建中医药大学康复医院进行。210例脑卒中后偏瘫患者随机分为针刺优先组、针刺延迟组、假针优先组和假针延迟组(n = 45)。在基础治疗和常规康复训练的基础上,在曲池、足三里进行针灸(针灸优先组、针灸延迟组)或假针灸(假针灸优先组、假针灸延迟组),常规康复训练前15分钟(优先)或常规康复训练后15分钟(延迟),每天1次,每次30分钟,每周5天,连续8周。患者将接受一次为期4个月的随访评估。结局指标:主要结局指标将是8周后的治疗效果,用最终简化Fugl-Meyer运动功能评分与基线评分之差计算百分比,并将该值除以基线评分。Brunnstrom分期、Barthel指数评分和电生理变化将作为次要结局指标。讨论:我们希望提供新的信息,以改善针灸与现代康复治疗联合使用的时机,并确定针灸曲池和足三里对皮质兴奋性和可塑性的影响。伦理与传播:本方案已于2013年8月26日获得中国十堰太和医院(湖北医科大学附属医院)伦理委员会批准(批准号:2014001-2)。我们将把试验结果提交给国际科学会议和同行评议的期刊。研究设计于2013年7月完成。2013年8月获得伦理批准。临床注册于2017年1月至2月进行。患者招募于2017年3月开始。后续工作将于2018年9月完成。数据分析将于2019年6月进行。试验注册:本试验已在中国临床试验注册中心注册(注册号:ChiCTR-IPR-17010490)于2017年1月20日发布,并在针灸临床试验注册中心(www.acmctr.org/index.aspx;标识符:amtr - ipr -17000038),于2017年2月7日发布。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acupuncture regulation promotes functional recovery in patients with post-stroke hemiplegia: study protocol for a multicenter randomized parallel controlled trial
Background and objectives: Effect of conventional rehabilitation methods is still not satisfactory to patients with post-stroke hemiplegia. Studies have demonstrated that acupuncture can improve motor function in stroke patients. Quchi (LI11) and Zusanli (ST36) are most commonly used in the treatment of post-stroke hemiplegia. We will observe the effects of acupuncture on neural plasticity in patients with post-stroke hemiplegia after acupuncture at Quchi and Zusanli. Design: This is a prospective multicenter randomized parallel controlled trial. Methods: The trial will be conducted in Shiyan Taihe Hospital, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, and the Rehabilitation Hospital of Fujian University of Traditional Chinese Medicine, China. A total of 210 patients with post-stroke hemiplegia will be randomized into an acupuncture priority group, acupuncture delay group, sham acupuncture priority group, and sham acupuncture delay group (n = 45). On the basis of basic treatment and conventional rehabilitation training, acupuncture (acupuncture priority group and acupuncture delay group) or sham acupuncture (sham acupuncture priority group and sham acupuncture delay group) at Quchi and Zusanli will be performed 15 minutes before conventional rehabilitation training (priority) or 15 minutes after conventional rehabilitation training (delay), once a day for 30 minutes, 5 days per week, for 8 consecutive weeks. Patients will undergo one follow-up assessment for 4 months. Outcome measures: The primary outcome measure will be the efficacy of the treatment after the 8-week period, stated as a percentage calculated by taking the difference between the final simplified Fugl-Meyer motor function score and the baseline score, and dividing this value by the baseline score. Brunnstrom stage classification, Barthel Index score, and electrophysiological changes will serve as secondary outcome measures. Discussion: We hope to produce new information leading to improved timing for the combined use of acupuncture and modern rehabilitation therapy, and identify the effects of acupuncture at Quchi and Zusanli on cortical excitability and plasticity. Ethics and dissemination: The protocols have been approved by the Ethics Committee of Shiyan Taihe Hospital (Affiliated Hospital of Hubei University of Medicine) of China (approval No. 2014001-2) on August 26th, 2013. We will submit the trial's results for presentation at international scientific meetings and to peer-reviewed journals. The study design was completed in July 2013. Ethical approval was received in August 2013. Clinical registration was conducted in January–February 2017. Patient recruitment began in March 2017. The follow-up will be completed in September 2018. Data analysis will be conducted in June 2019. Trial registration: This trial was registered in the Chinese Clinical Trial Registry (registration No. ChiCTR-IPR-17010490) on January 20th, 2017, and in the Acupuncture-Moxibustion Clinical Trial Registry (www.acmctr.org/index.aspx; identifier: AMCTR-IPR-17000038) on February 7th, 2017.
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