Efficacy of acupuncture on upper limb dysfunction after stroke: a randomized controlled trial protocol with surface electromyography evaluation.

IF 3.1 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Frontiers in Medicine Pub Date : 2025-07-10 eCollection Date: 2025-01-01 DOI:10.3389/fmed.2025.1615762
Liying Wang, Zining Guo, Jiewen Zhang, Run Lin, Xiaorong Tang, Cui Gao, Shaoyang Cui, Nenggui Xu
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引用次数: 0

Abstract

Background: Upper extremity functional reconstruction remains a major clinical challenge in post-stroke neurorehabilitation. Acupuncture has unique advantages as a complementary alternative therapy. Thus, in this study, we aim to compare sham acupuncture to reveal the efficacy and safety of acupuncture in the treatment of upper limb dysfunction post-stroke with surface electromyography (sEMG), a validated objective assessment tool, and a subjective index.

Methods: In this prospective, principal-investigator-blinded randomized controlled trial, 74 patients who meet the inclusion criteria are randomly assigned to the acupuncture and sham acupuncture groups in a 1:1 ratio using a central randomization system. The patients receive the same routine basic treatment. The core acupoints selected in the acupuncture group are GV20 (Bai hui), DU14 (Da zhui), and LI11 (Qu chi). Six non-meridian acupuncture points are selected for the sham acupuncture group. The treatment cycle lasts for 4 weeks, five times per week, for 20 treatments. The Fugl-Meyer Upper Limb Assessment scale score is used as the main outcome. Secondary outcomes include the Motor Status Scale, Action Research Arm Test, Motor Assessment Scale, Self-rating Anxiety Scale, and Self-rating Depression Scale scores. Simultaneously using sEMG as an auxiliary efficacy indicator.

Conclusion: This study assesses the effectiveness and safety of acupuncture for post-stroke upper limb impairment in multiple aspects and elucidates the underlying neuromuscular effect mechanism of acupuncture to provide clinical evidence.

Registration: International Traditional Medicine Clinical Trials Registry. Registration No. ITMCTR2025000228. November 27, 2024. The study was approved by the Ethics Committee of Guangzhou University of Traditional Chinese Medicine, Shenzhen Hospital (Futian), Ethics. No. GZYLL (KY)-2024-045-01. November 13, 2024.

针刺对中风后上肢功能障碍的疗效:一项随机对照试验方案与表面肌电图评估。
背景:上肢功能重建仍然是脑卒中后神经康复的主要临床挑战。针灸作为一种补充替代疗法具有独特的优势。因此,在本研究中,我们的目的是通过比较假针灸,以揭示针灸治疗中风后上肢功能障碍的有效性和安全性,这是一种经过验证的客观评估工具,也是一种主观指标。方法:在这项前瞻性、主要研究者盲法随机对照试验中,74例符合纳入标准的患者采用中央随机化系统,按1:1的比例随机分配到针灸组和假针灸组。患者接受相同的常规基本治疗。针刺组选取的核心穴位为GV20(白会)、DU14(大椎)、LI11(曲池)。假针组选择非经络穴位6个。治疗周期为4 周,每周5次,共20次。Fugl-Meyer上肢评估量表得分作为主要结果。次要结果包括运动状态量表、动作研究臂测试、运动评估量表、焦虑自评量表和抑郁自评量表得分。同时使用肌电图作为辅助疗效指标。结论:本研究从多个方面评价针刺治疗脑卒中后上肢功能障碍的有效性和安全性,阐明针刺的神经肌肉作用机制,为临床提供依据。注册:国际传统医学临床试验注册。没有注册。ITMCTR2025000228。2024年11月27日。本研究经广州中医药大学伦理委员会、深圳医院(福田)伦理委员会批准。否。GZYLL(肯塔基州)2024-045-01。2024年11月13日。
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来源期刊
Frontiers in Medicine
Frontiers in Medicine Medicine-General Medicine
CiteScore
5.10
自引率
5.10%
发文量
3710
审稿时长
12 weeks
期刊介绍: Frontiers in Medicine publishes rigorously peer-reviewed research linking basic research to clinical practice and patient care, as well as translating scientific advances into new therapies and diagnostic tools. Led by an outstanding Editorial Board of international experts, this multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. In addition to papers that provide a link between basic research and clinical practice, a particular emphasis is given to studies that are directly relevant to patient care. In this spirit, the journal publishes the latest research results and medical knowledge that facilitate the translation of scientific advances into new therapies or diagnostic tools. The full listing of the Specialty Sections represented by Frontiers in Medicine is as listed below. As well as the established medical disciplines, Frontiers in Medicine is launching new sections that together will facilitate - the use of patient-reported outcomes under real world conditions - the exploitation of big data and the use of novel information and communication tools in the assessment of new medicines - the scientific bases for guidelines and decisions from regulatory authorities - access to medicinal products and medical devices worldwide - addressing the grand health challenges around the world
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