Mei Jinjin, Xue Yang, Li Jingwen, Zhang Lihong, Zhang Jianyun, Wang Yiying, Su Kaiqi, Gao Jing, Guo Jian, Li Ruiqing
Henan University of Chinese Medicine, Zhengzhou, China.
Rehabilitation Center, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China.
Front Neurol. 2022 May 18;13:835408. doi: 10.3389/fneur.2022.835408. eCollection 2022.
Upper limb spasticity (ULS) is a common complication after stroke, which seriously affects the quality of life and rehabilitation of patients. There are different treatment methods for post-stroke spasticity (PSS). Our group found that functional acupuncture (FA) can effectively improve forearm spasticity and hand dysfunction after stroke, but the efficacy of ULS needs to be further verified. Therefore, this subject has mainly used clinical randomized controlled trials to evaluate the clinical efficacy of FA in the treatment of ULS after ischemic stroke.
This is a parallel design and randomized controlled trial. We selected 108 patients who met the predefined criteria and randomized them into two groups, the experimental group and the control group. The experimental group receives FA and routine rehabilitation treatment. The control group received traditional acupuncture (TA) and routine rehabilitation treatment. All patients received 20 courses of treatment for 4 weeks, and the modified Ashworth score (MAS), clinical neurological deficit score (CSS), Fugl-Meyer upper extremity function assessment (FMA-UE), and the Modified Barthel Index (MBI) scores were evaluated before and after treatment.
This trial is mainly to study the clinical efficacy of FA in the treatment of ULS after ischemic stroke. It will not only provide a new idea for the clinical treatment of upper limb post-stroke spasticity (ULPSS) but also will provide effective experimental support and a theoretical basis for the clinic.
China Clinical Trials Registry No. ChiCTR2100050440. Registered on 27 August 27 2021.
上肢痉挛(ULS)是脑卒中后常见的并发症,严重影响患者的生活质量和康复效果。脑卒中后痉挛(PSS)有多种治疗方法。本研究团队发现,功能性针刺(FA)可有效改善脑卒中后的前臂痉挛和手部功能障碍,但ULS的疗效尚需进一步验证。因此,本课题主要采用临床随机对照试验来评估FA治疗缺血性脑卒中后ULS的临床疗效。
这是一项平行设计的随机对照试验。我们选取了108例符合预设标准的患者,将其随机分为两组,即试验组和对照组。试验组接受FA和常规康复治疗。对照组接受传统针刺(TA)和常规康复治疗。所有患者均接受为期4周的20个疗程治疗,治疗前后评估改良Ashworth评分(MAS)、临床神经功能缺损评分(CSS)、Fugl-Meyer上肢功能评估(FMA-UE)以及改良Barthel指数(MBI)评分。
本试验主要研究FA治疗缺血性脑卒中后ULS的临床疗效。它不仅将为脑卒中后上肢痉挛(ULPSS)的临床治疗提供新思路,还将为临床提供有效的实验支持和理论依据。
中国临床试验注册中心编号ChiCTR2100050440。于2021年8月27日注册。