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针刺结合经颅直流电刺激治疗中国脑卒中后肩痛患者的随机对照试验方案。

Investigating combined acupuncture and transcranial direct current stimulation in patients with poststroke shoulder pain from China: protocol for a randomised controlled trial.

机构信息

Rehabilitation Hospital affiliated to Fujian University of Traditional Chinese Medicine, Fuzhou, China.

Fujian Key Laboratory of Rehabilitation Technology, Fuzhou, China.

出版信息

BMJ Open. 2024 Sep 10;14(9):e083986. doi: 10.1136/bmjopen-2024-083986.

Abstract

INTRODUCTION

Poststroke shoulder pain is a common complication that severely affects the recovery of upper limb motor function. Acupuncture has positive analgesic effects in treating poststroke shoulder pain, and studies have demonstrated the efficacy of transcranial direct current stimulation (tDCS) in treating patients with this pain. However, whether acupuncture combined with tDCS has a superior rehabilitation effect on poststroke shoulder pain is currently unknown. We aimed to observe the effect of the combined intervention on poststroke shoulder pain and explore its possible central analgesic mechanism.

METHODS AND ANALYSIS

This study describes a randomised controlled trial using assessor blinding. A total of 135 poststroke patients with shoulder pain will be randomly assigned in a 1:1:1 ratio to the tDCS group, acupuncture group and combined group (acupuncture plus tDCS). All three groups will undergo conventional rehabilitation treatment. Participants in the tDCS group will receive tDCS stimulation on the M1 area for 20 min, while the acupuncture group will receive 20 min of acupuncture. The combined treatment group will receive both. All treatments will be performed five times per week for 4 weeks. The primary outcome indicator in this study is the Visual Analogue Scale pain score. Secondary outcome indicators include shoulder mobility, Shoulder Pain and Disability Index, Fugl-Meyer Motor Function Scale, Modified Barthel Index Scale, Self-Rating Anxiety and Depression Scale and functional MRI. All scale results will be assessed at baseline and at 2 weeks and 4 weeks, and during follow-up at 1 month, 3 months and 6 months postdischarge. A repeated analysis of variance will be conducted to observe the group×time interaction effects of the combined intervention. Moreover, functional MRI will be applied to explore the central analgesic mechanism.

ETHICS AND DISSEMINATION

Ethics approval was obtained from the Ethics Committee of the Affiliated Rehabilitation Hospital of Fujian University of Traditional Chinese Medicine (2023KY-039-001). The results of the study will be published in a peer-reviewed journal and presented at scientific conferences.

TRIAL REGISTRATION NUMBER

ChiCTR2300078270.

摘要

简介

脑卒中后肩痛是一种常见的并发症,严重影响上肢运动功能的恢复。针刺在治疗脑卒中后肩痛方面具有积极的镇痛作用,研究表明经颅直流电刺激(tDCS)在治疗此类疼痛方面具有疗效。然而,针刺联合 tDCS 是否对脑卒中后肩痛具有更优的康复效果目前尚不清楚。本研究旨在观察联合干预对脑卒中后肩痛的效果,并探讨其可能的中枢镇痛机制。

方法和分析

这是一项采用评估者设盲的随机对照试验。共纳入 135 例脑卒中后伴肩痛患者,按 1:1:1 的比例随机分配至 tDCS 组、针刺组和联合组(针刺联合 tDCS)。三组患者均接受常规康复治疗。tDCS 组患者接受 M1 区 20 分钟 tDCS 刺激,针刺组患者接受 20 分钟针刺治疗,联合治疗组患者同时接受这两种治疗。所有治疗每周进行 5 次,共 4 周。本研究的主要结局指标为视觉模拟评分(VAS)疼痛评分。次要结局指标包括肩活动度、肩痛和残疾指数、Fugl-Meyer 运动功能量表、改良巴氏指数量表、焦虑和抑郁自评量表以及功能磁共振成像(fMRI)。所有量表结果将在基线时以及治疗后 2 周和 4 周进行评估,并在出院后 1 个月、3 个月和 6 个月进行随访。采用重复方差分析观察联合干预的组间×时间交互效应。此外,将应用 fMRI 来探索中枢镇痛机制。

伦理和传播

本研究已获得福建中医药大学附属康复医院伦理委员会的批准(2023KY-039-001)。研究结果将发表在同行评议的期刊上,并在科学会议上进行报告。

试验注册号

ChiCTR2300078270。

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