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针刺治疗广泛性焦虑障碍:一项随机对照试验的研究方案。

Acupuncture for generalized anxiety disorder: a study protocol for a randomized controlled trial.

机构信息

The Seventh Clinical Medical College, Guangzhou University of Traditional Chinese Medicine, Shenzhen, Guangdong Province, China.

Shenzhen Bao'an Traditional Chinese Medicine Hospital, Guangzhou University of Chinese Medicine, Shenzhen, Guangdong Province, China.

出版信息

Braz J Med Biol Res. 2024 May 3;57:e13389. doi: 10.1590/1414-431X2024e13389. eCollection 2024.

DOI:10.1590/1414-431X2024e13389
PMID:38716983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11085035/
Abstract

During the COVID-19 outbreak, there was a sharp increase in generalized anxiety disorder (GAD). Acupuncture therapy has the advantages of accurate clinical efficacy, safety and reliability, few adverse reactions, and no dependence, and is gradually becoming one of the emerging therapies for treating GAD. We present a study protocol for a randomized clinical trial with the aim of exploring the mechanism of brain plasticity in patients with GAD and evaluate the effectiveness and reliability of acupuncture treatment. Transcranial magnetic stimulation (TMS) will be used to assess cortical excitability in GAD patients and healthy people. Sixty-six GAD patients meeting the inclusion criteria will be randomly divided into two groups: TA group, (treatment with acupuncture and basic western medicine treatment) and SA group (sham acupuncture and basic western medicine treatment). Twenty healthy people will be recruited as the control group (HC). The parameters that will be evaluated are amplitude of motor evoked potentials (MEPs), cortical resting period (CSP), resting motor threshold (RMT), and Hamilton Anxiety Scale (HAMA) score. Secondary results will include blood analysis of γ-aminobutyric acid (GABA), glutamate (Glu), glutamine (Gln), serotonin (5-HT), and brain-derived nerve growth factor (BDNF). Outcomes will be assessed at baseline and after the intervention (week 8). This study protocol is the first clinical trial designed to detect differences in cerebral cortical excitability between healthy subjects and patients with GAD, and the comparison of clinical efficacy and reliability before and after acupuncture intervention is also one of the main contents of the protocol. We hope to find a suitable non-pharmacological alternative treatment for patients with GAD.

摘要

在 COVID-19 疫情期间,广泛性焦虑症(GAD)的发病率急剧上升。针灸疗法具有临床疗效确切、安全可靠、不良反应少、无依赖性等优点,逐渐成为治疗 GAD 的新兴疗法之一。我们提出了一项随机临床试验的研究方案,旨在探讨 GAD 患者大脑可塑性的机制,并评估针灸治疗的有效性和可靠性。我们将使用经颅磁刺激(TMS)评估 GAD 患者和健康人群的皮质兴奋性。符合纳入标准的 66 例 GAD 患者将被随机分为两组:TA 组(针灸联合基础西药治疗)和 SA 组(假针灸联合基础西药治疗)。20 名健康人将被招募为对照组(HC)。评估参数包括运动诱发电位(MEPs)幅度、皮质静息期(CSP)、静息运动阈值(RMT)和汉密尔顿焦虑量表(HAMA)评分。次要结果将包括γ-氨基丁酸(GABA)、谷氨酸(Glu)、谷氨酰胺(Gln)、血清素(5-HT)和脑源性神经营养因子(BDNF)的血液分析。结果将在基线和干预后(第 8 周)进行评估。本研究方案是首次旨在检测健康受试者和 GAD 患者大脑皮质兴奋性差异的临床试验,也是方案的主要内容之一,比较针灸干预前后的临床疗效和可靠性。我们希望为 GAD 患者找到一种合适的非药物替代治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/11085035/34a3c90f349f/1414-431X-bjmbr-57-e13389-gf003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/11085035/710e12bfa625/1414-431X-bjmbr-57-e13389-gf001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/11085035/e005a4c97980/1414-431X-bjmbr-57-e13389-gf002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/11085035/34a3c90f349f/1414-431X-bjmbr-57-e13389-gf003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/11085035/710e12bfa625/1414-431X-bjmbr-57-e13389-gf001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/11085035/e005a4c97980/1414-431X-bjmbr-57-e13389-gf002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/11085035/34a3c90f349f/1414-431X-bjmbr-57-e13389-gf003.jpg

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