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Cervicogenic headache treated by acupuncture based on jin theory: study protocol for a randomized controlled trial

机译:基于金理论治疗针灸治疗的宫颈癌:随机对照试验的研究方案

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摘要

Numerous randomized trials involving acupuncture treatment for cervicogenic headache (CEH) have been conducted in recent years, but the evidence for its effectiveness is not clear. Hence, we designed a randomized trial to evaluate the efficacy and advantages of acupuncture for treating CEH. This is a parallel-design, two-arm, patient-assessor blinded, randomized, sham-controlled clinical trial. A total of 166 patients with CEH aged from 18 to 70 will be recruited and assigned randomly into a jin acupuncture group and a pseudo acupuncture group at a 1:1 ratio; they will receive 12 sessions of real acupuncture and sham acupuncture for 4?weeks, respectively, during the study. The primary outcomes are pain degree (PD) and pain rate (PR) calculated by the PainVision analyzer, as well as parameters detected by surface electromyography (SEMG). The secondary outcomes will be measured with the short-form McGill Pain Questionnaire (SF-MPQ), range of motion (ROM) of the neck, the Northwick Park Neck Pain Questionnaire (NPQ), the 36-item short-form Health Survey (SF-36), the Self-Rating Anxiety Scale (SAS), and the Self-Rating Depression Scale (SDS). Clinical assessments will be evaluated at baseline and in the fourth week as well as in the eighth and sixteenth weeks. Adverse events will be noted and recorded for the safety evaluation. This study will provide high-quality evidence of the value of acupuncture based on jin theory for treating CEH. Chinese Clinical Trial Registry, ChiCTR1800015316 . Registered on 22 March 2018. Updated version AMCTR-IOR-18000157 . Registered on 1 April 2018.
机译:近年来进行了涉及针灸治疗针灸治疗的多种随机试验,但其有效性的证据尚不清楚。因此,我们设计了一种随机试验,以评估针灸治疗CEH的功效和优点。这是一个平行设计,双臂,患者评估仪盲,随机,假控临床试验。将招募166例CEH患者18至70岁,将随机募集和分配给Jin针灸组和1:1的伪针灸组;在研究期间,他们将分别收到12个真正的针灸和假针灸4?周数。主要结果是由止痛感分析仪计算的疼痛程度(PD)和疼痛率(PR),以及由表面肌电图(SEMG)检测的参数。次要结果将用短麦吉尔疼痛问卷(SF-MPQ),颈部的运动范围(ROM),北威克公园颈部疼痛问卷(NPQ),36项短态健康调查( SF-36),自评焦虑尺度(SAS)和自评抑郁尺度(SDS)。临床评估将在基线和第四周以及第八和第十六周内进行评估。将注意到不良事件并记录安全评估。本研究将提供基于JIN理论治疗CEH的针灸价值的高质量证据。中国临床试验登记处,CHICTR1800015316。 2018年3月22日注册。更新版本AMCTR-IOR-18000157。 2018年4月1日注册。

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