4.6 Article

Myofascial acupuncture versus routine acupuncture for mechanical neck pain: a protocol for a multicentre randomised controlled trial

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BMJ OPEN
卷 13, 期 8, 页码 -

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BMJ PUBLISHING GROUP
DOI: 10.1136/bmjopen-2022-068129

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Clinical trials; COMPLEMENTARY MEDICINE; Spine

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This study aims to compare the efficacy of myofascial acupuncture and routine acupuncture in the treatment of mechanical neck pain (MNP). The study is a multicentre, prospective randomised clinical trial involving 438 participants from four tertiary hospitals in China. The primary outcome measure is the Visual Analogue Scale score, and the secondary outcome measures include the Neck Disability Index, cervical range of motion, and MOS 36-Item Short Form Health Survey.
IntroductionMechanical neck pain (MNP) is defined as pain in the area of the neck and/or neck-shoulder provoked by body mechanics and which adversely affects physical, psychological and social function. The treatments for MNP are limited. Previous studies and clinical experience have indicated that myofascial acupuncture might be a better treatment option for MNP, but the efficacy is controversial. Therefore, our aim is to compare the efficacy of myofascial acupuncture and routine acupuncture for MNP.Methods and analysisThe study is a multicentre, prospective randomised clinical trial. Patients will be recruited from four tertiary hospitals in China. A total of 438 participants with MNP will be randomly assigned into two groups, namely the 'Sancai-Tianbu' myofascial acupuncture group and the routine acupuncture group, at a ratio of 1:1. Each group will receive the acupuncture treatment twice a week for 21 days, totalling six sessions. The primary outcome will be the Visual Analogue Scale score. The secondary outcomes will be the Neck Disability Index, the cervical range of motion and the MOS 36-Item Short Form Health Survey. The assessments will be performed at baseline (immediately after allocation), pretreatment (5 min before every treatment), post-treatment (within 10 min after every treatment), postcourse (within 1 day after the course), and at 1, 3 and 6 months after the course. All patients will be included in the intent-to-treat analysis. Repeated-measure analysis of covariance will be used to determine the effects of the intervention on the outcome measures.Ethics and disseminationEthics approval was obtained from China Aerospace Science & Industry Corporation 731 Hospital, with permission number 2022-0204-01. Written informed consent will be obtained from the enrolled patients. Trial results will be disseminated in peer-reviewed publications.Trial registration numberChiCTR2200061453.

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