Effects of Manual and Instrumental Therapy on the Treatment of Myofascial Pain Syndrome in Descending Trapezius of Women: A Blind Randomized Clinical Study

R. Barbosa, Vivian Carla Florianovicz, Bruna Scheffer Bueno, Ameg Dalpiaz, H. Kuriki, A. Marcolino, Fernando Diefenthaeler, E. C. D. O. Guirro
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Abstract

Objective. To investigate the effects of Manual Ischemic Compression (MIC) and Instrumental Ischemic Compression (ICG) and Pressure Algometer (ICA), in the treatment of women with MPS in descending trapezius. Patients and Methods. This is a double-blinded, randomized, placebo-controlled trial. Patients were randomized into 3 groups: MIC, ICG, and ICA. Pain, pressure pain threshold (PPT), electromyography, disability (NDI), anxiety (GAD-7), and adverse treatment effects (AE) were assessed. The Shapiro-Wilk test was performed to verify the normality of the data, followed by consistent tests, being considered significant when p < 0.05. Results. There was no intergroup difference for any analyzed variables. In the intra-group comparison, MIC group presented pain reduction (F: 7.70; p = 0.0002), between baseline and 1 week; and anxiety (p = 0.048), between baseline and 4 weeks. All groups showed increase in PPT (F: 37.62; p < 0.0001) and decrease in NDI score (F: 53.29; p < 0.0001). About AE, the MIC group reported the highest mean value of discomfort after the technique, 7.22. Conclusions. An intragroup improvement was observed in the pain and anxiety variables for the MIC group, when compared to the baseline with one week and four weeks, respectively. There was an improvement in all groups in the PPT and NDI; however, with no differences between groups in the post-treatment. Study registration. Brazilian Registry of Clinical Trials: ReBEC: RBR-2q24nb.
手法和器械疗法对治疗女性下斜方肌肌筋膜疼痛综合征的效果:盲法随机临床研究
目的研究手动缺血加压(MIC)和器械缺血加压(ICG)及压力计(ICA)在治疗斜方肌下段 MPS 女性患者中的效果。患者和方法。这是一项双盲、随机、安慰剂对照试验。患者被随机分为 3 组:MIC、ICG 和 ICA 组。对疼痛、压痛阈值(PPT)、肌电图、残疾(NDI)、焦虑(GAD-7)和治疗不良反应(AE)进行评估。为验证数据的正态性,进行了 Shapiro-Wilk 检验,然后进行了一致性检验,当 P < 0.05 时,认为数据具有显著性。结果所有分析变量均无组间差异。在组内比较中,MIC 组在基线和 1 周之间疼痛减轻(F:7.70;P = 0.0002);在基线和 4 周之间焦虑减轻(P = 0.048)。所有组的 PPT 均有增加(F:37.62;p < 0.0001),NDI 评分均有下降(F:53.29;p < 0.0001)。关于 AE,MIC 组报告的术后不适感平均值最高,为 7.22。结论与一周和四周的基线相比,MIC 组的疼痛和焦虑变量在组内均有改善。各组的 PPT 和 NDI 均有所改善,但治疗后组间无差异。研究注册。巴西临床试验登记处:ReBEC:RBR-2q24nb。
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