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Effects of manual and instrumental therapy on the treatment of myofascial pain syndrome in descending trapezius of women: a blind randomized clinical study |
Florianovicz VC, Bueno BS, Dalpiaz A, Kuriki HU, Marcolino AM, Diefenthaeler F, de Oliveira Guirro EC, Barbosa RI |
Muscles, Ligaments and Tendons Journal 2024 Jan-Mar;14(1):75-86 |
clinical trial |
9/10 [Eligibility criteria: Yes; Random allocation: Yes; Concealed allocation: Yes; Baseline comparability: Yes; Blind subjects: Yes; Blind therapists: No; Blind assessors: Yes; Adequate follow-up: Yes; Intention-to-treat analysis: Yes; Between-group comparisons: Yes; Point estimates and variability: Yes. Note: Eligibility criteria item does not contribute to total score] *This score has been confirmed* |
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.
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