Journal
MUSCULOSKELETAL SCIENCE AND PRACTICE
Volume 56, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.msksp.2021.102456
Keywords
Myotonometry; Tensiomyography; Upper trapezius; Trigger points; Pain
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DN treatment for UT LTrP can decrease muscle dynamic stiffness, tone, and contraction time, while increasing maximal radial displacement of the muscle belly. Additionally, pressure pain perception decreases after needling.
Background: Latent trigger point (LTrP) can cause motor dysfunction and disturb normal patterns of motor recruitment. Objective: To analyze the effects of DN in the upper trapezius (UT) LTrP on pain and the mechanical and contractile properties of the muscle. Design: A randomized, double-blinded, parallel-group-trial. Methods: Fifty healthy volunteers with LTrPs in the UT were randomly divided into a DN-group (n = 26) and a Sham-DN-group (n = 24) and received one session of DN or placebo treatment. Mechanical and contractile properties of the muscle and pressure pain perception (PPP) were evaluated before treatment and in a 30min, 24 h and 72 h follow-up after treatment. Results: In the mechanical properties, the DN-group showed lower values than the Sham-DN-group for dynamic stiffness at 72 h (p = 0.04). The DN-group showed lower values for dynamic stiffness at 72 h from baseline (278.74 +/- 38.40 to 261.54 +/- 33.64 N/m; p = 0.01) and for tone at 72 h from 30min (16.62 +/- 1.27 to 15.88 +/- 1.31 Hz; p = 0.01). In the contractile properties, the DN-group showed higher values for maximal radial displacement (Dm) of the muscle belly at 72 h from baseline (5.38 +/- 1.67 to 6.13 +/- 1.70 mm; p = 0.04), higher values for contraction time at 30min (28.53 +/- 8.80 s; p = 0.03) and lower ones at 72 h (24.74 +/- 4.36 s; p = 0.04) from baseline (26.97 +/- 6.63 s). The DN-group showed a decrease of PPP from baseline to 72 h after treatment (5.16 +/- 1.33 to 4.02 +/- 0.97 mm; p < 0.01). Conclusion: The application of DN in healthy volunteers over LTrPs in the UT decreased dynamic stiffness, tone and contraction time and increased Dm at 72 h after treatment. Additionally, the PPP showed a decrease at 72 h after needling. ClinicalTrials.gov: NCT04466813
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