Can Myotonometry Quantify Dry Needling Effectiveness on Myofascial Trigger Points?

Muscle Tone Abnormalities Clinical Trial

Official title: Can Myotonometry Quantify Dry Needling Effectiveness on Myofascial Trigger Points?

Status Completed

Clinical Trial Summary

The main objective of this study is to assess effects of Dry Needling into Myofascial Trigger Point compared Dry Needling into Taut Band point based on the outcomes of myotnometric measurement in healthy subjects. Hypothesis: Deep Dry Needling of the latent medial Myofascial Trigger Point (MTrP) of the soleus muscle will achieve changes in myotonometric measures compared to Deep Dry Needling of the Taut Band of the soleus muscle.

Clinical Trial Description

Methods: It is a double-blinded randomized clinical trial where subjects are healthy volunteers from the city of Toledo older than 18 years. There will be a MTrP Group (dry needling into the medial MTrP of soleus muscle) and a TB Group (dry needling distal to the MTrP but into the taut muscle band of soleus muscle). The intervention will be a unique session. Intervention: Dry needling technique will be performed by locating the taut band and the Myofascial Trigger Point. Depending on the group, a thin needle (0,32x40mm) is introduced 10 times (fast in and fast out) directly within the Myofascial Trigger Point or within the Taut Band. Assessment: Myoton device is a simple and portable tool to obtain quantitative and objective assessments of mechanical properties of muscle tone. Myoton has been adopted to characterize the viscoelastic properties of skeletal muscle as tissue displacement when a mechanical perturbation is applied to the muscle. The device incorporates a probe and an acceleration sensor. The probe was kept perpendicular with its end touching the muscle belly. 10 mechanical impacts (with a duration of 15 ms, a force of 0.4 N and a local deformation in the order of a few millimetres) are delivered to MTrP and TB points. Outcome measures: Outcome measures will include myotonometric measurements (frecuency, stiffness and decrement) and they will be evaluated before, at 10 min and 1 week after the intervention. ;

Related Conditions & MeSH terms

• Congenital Abnormalities
• Muscle Tone Abnormalities

• NCT number: NCT02952053
• Study type: Interventional
• Source: University of Castilla-La Mancha
• Status: Completed
• Phase: N/A
• Start date: December 12, 2015
• Completion date: July 31, 2017