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Clinical Trials/NCT04394741
NCT04394741
Completed
Not Applicable

Effects of Dry Needling on Stiffness in Latent Myofascial Trigger Points: a Randomized Controlled Trial

University of Castilla-La Mancha1 site in 1 country51 target enrollmentJune 1, 2020
ConditionsTrigger Points

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Trigger Points
Sponsor
University of Castilla-La Mancha
Enrollment
51
Locations
1
Primary Endpoint
Change on Stiffness (Shear wave elastography and Strain Elastography)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to determine whether application of Dry Needling (DN) is effective for reduced on Stiffness in Latent trigger point (LTrP) of upper trapezius. The secondary purposes are to determine the correlation on two elastography for stiffness measure (Shear-wave elastography and Strain elastography). Randomized controlled trial, in parallel with cross-control design. Two groups with LTrP in upper trapezius, and will be randomly selected to DN group or Sham-Dn group.

Registry
clinicaltrials.gov
Start Date
June 1, 2020
End Date
August 31, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Castilla-La Mancha
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age between 18 and 30 years
  • The presence of LTrP in the middle third of the upper trapezius muscle on the dominant side
  • Being able to provide written informed consent
  • Being able to follow instructions and realize clinical tests

Exclusion Criteria

  • Any pharmacological therapeutic
  • Any medical treatment or physical therapies at cervical region during the 6-month before this study - Any diagnosed health problem
  • Any history of head and upper extremity surgery or trauma
  • Any red flags to DN, (ie: metabolic diseases, pregnancy, kinesiophobia, Infection, cancer)
  • Absence of recurrent history of neck pain
  • No neck pain symptomatology the previous 6 months
  • Cervical disk herniation

Outcomes

Primary Outcomes

Change on Stiffness (Shear wave elastography and Strain Elastography)

Time Frame: Baseline, at 30 minutes after treatment, at 24 hours after treatment, at 72 hours after treatment

Shear-wave Elastography (SWE) as assessed using an Logiq S8 US system (GE Healthcare). The stiffness was determined with measuring velocity of shear waves in trapezius muscle on SWE exam. Strain elastography (SEL) as assessed using an Logiq S8 US system (GE Healthcare). The stiffness was determined by applying light repetitive compression with the hand-held transducer

Secondary Outcomes

  • Change in Thickness of muscle(Baseline, at 30 minutes after treatment, at 24 hours after treatment, at 72 hours after treatment)
  • Change in Post-needling soreness(Baseline, at 30 minutes after treatment, at 24 hours after treatment, at 72 hours after treatment)
  • Change in Pain Pressure Threshold (PPT)(Baseline, at 30 minutes after treatment, at 24 hours after treatment, at 72 hours after treatment)

Study Sites (1)

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