CompletedNot Applicable

Effects of Dry Needling on Stiffness in Latent Trigger Points

Spain51 participantsStarted 2020-06-01

Plain-language 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.

Who can participate

Age range18 Years – 30 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Change on Stiffness (Shear wave elastography and Strain Elastography)

Timeframe: Baseline, at 30 minutes after treatment, at 24 hours after treatment, at 72 hours after treatment

Trial details

NCT IDNCT04394741

SponsorUniversity of Castilla-La Mancha

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2020-07-31

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