CompletedNot Applicable

Effect of Dry Needling on Surface Electromyographic Activity in Latent Trigger Points

Spain46 participantsStarted 2021-01-04

Plain-language summary

Brief summary: The purpose of this study is to determine the effect of Dry Needling (DN) on electromyographic activity in different situations at the latent trigger point (LTrP) point of the upper trapezius. Randomized controlled trial, in parallel with the crossover control design. Two groups with LTrP in the upper trapezius, and the DN group or the Sham-Dn group will be randomly selected.

Who can participate

Age range18 Years – 30 Years

SexALL

See this in plain English?

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 onthe 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

Changes in resting surface EMG activity (amplitude, RMS)

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

Trial details

NCT IDNCT04684784

SponsorUniversity of Castilla-La Mancha

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-02-04

View on ClinicalTrials.gov More Trigger Point Pain, Myofascial trials