The purpose of this clinical trial is to compare the effects of deep versus superficial dry needling (DN) on the ultrasound and electromyographic (EMG) characteristics of myofascial trigger points (MTrPs) in the upper trapezius muscle of patients with neck pain. Researchers aim to determine which dry needling technique produces greater improvements in muscle properties (ultrasound and EMG findings), pain intensity, and functional disability. Intervention: Participants will be randomly assigned to receive either deep DN or superficial DN. Each participant will undergo four treatment sessions over a two-week period. Assessments: Outcomes will be measured at three time points: * Baseline (before treatment) * Post-treatment (end of week 2) * Follow-up (4 weeks after treatment)
Age range
18 Years – 65 Years
Sex
ALL
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Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Upper Trapezius Muscle Thickness by B-mode Sonography
Timeframe: Baseline, Post two weeks and post 4 weeks
Upper Trapezius Muscle Stiffness by Strain Elastography
Timeframe: Baseline, Post two weeks and post 4 weeks
Blood Flow by Doppler ultrasonography
Timeframe: Baseline, Post two weeks and post 4 weeks
Upper Trapezius Muscle Activity and Fatigability by Surface Electromyography
Timeframe: Baseline, Post two weeks and post 4 weeks