Comparing dry needling techniques for upper trapezius muscle pain
Treatment of Upper Trapezius Muscle Myofascial Pain Syndrome: Comparison of Ultrasound- Guided Dry Needling Techniques
This study is testing two different dry needling methods to see which one helps people aged 20 to 50 with upper trapezius muscle pain feel better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 20 Years to 50 Years |
| Sex | All |
| Sponsor | Abant Izzet Baysal University Academic / other |
| Locations | 1 site (Bolu) |
| Trial ID | NCT06546124 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of two dry needling techniques—superficial and deep—guided by ultrasound in treating myofascial pain syndrome of the upper trapezius muscle. Participants will be assessed for pain, disability, functional impairment, and quality of life following treatment. The use of ultrasound is intended to enhance the precision of needle placement, potentially improving treatment outcomes. The study will include patients aged 20 to 50 who have not received any cervical treatments in the past three months.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 20 to 50 diagnosed with myofascial pain syndrome in the upper trapezius muscle.
Not a fit: Patients with a history of neck and shoulder trauma or other conditions affecting neck and shoulder pain may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a more effective treatment option for patients suffering from myofascial pain syndrome.
How similar studies have performed: Previous studies have shown promising results with dry needling techniques, but this specific comparison using ultrasound guidance is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Diagnosis of MPS in the upper trapezius muscle in accordance with criteria defined by Travell and Simons 2. Ages between 20 and 50 years 3. No treatment, including injections, dry needling, and physical methods, applied to the cervical region in the last three months Exclusion Criteria: 1. Bleeding Tendency 2. History of Neck and Shoulder Trauma 3. Other Conditions Affecting Neck and Shoulder Pain: including malignancy, infection, rheumatic diseases, degenerative joint disease, fibromyalgia, cervical radiculopathy, neuropathy, myelopathy, myopathy, adhesive capsulitis, etc. 4. Cases Where Evaluation Could Not Be Completed for Any Reason 5. Patients Who Refuse to Complete the Evaluations
Where this trial is running
Bolu
- Abant Izzet Baysal University — Bolu, Turkey (Recruiting)
Study contacts
- Study coordinator: Serdar Kılınç
- Email: drserdarkilinc@hotmail.com
- Phone: 905055913181
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.