Positional Release Therapy vs. Dry Needling for Levator Scapulae Syndrome

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study randomizes participants with Levator Scapulae syndrome to receive either Positional Release Therapy on the levator scapulae or dry needling with neck strengthening exercises. The trial uses 1:1 randomization with a blinded outcome assessor, though patients and clinicians know the treatment due to the nature of the therapies. Outcomes are measured at baseline and after four weeks, including pain (VAS), range of motion (CROM), neck strength (Oxford Scale), disability (NDI), general health (EQ-5D), and global progress. Primary goals are to see which approach better improves pain, function, and quality of life in office- or manual-work settings. Safety monitoring and adherence will be tracked throughout the study.

Why it matters

Who can join: the full rules

Inclusion Criteria:

18-40 years Willing to participate Having Positive Levator scapulae Test -

Exclusion Criteria:

Any history related to spinal surgery, Previous administration of epidural injections. Neck pain due to specific pathology, Neurological deficits (Myelopathy) and Clinical disorder contraindicated to exercise

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Where it's running

• Sind Institute of Physical Medicine & Rehabilitation
  Karachi, Sindh, Pakistan Recruiting

Study contacts

• Study coordinator: Iram Iqbal Shamsi, MPhil
• Email: iramiqbalshamsi@gmail.com
• Phone: +92 3012135230

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.