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Recruiting Not applicable

The Synergistic Effects of Integrated Neuromuscular Inhibition Technique and Dry Cupping Therapy on Pain Modulation and Functional Recovery on Myofascial Trigger Points of Upper Trapezius

NCT07027644 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-06-20
Last updated
2025-08-07

Condition(s) studied

Mechanical Neck Pain

Investigational drug(s) / intervention(s)

Dry Cupping TherapyIntegrated Neuromuscular Inhibition Techniquestretching and strengthening exercisescombined integrated neuromuscular inhibition, dry cupping and stretching and strengthening exercises

Dry Cupping Therapy: The patients receive dry cupping therapy for 10 min on the marked trigger point using a plastic set with a hand vacuum pump

Integrated Neuromuscular Inhibition Technique: The patients receive the Integrated Neuromuscular Inhibition Technique, which consists of ischemic compression, strain-counterstrain, and muscle energy techniques.

stretching and strengthening exercises: The patients receive stretching and strengthening exercises

combined integrated neuromuscular inhibition, dry cupping and stretching and strengthening exercises: the patients recive all the three interventions

Study summary

The purpose of the study is to investigate the Synergistic Effects of the Integrated Neuromuscular Inhibition Technique and Dry Cupping Therapy on Pain Modulation and functional recovery on Myofascial Trigger Points of the upper trapezius

Eligibility

Sex
ALL
Min age
18 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: * Medically competent men and women will be included They had chronic MTrPs in the upper trapezius for more than 6 months Diagnostic criteria of being a tight band with a palpable nodule and distant pain when subjected to pressure Exclusion Criteria: * subjects with previous neck or shoulder pathology (e.g., fracture, sur¬gery, inflammatory and infectious diseases), cervical disc pathology, systemic disorder, fibromyalgia, those who underwent physical therapy for at least the previous 3 months

Primary outcome measure(s)

  • Pain intensity — 0-4 weeks
    pain intensity will be measured by visual analogue scale
  • pain pressure threshold — 0-4 weeks
    The pressure algometer will measure the pain pressure threshold

Trial sites (1)

FacilityCityRegionStatus
Faculty of Physical Therapy Giza Egypt Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07027644 on ClinicalTrials.gov ↗ ← All trials in Egypt