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Clinical Trials/NCT05614830
NCT05614830
Not yet recruiting
Not Applicable

Effectiveness of Dry Needling in Management of Myofacial Trigger Point In Trapezius Muscle

Taif University0 sites40 target enrollmentJanuary 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myofacial Trigger Points
Sponsor
Taif University
Enrollment
40
Primary Endpoint
Pain level
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

myofascial pain syndrome is considered to be a chronic condition due to sensitive pressure points within the muscle recognized as trigger points

Generally the aim of this study will be :

  • To investigate the effectiveness of dry needling on trigger point in trapezius muscle
  • Evaluate the pain level before and after the applications of dry needling on trigger points
  • compare between the effects of dry needling and physical therapy exercise program
Registry
clinicaltrials.gov
Start Date
January 2023
End Date
June 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Slwa Sami Alattar

Student

Taif University

Eligibility Criteria

Inclusion Criteria

  • Clinically active trigger point and expression of symptoms of neck pain in trapezius which had lasted for at least 3 months.
  • Having a pain level higher than 4 and lower than 8 on Visual Analogue Scale ( VAS )
  • Did not receive any other form of neck treatment during the previous month.

Exclusion Criteria

  • Presence of cardiopulmonary disease , the application process requires the subject to be in prone position to expose the area of treatment, this position is un-preferable for cardiopulmonary patients
  • History of neck surgery
  • Trigger point treatment in the last 30 days
  • Any contraindications for dry needling such as local infection, skin disease ,severe postural disorder , tumor , rheumatoid arthritis, cervical spine stenosis and bilateral upper extremity symptoms
  • pregnancy

Outcomes

Primary Outcomes

Pain level

Time Frame: 6 weeks

Will be determined using the visuals analogue scale (VAS)

Neck disability index

Time Frame: 6 weeks

questionnaire contains 10 items aiming to evaluate the limitation because of neck pain

Secondary Outcomes

  • Depression(6 weeks)
  • Neck Range of motion(6 weeks)

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