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Clinical Trials/NCT04285216
NCT04285216
Completed
N/A

Combined Effects of Dry Needling and Strain Counter Strain Technique in Myofascial Trigger Points of Upper Trapezius

Riphah International University1 site in 1 country28 target enrollmentSeptember 15, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Trigger Point Pain, Myofascial
Sponsor
Riphah International University
Enrollment
28
Locations
1
Primary Endpoint
Numeric Pain Rating Scale (NPRS)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

To determine the effects of Dry Needling and Strain Counter Strain Technique in Myofascial Trigger Points of Upper Trapezius

Detailed Description

It is Randomized Controlled trail will be conduct in Mayo Hospital Lahore and Alnoor Hospital Awan town Lahore. Non probability consecutive sampling technique will be used to collect the data. Each group contain the 14 patients, Patient will be divided into two groups. Group A will be experimental group treated by Dry needling and strain counter strain with baseline treatment and Group B will be control group treated by Strain counter strain with baseline treatment(Hot pack 10 mints,stretching,Neck isometrics). Neck Disability index (NDI) ,visual analogue scale(VAS) and goniometer will be used as data collecting tools.

Registry
clinicaltrials.gov
Start Date
September 15, 2019
End Date
August 28, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with non-specific neck pain, having active myofascial trigger points in upper trapezius muscle.
  • Patient of both gender under the age of 20-40 year
  • bilateral pain involving the upper trapezius
  • a duration of pain of at least 3 months
  • pain localized in the cervical and occipital regions but not in the orofacial region.
  • restricted cervical range of motion(side flexion)

Exclusion Criteria

  • history of traumatic injuries (e.g., contusion, fracture, and whiplash injury)
  • needle phobia patients.
  • systemic diseases such as blood coagula tion disorders, chronic pain syndrome, cancer,allergies fibromyalgia, systemic lupus erythematous, and psoriatic arthritis.
  • cervical spine surgery patients.
  • orofacial pain and temporomandibular disorders
  • neurologic disorders (e.g., trigeminal neuralgia or occipital neuralgia)
  • medical diagnosis of any primary headache (tension type or migraine) clinical diagnosis of cervical radiculopathy or myelopathy
  • history of previous physical therapy intervention for the cervical region in last 6 month
  • use of anticoagulants, opioids or antiepileptic medications

Outcomes

Primary Outcomes

Numeric Pain Rating Scale (NPRS)

Time Frame: 4 months

The Numerical Pain Rating Scale (NPRS) is a subjective measure in which individuals rate their pain on an eleven-point numerical scale. The scale is composed of 0 (no pain at all) to 10 (worst imaginable pain).

Range of Motion

Time Frame: 4 months

Standard Goniometer will be used.Higher score shows improvement.

Secondary Outcomes

  • Disability(4 months)

Study Sites (1)

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