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

Sponsor
Riphah International University (Other)
Overall Status
Completed
CT.gov ID
NCT04285216
Collaborator
(none)
28
1
2
11.4
2.4

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Other: Dry Needling
  • Other: Strain counter strain
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
28 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
Outcome Assessor will be binded
Primary Purpose:
Treatment
Official Title:
Combined Effects of Dry Needling and Strain Counter Strain Technique in Myofascial Trigger Points of Upper Trapezius
Actual Study Start Date :
Sep 15, 2019
Actual Primary Completion Date :
Jun 20, 2020
Actual Study Completion Date :
Aug 28, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Dry needling

Hot pack 10 mints,stretching,Neck isometrics, dry needling(DN) and Strain counterstrain(SCS)

Other: Dry Needling
Hot pack 10 mints,stretching,Neck isometrics, dry needling(DN) and Strain counterstrain(SCS)

Active Comparator: Strain counter strain

Hot pack 10 minutes, stretching,Neck isometrics, Strain counter strain (S C S)

Other: Strain counter strain
Hot pack 10 mints, stretchings,Neck isometrics, Strain counterstrain(SCS)

Outcome Measures

Primary Outcome Measures

  1. Numeric Pain Rating Scale (NPRS) [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).

  2. Range of Motion [4 months]

    Standard Goniometer will be used.Higher score shows improvement.

Secondary Outcome Measures

  1. Disability [4 months]

    Scoring: For each section the total possible score is 5: if the first statement is marked the section score = 0, if the last statement is marked it = 5. If all ten sections are completed the score is calculated as follows: Example:16 (total scored) 50 (total possible score) x 100 = 32% If one section is missed or not applicable the score is calculated: 16 (total scored) 45 (total possible score) x 100 = 35.5% Minimum Detectable Change (90% confidence): 5 points or 10 %points

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Hospital Lahore Pakistan 54000

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: Maryam Shabbir, Phd, Riphah International University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT04285216
Other Study ID Numbers:
  • MSOMPT/Spring19/031 Aqsa Aroob
First Posted:
Feb 26, 2020
Last Update Posted:
Sep 22, 2020
Last Verified:
Sep 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Riphah International University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 22, 2020