- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05258201
Effect of Muscle Energy Technique Versus Strain-counterstrain on Upper Trapezius Trigger Points
April 21, 2022 updated by: Riphah International University
Effect of Muscle Energy Technique Versus Strain-Counterstrain on Upper Trapezius Myofascial Active Trigger Points. A Randomized Control Trial
Aim of the study To determine the comparative effects of muscle energy technique and strain counter strain in upper trapezius trigger point.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
A Randomized Controlled trial will be conducted after approval of synopsis.
To enroll patients Purposive sampling technique will be used.
Patients will be selected according to the pre-defined inclusion and exclusion criteria.
The enrolled patients will be allocated into two groups, group A and group B. On Group A muscle energy technique will be applied for 30 seconds and repeat 3 to 5 times per on treatment session and Group B will be treated with strain counter strain for 20-30 seconds and repeat this process for up to five times.
Assessment will be done at baseline, 2nd week, 4th week and 6th week of treatment.
Follow up will be assessed 15 days after completion of treatment protocol.
The patients' outcome will be measured by Visual Analog Scale for pain intensity and Neck Disability Index .
Informed consent will be taken from each patient.
Statistical Package of Social Sciences software, version 20 will be used for the analysis of data.
Study Type
Interventional
Enrollment (Actual)
50
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Punjab
-
Faisalabad, Punjab, Pakistan, 38000
- Ripah International university
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 34 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Participants who are 18 to 34 years old
- In upper trapezius From 2 weeks Had mechanical neck pain and was diagnosed with active myofacial Trigger points
- Subjects have to exhibit a tendor point in the upper trapezius muscle either on the left or right side
- Local pain is greater than 3/10 on Visual Analog scale
Exclusion Criteria:
- Patient with cervical radiculopathy
- Patients with Fibromyalgia syndrome
- Patients who had cervical spine surgery
- Patient with myelopathy
- Patients who had myofacial pain therapy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Muscle Energy Technique
Muscle energy Technique will be applied on the subjects, when they will be lying supine and on the effect side therapist will stabilize shoulder by one hand, while the ear / mastoid area of the affected side will be hold by opposite hand.
The head and neck will be bend to contralateral side, then bends on the same side.
Subject will raise his shoulder with the shoulder fixed to the ear with less effort than the maximum.
Isometric contraction will be maintain for 7-10 seconds.
This position will be held for 30 seconds and repeat three to five times per on treatment session
|
Muscle Energy Technique is a common way to achieve muscle tension release (stop) before stretching other's adductor muscles
|
|
Experimental: Strain-counterstrain
Strain And Counter Strain will be applied on subject in normal position and will be produced by placing the muscle in a short / relaxed position, the point where the pain will reduce of at least 70% will be produce will easily define.
The patient will be in a supine position while the doctor will place the labial arm in flexion, abduction and external rotation to reduce the reported Trp pain.
Once the position is easy to find, the pressure will be apply to the Trp and will be hold for 20-30 seconds and repeat this process for up to five times
|
Strain-counterstrain is also used for manual Trigger Point processing.
This involves identifying active TRP and then applying pressure until a ridiculous reaction occurs.
The area is then positioned to reduce tension in the injured muscle and later reduce tripod pain.
When the pain subsides, the tissues that are most stressed feel relaxed and there is a local decrease in the ground
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analogue Scale
Time Frame: 12th Week
|
A Visual Analogue Scale is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured.
It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms.
|
12th Week
|
|
Neck Disability Index
Time Frame: 12th Week
|
The Neck Disability Index is a 10-item questionnaire that measures a patient's self-reported neck pain related disability.
A higher Neck Disability Index score means the greater a patient's perceived disability due to neck pain
|
12th Week
|
|
Goniometer
Time Frame: 12th Week
|
Goniometer has been the most widely used tool for measuring joint range of motion.
To ensure reliable measurement, standardized, specific positions and landmarks are used to measure Cervical lateral flexion range of motion.
|
12th Week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2021
Primary Completion (Actual)
March 20, 2022
Study Completion (Actual)
March 25, 2022
Study Registration Dates
First Submitted
February 20, 2022
First Submitted That Met QC Criteria
February 20, 2022
First Posted (Actual)
February 28, 2022
Study Record Updates
Last Update Posted (Actual)
April 22, 2022
Last Update Submitted That Met QC Criteria
April 21, 2022
Last Verified
April 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC-FSD-00268
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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