- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07574112
Muscle Energy Technique With And Without Myofascial Release in Patients With Cervicogenic Headache
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This randomized controlled trial was conducted to compare the effects of Muscle Energy Technique (MET) with and without Myofascial Release (MFR) in patients with cervicogenic headache. Cervicogenic headache is a secondary headache arising from dysfunctions of the cervical spine and associated muscular structures.
A total of 40 participants aged between 20 and 40 years were recruited and randomly allocated into two equal groups. Group A received Muscle Energy Technique alone, while Group B received a combination of Muscle Energy Technique and Myofascial Release. The intervention was delivered over five treatment sessions within a period of two weeks.
Outcome measures included pain intensity assessed using the Visual Analogue Scale (VAS), cervical range of motion measured with a goniometer, and functional disability assessed using the Neck Disability Index (NDI). Assessments were performed at baseline and after completion of the intervention period.
The objective of the study was to determine whether the addition of Myofascial Release to Muscle Energy Technique provides superior improvements in pain reduction, cervical mobility, and functional disability compared to Muscle Energy Technique alone in patients with cervicogenic headache.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab Province
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Lahore, Punjab Province, Pakistan
- University of Lahore
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Participants aged 20 to 40 years
- Diagnosed with cervicogenic headache
- Both male and female participants
- Participants willing to participate in the study
Exclusion Criteria:
- History of cervical fracture or surgery
- Neurological disorders affecting the cervical region
- Severe cervical spine pathology
- Participants receiving other forms of manual therapy
Study Plan
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 |
|---|---|
|
Active Comparator: Muscle Energy Technique (MET)
Participants in this group received Muscle Energy Technique (MET) alone.
The intervention was applied over five treatment sessions within two weeks.
This group served as the comparison group to evaluate the effects of MET without Myofascial Release.
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Muscle Energy Technique (MET) was applied to the cervical region muscles using isometric contractions followed by passive stretching.
The technique was performed in a controlled manner to improve muscle flexibility, reduce pain, and enhance cervical mobility over five treatment sessions within two weeks.
Other Names:
|
|
Experimental: Muscle Energy Technique (MET) + Myofascial Release (MFR)
Participants in this group received a combination of Muscle Energy Technique (MET) and Myofascial Release (MFR).
The intervention was delivered over five treatment sessions within two weeks to evaluate its combined effect on pain, cervical range of motion, and disability.
|
Muscle Energy Technique (MET) was applied to the cervical region muscles using isometric contractions followed by passive stretching.
The technique was performed in a controlled manner to improve muscle flexibility, reduce pain, and enhance cervical mobility over five treatment sessions within two weeks.
Other Names:
Sustained manual pressure applied to cervical and upper trapezius muscles to release fascial restrictions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Intensity (Viscual Analogue Scale)
Time Frame: Baseline and 2 weeks post-intervention
|
Pain intensity was assessed using the Visual Analogue Scale (VAS).
The scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates worst possible pain.
Higher scores indicate greater pain intensity.
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Baseline and 2 weeks post-intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cervical Range of Motion
Time Frame: Baseline and 2 weeks post-intervention
|
Cervical range of motion was assessed using a goniometer to measure flexion, extension, lateral flexion, and rotation of the cervical spine.
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Baseline and 2 weeks post-intervention
|
|
Neck Disability Measured by Neck Disability Index (NDI)
Time Frame: Baseline and 2 weeks post-intervention
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Functional disability was assessed using the Neck Disability Index (NDI).
The scale ranges from 0 to 50, where higher scores indicate greater disability related to neck pain.
|
Baseline and 2 weeks post-intervention
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Samreen Z, Waseem I, Mustansar A. Muscle Energy Technique With and Without Myofascial Release in Patients with Cervicogenic Headache. Insights in Journal of Health Research. 2025. https://doi.org/10.71000/vy8k2r11
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Headache Disorders
- Headache Disorders, Secondary
- Post-Traumatic Headache
- Therapeutics
- Complementary Therapies
- Physical Therapy Modalities
- Rehabilitation
- Therapy, Soft Tissue
- Musculoskeletal Manipulations
- Massage
- Myofascial Release Therapy
Other Study ID Numbers
- MS-UOL-2024-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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