Myofascial Release With and Without Autogenic Inhibition Muscle Energy Technique in Non-specific Chronic Neck Pain
Effects of Myofascial Release With and Without Autogenic Inhibition Muscle Energy Technique in Patients With Non-specific Chronic Neck Pain
1 other identifier
interventional
44
1 country
1
Brief Summary
The study was conducted to determine the effects of myofascial release therapy with and without autogenic inhibition muscle energy technique in patients with non-specific chronic neck pain.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 13, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 31, 2025
CompletedFirst Submitted
Initial submission to the registry
December 29, 2025
CompletedFirst Posted
Study publicly available on registry
January 12, 2026
CompletedJanuary 12, 2026
December 1, 2025
5 months
December 29, 2025
December 29, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Numeric Pain Rating Scale
Numeric Pain Rating Scale is utilized to evaluate pain. It consists of 11 points, having an overall score ranging from 0 and 10, where: 0 represents no pain, 1 - 3 represents mild pain, 4 - 6 represents moderate pain and 7 - 10 represents the most severe pain.
From enrollment to the end of treatment at 6 weeks
Neck Disability Index
Neck Disability Index is a questionnaire that has 10-questions for determining cervical pain and functional disability linked with the activities of daily living. It consists of questions on pain intensity, personal care, lifting, reading, headaches, concentration, work, driving, sleeping and recreation. Scores in each item is described in 6 stages, from 0 to 5 points. The total of 0-4 points indicate no disability, 5-14 points indicate mild disability, 15-24 points indicate moderate disability, 25-34 points indicate severe disability and 35-50 points indicate complete disability
From enrollment to the end of treatment at 6 weeks
Secondary Outcomes (6)
ROM Cervical Spine (Flexion)
From enrollment to the end of treatment at 6 weeks
ROM Cervical Spine (Extension)
From enrollment to the end of treatment at 6 weeks
ROM Cervical Spine (Lateral Flexion) Left Side
From enrollment to the end of treatment at 6 weeks
ROM Cervical Spine (Lateral Flexion) Right Side
From enrollment to the end of treatment at 6 weeks
ROM Cervical Spine (Rotation) Left Side
From enrollment to the end of treatment at 6 weeks
- +1 more secondary outcomes
Study Arms (2)
Myofascial Release with Autogenic Inhibition Muscle Energy Technique
EXPERIMENTALMyofascial Release Therapy
ACTIVE COMPARATORInterventions
AI MET was applied for upper trapezius 5 times for each side, similarly for levator scapulae it was applied 5 times for each side. AI MET was applied for posterior, middle and anterior fibres of scalene muscle. For sternocleidomastoid muscle it was applied for at least twice for each side. 8 sessions were conducted for 6 weeks, with 3 sessions scheduled every week.
MFR for upper trapezius and levator scapulae was carried out 5 times for each side. A total of 18 sessions were conducted for 6 weeks, with 3 sessions scheduled every week.
Electric hot pack for 10 minutes for 10 minutes, TENS with frequency of 120Hz at low intensity having pulse duration of 50-200μs for 10 minutes \& Grade I and II Maitland posteroanterior central glide with 3 sets of 30 oscillations, for alleviation of pain at the target vertebral segment.
Eligibility Criteria
You may qualify if:
- Neck pain for at least 3 months
- Pain intensity on NPRS between 4 to 7
- Limited neck range of motion
- Use of computer for at least 2 hours daily
- Negative Sharp-Purser and alar ligaments test (to rule out atlantoaxial instability, integrity of transverse and alar ligaments)
You may not qualify if:
- History of trauma
- Cervical spine fracture
- Open neck surgery
- Cervical radiculopathy
- Paresthesia
- Cervical myelopathy
- Rheumatoid Arthritis
- Ankylosing Spondylitis
- Multiple Sclerosis
- Fibromyalgia
- Hemorrhage tendency and/or anticoagulation treatment
- Whiplash Injury
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Rehab Max Physio & Sports Injury Clinic
Layyah, Punjab Province, 31200, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Shakil ur Rehman, Ph.D
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 29, 2025
First Posted
January 12, 2026
Study Start
January 13, 2025
Primary Completion
May 31, 2025
Study Completion
October 31, 2025
Last Updated
January 12, 2026
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share