Comparing Between Mulligan Technique and Active Release Technique in Treatment of Chronic Mechanical Neck Pain
MWM/ART
Effect of Mulligan Mobilization Technique Versus Active Release Technique on Chronic Non-specific Neck Pain
1 other identifier
interventional
36
0 countries
N/A
Brief Summary
This study will be conducted to compare between Mulligan mobilization technique and Active release technique in management of non-specific chronic neck pain as regard to neck pain, cervical range of motion and neck function.
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 Jul 2026
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
June 25, 2026
CompletedFirst Posted
Study publicly available on registry
July 1, 2026
CompletedStudy Start
First participant enrolled
July 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
CompletedJuly 1, 2026
June 1, 2026
1 month
June 25, 2026
June 25, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Cervical range of motion
Cervical ROM will be assessed using CROM device.
4 weeks
Secondary Outcomes (2)
Neck function
4 weeks
Pain intensity
4 weeks
Study Arms (3)
conventional treatment
ACTIVE COMPARATORThis group will receive only the conventional treatment 3 sessions per week for four weeks
Mulligan mobilization technique
EXPERIMENTALtwelve participants will receive mulligan mobilization for cervical spine: Participant will sit comfortably supported in a chair with a neutral head and cervical spine position
active release technique
EXPERIMENTALtwelve participants will receive active release technique for cervical spine The patient will sit on a stool with hands supported on the thighs, the therapist will apply deep pressure on both sides of levator scapulae and upper trapezius muscles (over the area of tenderness) and the patient will be instructed to actively move the muscle from a shortened to lengthened position and thereby breaking adhesions.1 set of 3-5 repetitions in one session
Interventions
twelve participants will receive only the conventional physical therapy program prescribed for chronic non-specific neck pain in the form of: 1.Source of superficial heat using hot packs for 15 minutes. 2.Postural correction exercises. 3.Isometric strengthening exercises for neck muscles in all directions (Flexion, extension, side bending and rotation). 4.Stretching for common tight muscles (Trapezius, levator scapulae and sternocleidomastoid muscles). 5.Chin tuck exercises. 6.Scapular stabilization exercises
Participant will sit comfortably supported in a chair with a neutral head and cervical spine position. Practitioner, A gentle, painless posterior-to-anterior (PA) glide will be applied to the facets (bony projections) on the spinous process or the articular pillar/cervical lamina. This glide will be maintained throughout the movement. Participant Action: While the glide will be held, the participant actively will move their neck in the direction that previously caused pain. If pain-free, the participant can gently push further into the movement restriction
The patient will sit on a stool with hands supported on the thighs, the therapist will apply deep pressure on both sides of levator scapulae and upper trapezius muscles (over the area of tenderness) and the patient will be instructed to actively move the muscle from a shortened to lengthened position and thereby breaking adhesions.1 set of 3-5 repetitions in one session
Eligibility Criteria
You may qualify if:
- The participants will be included in this study if they meet the following criteria:
- Have referred from orthopedic surgeon diagnosed with NSCNP that has been localized to the cervical and periscapular areas for at least three months
- Aged from 18-40 years
- Having a score more than 10 on the Neck disability index (NDI)
- BMI from 18.5 to 29.9 kg/m2.
You may not qualify if:
- The Participants will be excluded from this study if they meet any of the following criteria
- History of previous neck surgery.
- Recent or old fractures.
- Cognitive impairment and inability to understand the scale.
- Systematic inflammatory disease e.g., rheumatoid arthritis and ankylosing spondylitis, neck pain with radiculopathy or neuropathy.
- A score of below 10 or above 40 points out of 50 on the NDI.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
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
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Lecturer
Study Record Dates
First Submitted
June 25, 2026
First Posted
July 1, 2026
Study Start
July 1, 2026
Primary Completion
August 1, 2026
Study Completion
August 1, 2026
Last Updated
July 1, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share