Mckenzie Versus Maitland Cervical Mobilization Technique in Management of Non-specific Neck Pain.

December 5, 2025 updated by: Mahmoud Salah Abd-Elfattah, Cairo University
This study will be conducted to compare between Mckenzie exercises and Maitland cervical mobilization technique in management of non-specific neck pain as regard to neck pain, cervical range of motion, neck function and cervical proprioception.

Study Overview

Detailed Description

Neck pain is the second leading cause of disability worldwide among people with musculoskeletal disorders , and neck pain is responsible for a substantial burden to society .

Current guidelines advocate a multimodal approach including different types of exercise and manual therapy for managing non-specific neck pain and there is little evidence of what specific intervention of this multimodal approach is most beneficial. This means that there is a gap in literature regarding this point in general. If effectiveness of each intervention is clear, this will inform selection of individual components of the multimodal approach.

45 Subjects of both genders with a primary complaint of neck pain more than 12 weeks will participate in this study.Group A will receive Mckenzie exercise in the form of repeated movements in the direction of painful & restricted movement .Group B: will receive Maitland's cervical mobilization in the form of posterior-anterior (PA) glide.Group C: will receive only the conventional physical therapy program prescribed in the form of ( hot packs , stretching exercises, isometric strengthening exercises and postural correction exercises).

Study Type

Interventional

Enrollment (Estimated)

45

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 Contact

Study Contact Backup

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

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion criteria:

  • 45 Subjects diagnosed and referred from orthopedist with chronic NSNP.
  • All participants will have neck pain with mobility deficit according to ICF classification of neck pain..
  • Duration of symptoms is more than 3 months to be chronic.
  • Subjects of both genders will be involved in the study.
  • Subject are young adult with the age span between 18 &29 years because this period is characterized by extensive changes, handling choices and opportunities such as moving out from home, choice of education and career, and establishing an adult lifestyle.
  • All participants will be selected with body mass index (BMI) between 18.5 and 24.9kg/cm2 which is considered the normal range of BMI.

Exclusion criteria:

  • History of cervical surgery.
  • Whiplash injuries.
  • Inflammatory arthropathy.
  • Myelopathy.
  • If neck pain is associated with radiculopathy.
  • Vertebrobasilar insufficiency.
  • Red flags suggesting of cancer or infection .
  • Fracture.
  • Diabetic patients.
  • Hypertensive patients.
  • Obese subjects.
  • Vertigo.
  • Thoracic outlet syndrome.

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: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Mckenzie exercises group
This group will receive Mckenzie exercises and the conventional treatment 3 sessions per week for four weeks

Fifteen participants will receive Mckenzie exercises prescribed by McKenzie for cervical dysfunction from sitting position with the following progressions:

  1. Repeated movements in the direction of the dysfunction.
  2. Repeated movements with patient overpressure.
  3. Repeated movements with therapist overpressure. All exercises will be performed while maintaining retraction position with repetition of 10 to 15 times.

This group will also receive the conventional treatment prescribed for chronic Non-specific neck pain in the form of hot packs, postural correction, stretching, Isometric strengthening and scapular stabilization exercises.

Experimental: Maitland mobilization for cervical spine group
This group will receive Maitland mobilization for cervical spine and the conventional treatment 3 sessions per week for four weeks

Fifteen participants will receive Mailand mobilization for cervical spine: With one or two oscillations per second for one-minute, central postero-anterior (P/A) glide over spinous process in case of central or bilateral symptoms and unilateral postero-anterior (P/A) glide over articular process in case of unilateral symptoms. Grade 1 or 2 will be applied to relieve pain while grade 3 or 4 will be applied to increase ROM.

This group will also receive the conventional treatment prescribed for chronic Non-specific neck pain in the form of hot packs, postural correction, stretching, Isometric strengthening and scapular stabilization exercises.

Active Comparator: The onventional treatment group
This group will receive only the conventional treatment 3 sessions per week for four weeks

Fifteen 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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cervical proprioception
Time Frame: 4 weeks
Cervical proprioception will be assessed using CROM device.
4 weeks
Cervical range of motion
Time Frame: 4 weeks
Cervical ROM will be assessed using CROM device.
4 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Neck function
Time Frame: 4 weeks
Arabic version of neck disability index will be used to assess neck function
4 weeks
Pain intensity
Time Frame: 4 weeks
Numerical Rating Scale will be used to assess pain intensity
4 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 (Estimated)

December 12, 2025

Primary Completion (Estimated)

April 15, 2026

Study Completion (Estimated)

April 15, 2026

Study Registration Dates

First Submitted

December 5, 2025

First Submitted That Met QC Criteria

December 5, 2025

First Posted (Actual)

December 18, 2025

Study Record Updates

Last Update Posted (Actual)

December 18, 2025

Last Update Submitted That Met QC Criteria

December 5, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • P.T.REC/012/006047

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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