McKenzie and ELDOA Comparison in Non-Specific Neck Pain Teachers

August 18, 2025 updated by: Riphah International University

Comparison of McKenzie Protocol and ELDOA in Teachers With Non-Specific Neck Pain

The aim of this study is to compare the effectiveness of McKenzie Protocol and ELDOA on severity of pain, on the range of motion and disability level of teachers with Non-Specific neck pain.

Study Overview

Detailed Description

Neck pain, a common musculoskeletal condition and a common problem of the society, is "a pain originating from musculoskeletal tissue in the region from the Occiput to the First Thoracic Vertebrae". Approximately 2/3 of the population around Globe is affected by Neck Pain as it is the 4th leading cause of disability around the world. Several research has shown prevalence ranging between 14.2% to 71%, with increased frequency in females and middle-aged adults. Risk factors related to neck pain generally constitute trauma or sports related injuries, poor work environment and psychological issues. This common problem can further be categorized based on duration i.e. Acute (for less than 6 weeks), Sub Acute (for less than 3 months) and Chronic (For more than 3 months). Based on severity, it is further sub-divided into 3 categories (Mild, Moderate and Severe). Based on etiology it has 2 types, (Mechanical and Neuropathic) Non-Specific Neck pain (NNP), a broader term used, is a common appearance of Neck Pain elaborated as Pain without any defined cause. It can either be a Mechanical or a Postural complication. Non-Specific Neck pain can be diagnosed from the history of individual along with physical examination. Non-Specific Neck Pain responds to conservative management, but the recent Literature suggests that Exercise therapy is quite effective in treatment of Non-specific Neck Pain (NNP). Techniques include Exercise therapy, Manual therapy, Traction, Electrotherapeutic modalities, Stretching, Massage, Release Techniques (ARTs) which are effective not only for reducing Pain but also for improving Cervical Ranges and functional capacity of Individuals.

Teaching is considered among those Professions where Incidence of Neck pain is at its peak, a recent Literature suggest that Prevalence of Neck pain is 68.9% in teachers. Occupational Complications i.e. Long-standing hours, Faulty postures, Excessive use of electronic devices and Black boards are the major risk factors for teachers in developing Musculoskeletal Conditions, with an incidence of 40% to 95%.

McKenzie Protocol is an interventional approach used in the broader term of Exercise Therapy. A Literature published in International Journal of Physiotherapy and Research by researchers of Cairo University, Egypt showed that McKenzie Protocol is very effective for the treatment of Non-specific Spinal Pain. This technique encourages active patient involvement in decreasing pain which as a result increases the functional abilities of individuals. The Technique of Neck Retraction is very beneficial for increasing Cervical Ranges, improving Posture and relieving Neck pain. McKenzie Protocol is a very effective technique for preventing re-occurrence of Pain.

ELDOA an abbreviation used for a French acronym Elongation Longitudinaux avec Decoaption Osteo-Articulaire is a term described by Guy Voyer in 1979 as an active Traction technique used for stretching of Fascia and increasing Spacing of Spinal joints. Literature backs the claim that ELDOA is an effective technique used to decrease pain and increasing Muscle length. This technique release compression from the Facet joints which in return increase circulation and improves tone that helps in Pain reduction and Range improvement.

Neck Pain frequently affects teachers due to Occupational habits. According to the Global Burden of Disease (GBD) Study, neck pain is the second leading cause of years lived with disability (YLD) for adults, 50% - 75% of people do not recover from an acute episode and experience recurrent neck pain in the next 1 to 5 years. Approximately 68% of people develop persistent and chronic neck pain. A Meta-analysis focusing on the McKenzie Protocol indicated its efficacy in managing moderate to severe neck pain, relative to mild cases. Various studies have explored the individual effects of McKenzie and ELDOA techniques on Neck pain. However, no one has specifically investigated which protocol is more effective across different severity levels.

Study Type

Interventional

Enrollment (Actual)

36

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
      • Islamabad, Punjab, Pakistan, 46000
        • Yusra Medical and Dental College

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:

  • Normal BMI
  • Neck Pain on NPRS (Mild 1-3, Moderate 4-6, Severe 7-10)
  • Working Hour: At least 30 hrs. per week.
  • Teaching Experience: More than 12 months

Exclusion Criteria:

  • No Neurological Condition (+ve Spurling Test, +ve Compression test, +ve Distraction Test)
  • No Other Musculoskeletal Condition. (Osteoporosis, Arthritis, TrPs)
  • No Spinal Deformity. (Scoliosis, Forward Head)
  • No Surgery (Spinal Surgery, Fracture)
  • No Cervical Tumor
  • No complaints about Dizziness, Migraine, Cervicogenic headache (+ve Flexion Rotation test)

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: ELDOA + Conventional PT

ELDOA, the protocol consists of 4 positions. Each position is maintained for 1 min with constant correction of posture throughout with 2 to 4 min rest within each position. The Exercise was performed in 10 to 25 mins. 4 positions of ELDOA are Decoarctation of C0/C1/C2, Decoarctation of C4/C5, Decoarctation of C5/C6, Decoarctation of C6/C7. All positions are attained in lying.

Hot pack 2. isometric strengthening exercises (Neck Flexion, Extension and Lateral Flexion) in 3x5 sets with 5 sec hold.

ELDOA, the protocol consists of 4 positions. Each position is maintained for 1 min with constant correction of posture throughout with 2 to 4 min rest within each position. The Exercise was performed in 10 to 25 mins. 4 positions of ELDOA are Decoarctation of C0/C1/C2, Decoarctation of C4/C5, Decoarctation of C5/C6, Decoarctation of C6/C7. All positions are attained in lying.

Hot pack 2. isometric strengthening exercises (Neck Flexion, Extension and Lateral Flexion) in 3x5 sets with 5 sec hold.

Active Comparator: McKenzie Protocol + Conventional PT

Extension Dysfunction Retraction Retraction with patient overpressure Retraction with therapist overpressure Retraction with extension

Lateral Flexion Dysfunction

Lateral flexion:

Lateral flexion with patient overpressure Lateral flexion therapist overpressure

Rotation Dysfunction Rotation Rotation with patient overpressure

Hot pack, isometric strengthening exercises (Neck Flexion, Extension and Lateral Flexion) in 3x5 sets with 5 sec hold Rotation with therapist overpressure

Extension Dysfunction Retraction Retraction with patient overpressure Retraction with therapist overpressure Retraction with extension Lateral Flexion Dysfunction Lateral flexion: Lateral flexion with patient overpressure Lateral flexion therapist overpressure Rotation Dysfunction Rotation Rotation with patient overpressure Hot pack, isometric strengthening exercises (Neck Flexion, Extension and Lateral Flexion) in 3x5 sets with 5 sec hold Rotation with therapist overpressure

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Range of motion (Goniometer)
Time Frame: 3 weeks
It is the most common instrument used to measure the range of motion of joints across the whole body. Normal ranges of cervical spine are Flexion approximately 80°, Extension 50°, Lateral bending 45° on either side and Rotation approximately 80°. Its Reliability (ICC = 0.82) and Validity (Correlations 0.97-0.98)
3 weeks
Numeric Pain Rating Scale NPRS
Time Frame: 3 weeks
The NPRS is an eleven-point pain impression scale: the patient rates pain from 0 (no aggravation) to 10 (most exceedingly terrible possible pain). Mild 1-3, Moderate 4-6, Severe 7-10. Numeric Pain Rating Scale (NPRS), which was used to survey respondents' impression of the degree of pain that they felt. It is an outcome measure that is a unidimensional measure of pain intensity in adults. It is considered a more objective and Numeric version of Visual Analogue Scale.
3 weeks
Neck Disability Index or NDI
Time Frame: 3 weeks
It has sufficient support and usefulness to retain its status as the most used self-report disability measure for neck pain. 0 to 4 = no disability, 5 to 14 = mild, 15 to 24 = moderate, 25 to 34 = severe, above 34 = complete. It has ten sections with each section carrying 5 marks.
3 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Maria khalid, MSOMPT, Riphah International University

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)

April 24, 2025

Primary Completion (Actual)

June 2, 2025

Study Completion (Actual)

June 10, 2025

Study Registration Dates

First Submitted

April 14, 2025

First Submitted That Met QC Criteria

April 14, 2025

First Posted (Actual)

April 20, 2025

Study Record Updates

Last Update Posted (Actual)

August 19, 2025

Last Update Submitted That Met QC Criteria

August 18, 2025

Last Verified

August 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/ Umul Baneen 02003

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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