NCT07290374

Brief Summary

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.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
45

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2025

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 5, 2025

Completed
7 days until next milestone

Study Start

First participant enrolled

December 12, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

December 18, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 15, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 15, 2026

Completed
Last Updated

December 18, 2025

Status Verified

December 1, 2025

Enrollment Period

4 months

First QC Date

December 5, 2025

Last Update Submit

December 5, 2025

Conditions

Keywords

MaitlandMckenzieneck pain

Outcome Measures

Primary Outcomes (2)

  • Cervical proprioception

    Cervical proprioception will be assessed using CROM device.

    4 weeks

  • 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)

Mckenzie exercises group

EXPERIMENTAL

This group will receive Mckenzie exercises and the conventional treatment 3 sessions per week for four weeks

Other: Mckenzie exercises

Maitland mobilization for cervical spine group

EXPERIMENTAL

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

Other: Maitland mobilization for cervical spine

The onventional treatment group

ACTIVE COMPARATOR

This group will receive only the conventional treatment 3 sessions per week for four weeks

Other: The conventional treatment group

Interventions

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.

Maitland mobilization for cervical spine group

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.

The onventional treatment group

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.

Mckenzie exercises group

Eligibility Criteria

Age18 Years - 29 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Mahmoud Salah Abd-elfattah, Assistant lecturer

CONTACT

Mahmoud Salah Abd-Elfattah, Assistant lecturer

CONTACT

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

December 5, 2025

First Posted

December 18, 2025

Study Start

December 12, 2025

Primary Completion

April 15, 2026

Study Completion

April 15, 2026

Last Updated

December 18, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share