- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07290374
Mckenzie Versus Maitland Cervical Mobilization Technique in Management of Non-specific Neck Pain.
Study Overview
Status
Conditions
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Mahmoud Salah Abd-elfattah, Assistant lecturer
- Phone Number: +201068419431
- Email: mahmoud.salah@cu.edu.eg
Study Contact Backup
- Name: Mahmoud Salah Abd-Elfattah, Assistant lecturer
- Phone Number: 01068419431
- Email: mahmoud.salah@cu.edu.eg
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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:
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:
|
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
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/006047
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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