- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04793763
Comparing the Effect of Deep Neck Flexors Versus MCkenice Exercises on Cervical Functions (McKENICE)
Comparing the Effect of Deep Neck Flexors and MCkenice Exercises on Cervical Mobility,Pain and Disability in Chronic Neck Pain Participants
Study Overview
Status
Conditions
Detailed Description
This study will be a randomized controlled trial that involved sixty patients of both gender with chronic neck pain with duration of at least six weeks that will be recruited into the study. They will be recruited from the out patient clinic of Faculty of Physical Therapy, Egypt ,their age ranged from (30-50) years old with mean age, their height ranged from (152-182) cm and their weight ranged from (55-90) kg , Patients will be included if they had a localized chronic neck pain without any current arm pain or discomfort were included.Groups:
A: twenty patients will receive traditional Physical Therapy agents, Group B: twenty patients will receive traditional Physical Therapy agents plus isometric, stretching, scapulothoracic exercises and deep neck flexors exercises; and Group C: twenty patients will receive traditional Physical Therapy agents plus isometric, stretching, scapulothoracic exercises and Mckenzie technique.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Reham H Diab, profeessor
- Phone Number: 00201006195473
- Email: reham.diab@yahoo.com
Study Contact Backup
- Name: Rania R mohammed, lecturer
- Phone Number: 00201273325285
- Email: raniareda22@Hotmail.com
Study Locations
-
-
-
Giza, Egypt, 12662
- Recruiting
- Faculity of Physical Therapy
-
Contact:
- Reham H Diab, PH.D
- Email: reham.diab@yahoo.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- age ranges from (30-50) years old with mean age,
- height ranges from (152-182) cm and their weight ranged from (55-90) kg
- Patients will be included if they have a localized chronic neck pain without any current arm pain or discomfort were included.
Exclusion Criteria:
- history of cervical spine injury or surgery, if neck pain is secondary to other conditions (including neoplasm, neurological diseases or vascular diseases),
- they have a radiculopathy presenting neurological deficit
- they had infection or inflammatory arthritis in the cervical spine,
- they have pain with any cause in or around the scapula, shoulder, upper extremities and lumbar spine that prevents stabilization of these structures.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Placebo Comparator: group A
placebo Comparator Group A : twenty patients were received traditional Physical Therapy agents |
group A will receive traditional exercises
|
Experimental: group B
experimental Group B Group B: twenty patients were received traditional Physical Therapy agents plus isometric, stretching, scapulothoracic exercises and deep neck flexors exercises;
|
Group B will receive traditional therapeutic exercises and McKenize technique
|
Experimental: group C
Experimental Group C Group C: twenty patients were received traditional Physical Therapy agents plus isometric, stretching, scapulothoracic exercises and Mckenzie technique. |
Group C receive traditional therapeutic exercises and deep neck flexor exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
neck functional activity
Time Frame: after 6 weeks
|
The Copenhagen neck capacity inability scale
|
after 6 weeks
|
pain disability
Time Frame: after 6 weeks
|
VAS
|
after 6 weeks
|
cervical range of motion
Time Frame: after 6 weeks
|
use Myrin goniometer
|
after 6 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Amr A Abd el aziem, professor, Cairo University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/003053
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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