- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06220799
Impact of Craniovertebral Angle on Dizziness and Risk of Falling in Cervical Radiculopathy Patients
Impact of the Craniovertebral Angle on the Cervicogenic Dizziness and the Risk of Falling in Patients With Cervical Radiculopathy
-The goal of this observational study is to learn about the impact of the changes in cranio-vertebral angle on the cervicogenic dizziness and the risk of falling in the patients with cervical radiculopathy .The main question it aims to answer is: Is there an impact of the changes in cranio-vertebral angle on the cervicogenic dizziness and the risk of falling in the patients with cervical radiculopathy ? The participants will be undergone measuring the cranio-vertebral angle ,assessment of cervical proprioception and other tasks and questions through 3scales .
Researchers will compare between study group and control group to see if there isimpact of the changes in cranio-vertebral angle on the cervicogenic dizziness and the risk of falling in the patients with cervical radiculopathy .
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Sara Aboud, Teaching assistant
- Phone Number: +201003194513
- Email: saraaboud1994@gmail.com
Study Contact Backup
- Name: Ashraf Darwesh, Assistant Professor
- Phone Number: +201111462073
- Email: ashraf.darwesh@cu.edu.eg
Study Locations
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Giza Governorate
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Dokki, Giza Governorate, Egypt, 12612
- Recruiting
- Faculty of Physical Therapy labs at Cairo University
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Contact:
- Sara Aboud, Teaching assistant
- Phone Number: +201003194513
- Email: saraaboud1994@gmail.com
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Contact:
- Faculty of Physical Therapy Labs at Cairo University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
The Patients will include if they have the following:
- Fifty patients with chronic cervical radiculopathy(degenerative type) from both sex will participate in the study (twenty five with forward head posture (FHP) , and twenty five without forward head posture (FHP) ).
- The duration of the disease (cervical radiculopathy)is more than 6 months.
- The age ranged from 35 to 50 years old.
- Mild to moderate neck pain on visual analogue scale .
- Pain and dizziness lasting for 3-6 months.
subjective dizziness experienced in conjunction with cervical pain, movement, stiffness, or particular postures.
Exclusion Criteria:
The Patients will exclude if they exhibit any of the following:
- Cervical myelopathy.
- Cervical myelo-radiculopathy.
- Acute cervical radiculopathy.
- Diabetic neuropathy.
- Previous cervical surgery.
- Cervical trauma.
- Deformities in the cervical spine .
- Rheumatoid arthritis.
- Any tumours and infection involving the cervical spine .
- Patients with a history of neuromuscular disorders.
- precise diagnosis of either central dizziness (due to cerebrovascular disorders related to the vertebrobasilar circulation, migraine, multiple sclerosis, tumours of the posterior fossa, neurodegenerative disorders, some drugs, and psychiatric disorders) or peripheral dizziness( due to a problem in the part of the inner ear that controls balance. These areas are called the vestibular labyrinth, or semicircular canals. The problem may also involve the vestibular nerve. This is the nerve between the inner ear and the brain stem).
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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The Study group (GI)
The Study group (GI) will include twenty five patients with chronic cervical radiculopathy with forward head posture (FHP) (CVA=less than 49° ).
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The Control group (GII)
The Control group (GII) will include twenty five patients with chronic cervical radiculopathy without forward head posture (FHP)( CVA = more than 49).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Craniovertebral angle (CVA)
Time Frame: 20 minutes
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Taking photos from lateral view then craniovertebral angle measured by Kinovea software program.
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20 minutes
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Cervical joint position error .
Time Frame: 40 minutes
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Cervical joint position error via the CROM device,through the neutral head repositioning test (NHR) and the target head repositioning test (THR).
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40 minutes
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Cervicogenic dizziness.
Time Frame: 10 minutes
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Cervicogenic dizziness via score of Dizziness Handicap Inventory Questionnaire(DHI).
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10 minutes
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The risk of falling.
Time Frame: 20 minutes
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The risk of falling assessed by Berg Balance Scale(BBS) .
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20 minutes
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The fear of falling.
Time Frame: 10 minutes
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The fear of falling assessed by Fall Efficacy Scale-International(FES-I).
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10 minutes
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
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/012/004743
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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