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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06220799
Other study ID # P.T.REC/012/004743
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 4, 2023
Est. completion date January 29, 2024

Study information

Verified date January 2024
Source Cairo University
Contact Sara Aboud, Teaching Assistant
Phone +201003194513
Email saraaboud1994@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

-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 .


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date January 29, 2024
Est. primary completion date January 29, 2024
Accepts healthy volunteers No
Gender All
Age group 35 Years to 50 Years
Eligibility Inclusion Criteria: - The Patients will include if they have the following: 1. 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) ). 2. The duration of the disease (cervical radiculopathy)is more than 6 months. 3. The age ranged from 35 to 50 years old. 4. Mild to moderate neck pain on visual analogue scale . 5. Pain and dizziness lasting for 3-6 months. 6. 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: 1. Cervical myelopathy. 2. Cervical myelo-radiculopathy. 3. Acute cervical radiculopathy. 4. Diabetic neuropathy. 5. Previous cervical surgery. 6. Cervical trauma. 7. Deformities in the cervical spine . 8. Rheumatoid arthritis. 9. Any tumours and infection involving the cervical spine . 10. Patients with a history of neuromuscular disorders. 11. 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 Design


Related Conditions & MeSH terms


Locations

Country Name City State
Egypt Faculty of Physical Therapy Labs at Cairo University Dokki Giza Governorate

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Craniovertebral angle (CVA) Taking photos from lateral view then craniovertebral angle measured by Kinovea software program. 20 minutes
Primary Cervical joint position error . Cervical joint position error via the CROM device,through the neutral head repositioning test (NHR) and the target head repositioning test (THR). 40 minutes
Primary Cervicogenic dizziness. Cervicogenic dizziness via score of Dizziness Handicap Inventory Questionnaire(DHI). 10 minutes
Primary The risk of falling. The risk of falling assessed by Berg Balance Scale(BBS) . 20 minutes
Primary The fear of falling. The fear of falling assessed by Fall Efficacy Scale-International(FES-I). 10 minutes
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