Impact of Craniovertebral Angle on Dizziness and Risk of Falling in Cervical Radiculopathy Patients

January 14, 2024 updated by: Sara Abdelrahman Elsayed Hassan Aboud, Cairo University

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

Recruiting

Study Type

Observational

Enrollment (Estimated)

50

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Giza Governorate
      • Dokki, Giza Governorate, Egypt, 12612
        • Recruiting
        • Faculty of Physical Therapy labs at Cairo University
        • Contact:
        • Contact:
          • Faculty of Physical Therapy Labs at Cairo University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Fifty patients with chronic cervical radiculopathy(degenerative type) from both sex will be enrolled in this study. Patients will be assigned into two groups (study and control groups) . The Study group (GI) will include twenty five patients with chronic cervical radiculopathy with forward head posture (FHP) (CVA=less than 49° ). Control group (GII) will include twenty five patients with chronic cervical radiculopathy without forward head posture (FHP)( CVA =more than 49°). Patients in group I were diagnosed as patients with chronic cervical radiculopathy with forward head posture (FHP) based on careful clinical evaluation by the neurologist . The patients will be recruited from the faculty of Physical Therapy, Cairo University, and private clinic in cairo .

Description

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 Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
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° ).
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).

What is the study measuring?

Primary Outcome Measures

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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 4, 2023

Primary Completion (Estimated)

January 29, 2024

Study Completion (Estimated)

January 29, 2024

Study Registration Dates

First Submitted

January 14, 2024

First Submitted That Met QC Criteria

January 14, 2024

First Posted (Actual)

January 24, 2024

Study Record Updates

Last Update Posted (Actual)

January 24, 2024

Last Update Submitted That Met QC Criteria

January 14, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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