- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07230938
Effects of Neck Proprioception Impairment on Balance in Cervical Spondylosis Patients
The Influence of Cervical Proprioception Deficits on Postural Stability in Patients With Cervical Spondylosis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This cross-sectional observational study intends to investigate the association between cervical proprioception and postural stability in people with cervical spondylosis. Cervical proprioception promotes posture regulation by providing sensory feedback to the central nervous system. Alterations in cervical joint position sensation caused by degenerative alterations can have a negative impact on balance.
Eighty participants with clinically diagnosed cervical spondylosis will be recruited. Each participant will undergo a single evaluation session that includes cervical joint position error testing and postural stability assessment using pedobarographic analysis. Data will be collected on center of pressure sway, weight distribution, and balance parameters under various conditions.
so this study findings can help physical therapists, rehabilitation experts, and clinicians design protocols to improve proprioceptive input and postural control in people with cervical spondylosis. Furthermore, early diagnosis of proprioceptive deficits by pedobarography may enable preventive actions and lower the incidence of falls and related morbidity in this population.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: AISHA MOURAD MOHAMMED, Bachelor of physical therapy
- Phone Number: +20 1064046189
- Email: Aisha.Mourad@deltauniv.edu.eg
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Eighty-two patients with cervical spondylosis, the patient will be diagnosed and referred by physician.
- Mild to moderate cervical disability according to neck disability index( MacDermid et al., 2009).
- Age ranges from 25 to 45 years.
- Body mass index from 18.5 - 24.9.
Exclusion Criteria:
- The patients will be excluded if they have one of the following:
- visual or vestibular sensory disorders or cerebellar disease.
- Cervical myelopathy.
- Patients with previous cervical surgery.
- inflammatory diseases involving cervical spine such as rheumatoid arthritis or ankylosing spondylitis.
- History of cervical trauma including whiplash associated disorders (WAD).
- History of cervical tumors.
- History of ankle instability.
- No previous foot and ankle surgery.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postural stability measured using a foot pressure platform
Time Frame: Single assessment at baseline (Day 1)
|
Postural stability will be assessed by measuring postural sway using a force platform (stabilometer) under two conditions (eyes open and eyes closed).
The primary variable will be the ellipse surface area (mm²) representing the center of pressure sway.
|
Single assessment at baseline (Day 1)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cervical joint position error (JPE) measured using overhead laser pointer
Time Frame: Single assessment at baseline (Day 1)
|
Cervical proprioception will be measured using a laser pointer repositioning test.
Participants will perform active neck movements and attempt to return to the neutral position with eyes closed.
The average deviation (in degrees) from the starting point over three trials will be recorded.
Errors greater than 4.5° will indicate proprioceptive impairment
|
Single assessment at baseline (Day 1)
|
Collaborators and Investigators
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
Other Study ID Numbers
- F.P.T250794
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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