Effects of Neck Proprioception Impairment on Balance in Cervical Spondylosis Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age25-50
SponsorDelta University for Science and Technology

About this trial

This observational cross-sectional study aims to investigate the impact of cervical proprioception deficits on postural stability in patients with cervical spondylosis. Using pedobarographic analysis, the study will assess static balance parameters in affected individuals. The main question it aims to answer is: Does Cervical proprioception deficits affect postural stability in patients with cervical spondylosis measured by pedobarographic parameters?

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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.

Trial population

Eighty-two patients with cervical spondylosis will represent the sample of this study. They will be selected from the outpatient clinic of Faculty of Physical Therapy, Delta University. All the patients will sign a consent form before starting the study

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Pedobarography system (foot pressure plateform)

    Device

    Pedobarography system (foot pressure plateform) for Postural Stability assessment will be used to assess Postural stability. the pedobarographic analysis will be delivered using the FreeMed Professional platform (Sensor Medica, Rome, Italy). It evaluates the distribution of foot pressure on the ground.Three components make up the platform: a central mat with resistance sensors and two passive mats at either end that form a walking path. The platform is connected to a computer, to which all data is displayed and processed using FreeStep software

  • overhead laser pointer

    Device

    laser pointer for Cervical proprioception device will be used to assess cervical proprioception by preforming Cervical joint position error (JPE) test

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Postural stability measured using a foot pressure platform

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.

Time frame
Single assessment at baseline (Day 1)

Secondary outcomes

1

Cervical joint position error (JPE) measured using overhead laser pointer

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

Time frame
Single assessment at baseline (Day 1)

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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