Effect of Vestibular Rehabilitation on Evoked Myogenic Potentials in Patients With Cervical Spondylosis

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40-60
SponsorCairo University

About this trial

This study will Investigate the effect of vestibular rehabilitation on:

Primary outcomes: Vestibular evoked myogenic potentials, Balance,and Cervical proprioception.

Secondary outcomes: Functional disability and pain intensity level

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients (40-to-60 years old) diagnosed as cervical spondylosis with vestibular dysfunction manifestation (Shi et al., 2024).

Normal BMI 20-to-25 kg/m².

All patients have chronic neck pain lasting for more than 3 months (Sadeghi et al., 2022).

The area of chronic neck pain will defined to the cervical region, possibly with referred pain into the occipit, nuchal muscles, and shoulders.

Disqualifiers

Signs of serious pathology (e.g., rheumatoid diseases, ankylosing spondylitis, tumor),

History of cervical spine surgery,

History of trauma or fractures in cervical spine, and

Signs of vascular syndrome such as vertebrobasilar insufficiency and no usage of non steroidal anti-inflammatory drugs two weeks before treatment (Sadeghi et al., 2022).

Trial design

Design model

Parallel

Treatments tested in this trial

  • Vestibular rehabilitation program

    Other intervention

    Exercises for enhancing gaze stability, Exercises for enhancing eye movements, Exercises for enhancing postural stability, Exercises for decreasing vertigo, and Exercises for improving activities of daily living

  • traditional physiotherapy

    Other intervention

    TENS and Hot packs application

Treatment groups

62 Participants
are divided into 2 treatment groups
Group A: Experimental groupExperimental treatment 1 intervention
Group B: Control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Primary outcome

Vestibular evoked myogenic potentials will be assessed using Electromyography device to measure Cervical and Ocular vestibular evoked myogenic potentials.

Time frame
base line and after 2 months
2

Primary outcomev

Balance will be assessed using HUMAC balance system.

Time frame
base line and after 2 months
3

Primary outcome

Cervical proprioception will be assessed using SenMoCOR Laser Head Light.

Time frame
base line and after 2 months

Secondary outcomes

1

Secondary outcome

Functional disability will be assessed using Copenhagen Neck Functional Disability Scale Arabic Version.

Time frame
base line and after 2 months
2

Secondary outcome

Pain intensity level will be assessed using visual analogue scale.

Time frame
base line and after 2 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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