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

Status

Not yet recruiting

Phases

Unknown

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT07502625

Enrollment

Registered

2026-03-31

Start date

2026-04-01

Completion date

2026-08-01

Last updated

2026-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Spondylosis

Keywords

Cervical spondylosis, Evoked myogenic potentials, Vestibular rehabilitation

Brief summary

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

Interventions

OTHERVestibular rehabilitation program

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

OTHERtraditional physiotherapy

TENS and Hot packs application

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender

ALL

Age

40 Years to 60 Years

Healthy volunteers

Inclusion criteria

* 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.

Exclusion criteria

* 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).

Design outcomes

Primary

Measure	Time frame	Description
Primary outcome	base line and after 2 months	Vestibular evoked myogenic potentials will be assessed using Electromyography device to measure Cervical and Ocular vestibular evoked myogenic potentials.
Primary outcomev	base line and after 2 months	Balance will be assessed using HUMAC balance system.

Secondary

Measure	Time frame	Description
Secondary outcome	base line and after 2 months	Functional disability will be assessed using Copenhagen Neck Functional Disability Scale Arabic Version.

Contacts

CONTACTSalah Eid Ahmed Ali, Ph D

salaheid7@gmail.com+201158125773

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026