NCT07502625

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

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
62

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started Apr 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress62%
Apr 2026Aug 2026

First Submitted

Initial submission to the registry

March 24, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 31, 2026

Completed
1 day until next milestone

Study Start

First participant enrolled

April 1, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Last Updated

March 31, 2026

Status Verified

March 1, 2026

Enrollment Period

3 months

First QC Date

March 24, 2026

Last Update Submit

March 27, 2026

Conditions

Keywords

Cervical spondylosisEvoked myogenic potentialsVestibular rehabilitation

Outcome Measures

Primary Outcomes (3)

  • Primary outcome

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

    base line and after 2 months

  • Primary outcomev

    Balance will be assessed using HUMAC balance system.

    base line and after 2 months

  • Primary outcome

    Cervical proprioception will be assessed using SenMoCOR Laser Head Light.

    base line and after 2 months

Secondary Outcomes (2)

  • Secondary outcome

    base line and after 2 months

  • Secondary outcome

    base line and after 2 months

Study Arms (2)

Experimental group

EXPERIMENTAL

Experimental group will receive Vestibular rehabilitation program plus TENS and Hot Pack application, it will be done three times per week for two months

Other: Vestibular rehabilitation program

Control group

ACTIVE COMPARATOR

control group will receive TENS and hot packs,it will be done three times per week for two months

Other: traditional physiotherapy

Interventions

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

Experimental group

TENS and Hot packs application

Control group

Eligibility Criteria

Age40 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • 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).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Spondylosis

Condition Hierarchy (Ancestors)

Spinal DiseasesBone DiseasesMusculoskeletal Diseases

Central Study Contacts

Salah Eid Ahmed Ali, Ph D

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Lecturer

Study Record Dates

First Submitted

March 24, 2026

First Posted

March 31, 2026

Study Start

April 1, 2026

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

August 1, 2026

Last Updated

March 31, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share