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Study identifier: NCT07272473 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effects of Cervical Mobilization on Dizziness, Balance, and Joint Position Sense in Patients With Meniere's Disease

Condition: Meniere Disease  ·  Sponsor: Abant Izzet Baysal University

PhaseNA
Planned participants33
Who can joinAll sexes, 18 Years to 60 Years
Healthy volunteersNo

About this study

The study will employ a stratified randomization method. Patients presenting to the Afyonkarahisar Health Sciences University Health Application and Research Center, Ear, Nose, and Throat Outpatient Clinic, with a definitive diagnosis of Meniere's disease, unilateral or bilateral involvement, and who consent to participate in the study will be divided into three groups. The control group will receive only their routine Betahistine. Their usual treatment will remain unchanged. The first study group will receive 20 minutes of Vestibular Rehabilitation (VR) and 10 minutes of cervical mobilization in addition to their routine Betahistine. The second study group will receive 30 minutes of VR in addition to Betahistine. The study will last 6 weeks. Participants will be assessed using a sociodemographic information questionnaire, the Dizziness Handicap Inventory (DHI), the Vertigo Symptom Scale (VSS), the Neck Disability Index (NDI), the International Tinnitus Inventory (ITI), balance assessment with the K-Force Plates, and joint position sense and proprioception assessment with the Kinvent Physio K-Move. All assessments will be conducted twice, before and after treatment.

This description comes directly from the study's public registry record.

Talk to the study team

nurgul sarı, Master's Degree  ·  +905344527440  ·  nurgulsen12@gmail.com

omer pala, associate professor  ·  +905327975716

Always discuss trial participation with your own doctor first.

Locations (1)

Afyonkarahisar Health Sciences University Health Application and Research Center, Ear, Nose and Throat PolyclinicAfyonkarahisar, Afyonkarahisar, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07272473