Condition: Meniere Disease · Sponsor: Abant Izzet Baysal University
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.
nurgul sarı, Master's Degree · +905344527440 · nurgulsen12@gmail.com
omer pala, associate professor · +905327975716
Always discuss trial participation with your own doctor first.
| Afyonkarahisar Health Sciences University Health Application and Research Center, Ear, Nose and Throat Polyclinic | Afyonkarahisar, Afyonkarahisar, Turkey (Türkiye) | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07272473