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Completed

NCT Number: NCT04687371

The Effect of Proprioseptive Vestibular Rehabilitation in Patients With Peripheral Vestibular Hypofunction

The aim of this study was to investigate the effect of proprioceptive vestibular rehabilitation on balance, functional mobility, posture, sensory profile and quality of life in patients with vertigo due to peripheral vestibular hypofunction.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Inonu University

Malatya, Battalgazi/MALATYA, 44280, Turkey (Türkiye)

About this study

Peripheral vestibular system; It forms the part extending from the structures in the inner ear to the vestibular nuclei in the brainstem. Peripheral vestibular hypofunction is a chronic disease affecting one or both sides of the vestibular system, which occurs when the function of the vestibular organs, vestibular nerve, or both is reduced or destroyed. Many patients with peripheral vestibular hypofunction develop symptoms such as dizziness, vertigo, imbalance, gait disturbance. Many different exercise methods have been tried so far to relieve these symptoms and increase the functionality of the patient. In this study, we aimed to examine the effect of proprioceptive vestibular rehabilitation on balance, quality of life, posture, sensory profile and functional mobility in patients with vertigo due to peripheral vestibular hypofunction aged 18-65 years. Patients with vertigo due to peripheral vestibular hypofunction between the ages of 18-65 will be included in our study. The population of the research will be created by the cluster sampling method and the randomization of the patients to be recruited will be determined using the "research ramdomizer" computer program; Patients will be divided into 3 groups as experimental and control groups. A randomized controlled, single-blind study will be planned. Group I (experiment): Glance stabilization exercises, Cawthorne Cooksey Exercises and Proprioceptive vestibular rehabilitation exercises, Group II (experiment): Glance stabilization exercises and Cawthorne Cooksey Exercises and Group III (control): no exercise will be given, they will be asked to continue daily life. Exercises will be applied to each group for 8 weeks, 4 days a week, 30 minutes, in the presence of 1 set of physiotherapists and as a home exercise program every day of the week. Individuals will be evaluated before and 8 weeks after the treatment. Tinetti Balance Test for balance assessment, One leg stand test; timed up and go test for functional mobility assessment; Dizziness Disability Inventory for quality of life; mobile posture assessment application for posture assessment; Adult / Adolescent Sensory profile will be used for sensory assessment. Pre- and post-treatment and intergroup evaluations will be compared, and the effectiveness of proprioceptive vestibular rehabilitation on balance, functional mobility, posture, sensory profile and quality of life, and its superiority over standard exercises will be interpreted.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Between 18-65 years
  • Diagnosis of vertigo according to the clinical examination performed by an Otorhinolaryngologist, Vestibular Evoked Myogenic Potentials (VEMP), Video Head Impulse Test (VHIT)
  • Patients with Unilateral Peripheral Hypofunction
  • After giving detailed information about the research, agreeing to participate in the study.

Exclusion criteria

  • Severe hearing / vision impairment-loss
  • Patients with neurological, orthopedic, circulatory system problems that may cause vertigo, dizziness and balance disorders
  • Having severe hypertension / diabetes
  • Previous participation in a vestibular rehabilitation program
  • Being healthy
  • Patients using drugs that may affect the treatment negatively
  • Refusing to participate in a clinical trial
  • Patients who cannot adapt to the training program
  • Patients who discontinued their treatment
  • Patients with different diagnoses that may disrupt the treatment during the study

Treatment and study plan

Proprioceptive vestibular exercise

Other

To assess effects of proprioceptive vestibular exercises training in patients with peripheral vestibular hypofunctions

Other names: Cawthorne cooksey exercises, Gaze stabilization exercises

Standard vestibular rehabilitation exercises

Other

To assess effects of standard vestibular rehabilitation exercises in patients with peripheral vestibular hypofunctions

Other names: Cawthorne Cooksey Exercises, Gaze Stabilization Exercises

Controlled

Other

First and last measurement will be taken. There will be no intervention. study will include 9 patients.

Primary outcomes

  1. Dizziness handicap inventory

    Time frame: 8 weeks

    It used to assess the quality of life in patients with vertigo

  2. Tinetti balance test

    Time frame: 8 weeks

    It used to asses the balance (questionnaire, score)

  3. Time up and go test

    Time frame: 8 weeks

    It used to assses the functionality (sec)

  4. Adolescent/Adult Sensory Profile

    Time frame: 8 weeks

    In the test, 6 different sensory processing processes are evaluated. Includes assessments of taste/smell process, movement process, visual processing, touch process, activity level and auditory processing. Each item is scored with likert measurements between 1 and 5 points determined by the person.

  5. Mobile application for Posture Analyze

    Time frame: 8 weeks

    It used to assess Posture (Degree)

Sponsors and collaborators

Lead sponsor

Inonu University

Other

Registry information

Official study title

The Effect of Proprioseptive Vestibular Rehabilitation on the Balance, Functional Mobility, Posture, Sensory Profile and Quality of Life in Patients With Vertigo Due to Peripheral Vestibular Hypofunction

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Dec 29, 2020
Registry last updated
Apr 19, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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