Skip to main content
OpenTrials
Completed

NCT Number: NCT04367194

Objective Examination and Rehabilitation Treatment of Patients With BPPV

Dizziness (BPPV) causes severe deterioration in quality of life, incoordination, and instability.

In the study, we selected a minimum of 100 patients with BPPV who were examined after specialist care. After the acute phase, a physical survey is performed where movement and coordination are examined.

After the results, the patients undergo a rehabilitation training. The workout is submaximal and high intensity that is done for 3 weeks.

Hypothesis: As a result of training, it is possible that the remaining feeling of dizziness and insecurity, impaired coordination will decrease or disappear.

Completed

Looking for future studies?

Notify Me

Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • For a patient with BPPV
  • With a lack of coordination
  • Dizziness
  • Ear nose laryngeal examination
  • Neurological examination

Exclusion criteria

  • other neurological diseases
  • cardiological diseases
  • underwent surgery
  • severe joint pain
  • alcoholism
  • dementia
  • drug

Treatment and study plan

Neurorehabilitation

Behavioral

After examination of the patients, the patients undergo neurorehabilitation. We use virtual reality therapy. Patients perform a submaximal load that is monitored by a polar clock. We develop endurance, coordination, sensory integration, visual and acoustic input, vestibular training, proprioception training.

Other names: BPPV group

Primary outcomes

  1. EQ5D-5L

    Time frame: 5 weeks

    Quality of life testing is taken with a test. The therapist scores the answers to the questions asked on a scale. The end result determines the quality of life.

  2. Beam Walking test

    Time frame: 5 weeks

    The patient walks on slats of varying width. During the examination, the therapist says the tasks (Eg: counting backwards). The study detects the determination of dynamic equilibrium.

  3. Posturography

    Time frame: 5 weeks

    Noninvasive intervention where static equilibrium is examined. The program determines the quality and frequency of the displacements.

Sponsors and collaborators

Lead sponsor

Somogy Megyei Kaposi Mór Teaching Hospital

Other

Registry information

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Apr 29, 2020
Registry last updated
Jan 14, 2021

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.

Published trials that share one or more normalized conditions with this study.