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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04367194
Other study ID # IKEB2019/15
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 23, 2018
Est. completion date June 23, 2020

Study information

Verified date January 2021
Source Somogy Megyei Kaposi Mór Teaching Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 2
Est. completion date June 23, 2020
Est. primary completion date June 23, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 45 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Neurorehabilitation
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.

Locations

Country Name City State
Hungary Somogy Megyei Kaposi Mór Oktató Kórház Kaposvár Somogy

Sponsors (1)

Lead Sponsor Collaborator
Somogy Megyei Kaposi Mór Teaching Hospital

Country where clinical trial is conducted

Hungary, 

Outcome

Type Measure Description Time frame Safety issue
Primary EQ5D-5L 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. 5 weeks
Primary Beam Walking test 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. 5 weeks
Primary Posturography Noninvasive intervention where static equilibrium is examined. The program determines the quality and frequency of the displacements. 5 weeks
See also
  Status Clinical Trial Phase
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Not yet recruiting NCT04283084 - Development and Evaluation of Balance and Coordination Training System N/A
Completed NCT03952936 - Vestibular Rehabilitation for Chronic Central Vestibular Deficits: A Case Study N/A
Completed NCT05226715 - Effect of Lower Extremity Joint Manipulation on a Lower Extremity Somatosensory Illusion N/A
Completed NCT04220541 - Investigation of the Effects of Exercise on Patients With Chiari Malformation N/A

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