Objective Examination and Rehabilitation Treatment of Patients With BPPV
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Status
Sponsors
Somogy Megyei Kaposi Mór Teaching Hospital
CLINICAL TRIAL: NCT04367194
BioSeek: nct04367194
Keywords
Abstract
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.
Dates
Last Verified: | 03/31/2020 |
First Submitted: | 04/22/2020 |
Estimated Enrollment Submitted: | 04/25/2020 |
First Posted: | 04/28/2020 |
Last Update Submitted: | 04/25/2020 |
Last Update Posted: | 04/28/2020 |
Actual Study Start Date: | 04/22/2020 |
Estimated Primary Completion Date: | 04/22/2020 |
Estimated Study Completion Date: | 06/22/2020 |
Condition or disease
Postural Vertigo
Vertigo, Paroxysmal
Vertigo, Positional
Coordination Disorder, Developmental
Coordination and Balance Disturbances
Intervention/treatment
Behavioral: BPPV intervention
Phase
-
Arm Groups
Arm | Intervention/treatment |
---|---|
Experimental: BPPV intervention 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. | Behavioral: BPPV intervention 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. |
No Intervention: BPPV controll After the patient survey, patients received only basic treatment. | |
No Intervention: Healthy controll They do not perform therapy, they function only as a control group. |
Eligibility Criteria
Ages Eligible for Study | 18 Years To 18 Years |
Sexes Eligible for Study | All |
Accepts Healthy Volunteers | Yes |
Criteria | 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 |
Outcome
Primary Outcome Measures
1. EQ5D-5L [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 [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 [5 weeks]
Noninvasive intervention where static equilibrium is examined. The program determines the quality and frequency of the displacements.