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Objective Examination and Rehabilitation Treatment of Patients With BPPV

Primary Purpose

Postural Vertigo, Vertigo, Paroxysmal, Vertigo, Positional

Status
Completed
Phase
Not Applicable
Locations
Hungary
Study Type
Interventional
Intervention
Neurorehabilitation
Sponsored by
Somogy Megyei Kaposi Mór Teaching Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postural Vertigo focused on measuring vertigo, balance, instability, rehabilitation

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Somogy Megyei Kaposi Mór Oktató Kórház

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

BPPV intervention

BPPV Epley

BPPV Optocinetic

Arm Description

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.

Only Epley training.

Only Optocinetic training.

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Full Information

First Posted
April 23, 2020
Last Updated
January 11, 2021
Sponsor
Somogy Megyei Kaposi Mór Teaching Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04367194
Brief Title
Objective Examination and Rehabilitation Treatment of Patients With BPPV
Official Title
Objective Examination and Rehabilitation Treatment of Patients With BPPV
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
April 23, 2018 (Actual)
Primary Completion Date
June 23, 2020 (Actual)
Study Completion Date
June 23, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Somogy Megyei Kaposi Mór Teaching Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postural Vertigo, Vertigo, Paroxysmal, Vertigo, Positional, Coordination Disorder, Developmental, Coordination and Balance Disturbances
Keywords
vertigo, balance, instability, rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
BPPV intervention
Arm Type
Experimental
Arm Description
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.
Arm Title
BPPV Epley
Arm Type
Experimental
Arm Description
Only Epley training.
Arm Title
BPPV Optocinetic
Arm Type
Experimental
Arm Description
Only Optocinetic training.
Intervention Type
Behavioral
Intervention Name(s)
Neurorehabilitation
Other Intervention Name(s)
BPPV group
Intervention Description
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.
Primary Outcome Measure Information:
Title
EQ5D-5L
Description
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.
Time Frame
5 weeks
Title
Beam Walking test
Description
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.
Time Frame
5 weeks
Title
Posturography
Description
Noninvasive intervention where static equilibrium is examined. The program determines the quality and frequency of the displacements.
Time Frame
5 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility 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
Facility Information:
Facility Name
Somogy Megyei Kaposi Mór Oktató Kórház
City
Kaposvár
State/Province
Somogy
ZIP/Postal Code
7400
Country
Hungary

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
https://www.ncbi.nlm.nih.gov/pubmed/?term=BPPV+rehabilitation
Description
BPPV rehabilitation

Learn more about this trial

Objective Examination and Rehabilitation Treatment of Patients With BPPV

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