Virtual Reality Compared to Other Forms of Optokinetic Stimulation in the Rehabilitation of Vestibular Syndromes. (EquiRV)
Primary Purpose
Vestibular Syndrome, Optokinetic Stimulation
Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Vestibular rehabilitation with virtual reality
Standard optokinetic stimulator or dynamic visual surround
Sponsored by
About this trial
This is an interventional treatment trial for Vestibular Syndrome focused on measuring virtual reality, vestibular, balance, rehabilitation
Eligibility Criteria
Inclusion Criteria:
- Symptomatology related to a vestibular disorder, eligible for a rehabilitation program Possible standing position
- Informed subject and having signed the informed consent form
- Major subject
- Affiliation to a social security scheme
Exclusion Criteria:
- Badly sighted or blind subject (sharpness <1 / 10th)
- Absence of vision of the reliefs
- Strabismus important
- History of epilepsy
- General state strongly altered
- Pregnant subject
- Major protected by law
- Subject deprived of liberty
Sites / Locations
- CH Paul Coste Floret/ Pavillon Jeanne d'Arc/ LeroyRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Virtual Reality Arm
Control Arm
Arm Description
Outcomes
Primary Outcome Measures
Balance score with eyes closed on an unstable plane during a sensory organization test
Realized with the Framiral® multitest equilibre. Framiral multitest equilibre is a posturography platform for performing vestibular assessments and targeted rehabilitation exercises
Secondary Outcome Measures
Others score of the sensory organization test
Realized with the Framiral® multitest equilibre.Framiral multitest equilibre is a posturography platform for performing vestibular assessments and targeted rehabilitation exercises
The Dizziness Handicap Inventory
The Dizziness Handicap Inventory
The Simulator Sickness Questionnaire
This questionnaire includes the following questions: "Not at all", "A little", "Moderately" and "Severely", each answer is worth 0, 1, 2 or 3 points. The total score is equal to 48, the two scores are calculable "Nausea" on 27 and "Oculomotor" on 21. The higher the score, the more the side effects are important.l 10 minutes
Full Information
NCT ID
NCT03838562
First Posted
January 28, 2019
Last Updated
March 4, 2023
Sponsor
University Hospital, Montpellier
1. Study Identification
Unique Protocol Identification Number
NCT03838562
Brief Title
Virtual Reality Compared to Other Forms of Optokinetic Stimulation in the Rehabilitation of Vestibular Syndromes.
Acronym
EquiRV
Official Title
Non-inferiority of Virtual Reality Compared to Other Forms of Optokinetic Stimulation in the Rehabilitation of Vestibular Syndromes. Randomized Controlled Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 23, 2019 (Actual)
Primary Completion Date
July 23, 2023 (Anticipated)
Study Completion Date
November 23, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Context and justification: Vertigo leads to medical consultation, interruption of daily activities or work stoppage in 80% of cases. Optokinetic stimulation is used in awareness and adaptation exercises. The technology of three-dimensional head-mounted provides a strong immersion allowing optokinetic stimulation but studies interested in virtual reality in the context of balance rehabilitation have not been able to highlight the superiority of this therapy. The investigators therefore propose a non-inferiority trial because of the affordable price and small size of three-dimensional head-mounted.
Objectives : The objective of this study is to evaluate whether a rehabilitation program using virtual reality is as effective as a reference program using Smart Equitest and an optokinetic stimulator to improve the balance of patients with vestibular syndrome after 3 or 4 weeks of rehabilitation.
The investigators also assess the disability related to vertigo and balance disorders as well as the tolerance of virtual reality Methodology: Prospective, randomized controlled non-inferiority trial, monocentric, 2 parallel arm, with blind assessed after 3 or 4 weeks of follow-up.
The inclusion criteria are the pathologies eligible for a vestibular rehabilitation program and the possible standing position.
The criteria for non-inclusion are visually impaired or blind subjects, lack of relief vision, history of epilepsy, significant strabismus, permanent bilateral vestibular areflexes and Ménière's disease.
The main evaluation criterion is the balance score obtained with eyes closed on an unstable plane during a sensory organization test performed on a dynamic posturology platform, obtained during the final evaluation.
The secondary judgment criteria are:
The balance scores obtained in the sensory organization test under other conditions.
The Dizziness Handicap Inventory obtained during the final evaluation and three months after the end of the program.
The tolerance of virtual reality will be measured weekly by the Simulator Sickness Questionnaire.
Statistics: The number of subjects to be included is 76, the analysis will first be performed per-protocol, the difference in scores between the two groups will be calculated, as well as its 95% confidence interval. If the lower bound of this interval is above the non-inferiority threshold, the same analysis will be performed on the population intending to treat (all randomized patients).
Process: Recruitment and rehabilitation take place at the CH Coste Floret. The duration of inclusions is 27 months, The duration of patient participation in the protocol is 4 months. Patients are cared for 21 or 28 days with two sessions of physiotherapy per day, five days a week, then resolved by telephone 3 months after the rehabilitation Feasibility: CH Coste Floret has the human and material resources necessary to carry out the protocol. The PMSI data show that the department receives about 40 patients per year who are likely to participate in the protocol.
Outcomes / perspectives: In the event of a result validating the non-inferiority of virtual reality, this study could provide further evidence of the value of this type of tool for the rehabilitation of subjects suffering from vestibular disorders. In addition, a medico-economic study would be possible in order to reinforce the advantages of virtual reality helmets.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vestibular Syndrome, Optokinetic Stimulation
Keywords
virtual reality, vestibular, balance, rehabilitation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
76 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Virtual Reality Arm
Arm Type
Experimental
Arm Title
Control Arm
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
Vestibular rehabilitation with virtual reality
Intervention Description
Both group follow three or four weeks of vestibular rehabilitation program with 2 sessions of physical therapy per day and one collective session of balance exercices per day, five day per week. More orthoptist care and muscle strengthening.
The exercises performed include rotating exercises, static balance exercises with eyes open and closed, head fixed and with head oscillation. Exercises on unstable planes and on dynamic force platforms. Different walking and eye stabilization exercises.
Only visual misinformation is distinct in both groups. Optokinetic application with three-dimensional head-mounted is used in the experimental group.
Intervention Type
Other
Intervention Name(s)
Standard optokinetic stimulator or dynamic visual surround
Intervention Description
Both group follow three or four weeks of vestibular rehabilitation program with 2 sessions of physical therapy per day and one collective session of balance exercices per day, five day per week. More orthoptist care and muscle strengthening.
The exercises performed include rotating exercises, static balance exercises with eyes open and closed, head fixed and with head oscillation. Exercises on unstable planes and on dynamic force platforms. Different walking and eye stabilization exercises.
Only visual misinformation is distinct in both groups. Standard optokinetic stimulator (stimulopt) or dynamic visual surround (smart equitest) are used in the control group.
Primary Outcome Measure Information:
Title
Balance score with eyes closed on an unstable plane during a sensory organization test
Description
Realized with the Framiral® multitest equilibre. Framiral multitest equilibre is a posturography platform for performing vestibular assessments and targeted rehabilitation exercises
Time Frame
after 3 or 4 weeks of rehabilitation
Secondary Outcome Measure Information:
Title
Others score of the sensory organization test
Description
Realized with the Framiral® multitest equilibre.Framiral multitest equilibre is a posturography platform for performing vestibular assessments and targeted rehabilitation exercises
Time Frame
3 or 4 weeks
Title
The Dizziness Handicap Inventory
Time Frame
3 or 4 weeks
Title
The Dizziness Handicap Inventory
Time Frame
4 month
Title
The Simulator Sickness Questionnaire
Description
This questionnaire includes the following questions: "Not at all", "A little", "Moderately" and "Severely", each answer is worth 0, 1, 2 or 3 points. The total score is equal to 48, the two scores are calculable "Nausea" on 27 and "Oculomotor" on 21. The higher the score, the more the side effects are important.l 10 minutes
Time Frame
weekly from week 1 to week 3 or 4
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Symptomatology related to a vestibular disorder, eligible for a rehabilitation program Possible standing position
Informed subject and having signed the informed consent form
Major subject
Affiliation to a social security scheme
Exclusion Criteria:
Badly sighted or blind subject (sharpness <1 / 10th)
Absence of vision of the reliefs
Strabismus important
History of epilepsy
General state strongly altered
Pregnant subject
Major protected by law
Subject deprived of liberty
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Isabelle LAFFONT, PUPH
Phone
0467338664
Email
i-laffont@chu-montpellier.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Gaël Le Perf
Phone
0651763239
Email
g.leperf@hopital-lamalou.fr
Facility Information:
Facility Name
CH Paul Coste Floret/ Pavillon Jeanne d'Arc/ Leroy
City
Lamalou-les-Bains
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gaël LE PERF
Phone
0651763239
Email
leperf@hopital-lamalou.fr
First Name & Middle Initial & Last Name & Degree
Gaël LE PERF
12. IPD Sharing Statement
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Virtual Reality Compared to Other Forms of Optokinetic Stimulation in the Rehabilitation of Vestibular Syndromes.
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