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Testing an Intraoral Electronic Balance Aid for Vestibular Imbalance

Primary Purpose

Vestibular Disorder

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
EquiCue (Intraoral Electronic Balance Aid)
Sponsored by
Innervo Technology LLC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Vestibular Disorder focused on measuring Bilateral Vestibular Hypofunction, Unilateral Vestibular Hypofunction, Imbalance

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. English speaking adults with ages between 18-85.
  2. Patients with imbalance resulted from vestibular loss or vestibulopathy.
  3. Priority given to those who took vestibular rehabilitation therapy but without satisfactory improvement.

Exclusion Criteria:

  1. Inability to follow instructions.
  2. Any visible abnormalities on the hard palate that prevent use of the palatal device.
  3. Any mental or physical illness beyond the secondary effects of vestibular loss that prevent recognition or effective use of the alternative feedback.

Sites / Locations

  • MU ENT Hearing and Balance Center
  • Blue Ridge Physical Therapy

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Vestibular Patients for EquiCue Testing

Arm Description

Subjects with vestibular deficiency will try the intraoral electronic balance aid to see whether there is improvement in balance.

Outcomes

Primary Outcome Measures

Equilibrium Score
Equilibrium scores for each trial for each condition from Sensory Organization Test (EquiTest). Conditions: 1-6; with or without using EquiCue intraoral balance aid. Equilibrium scores were generated from the EquiTest CDP (computerized dynamic posturography) platform to assess standing balance of a patient ranging from 0 (all falls) to 100 (perfect balance with no sway), with higher scores indicating better balance performance. An equilibrium score of 70 and above is considered normal.

Secondary Outcome Measures

Perceived Intensity Level
The perceived Intensity level (from 0 to 5) as judged by a patient in response to pulsed stimuli applied on the palatal surface after adjustment of device settings for that patient. 1 - barely perceptible, 2 - weak, 3 - good, 4 - strong, 5 - painful.
Dynamic Gait Index
A subject's gait is evaluated by a physical therapist when no device is worn and when alternative sensory feedback of head movement is presented to the patient using the device. 7 walking exercises were administrated for each DGI test, with a score in the range of 0 - 3 (0 for severely impaired and 3 for normal gait) for each exercise, and a total score in the range of 0 - 21 for each test.
Analog Visual Scale for the Perceived Frequency of Stimulation Pulses
A patient's assessment of the speed of pulses to quantify perceptual difference in the pulse frequencies of the feedback on the palatal surface.

Full Information

First Posted
March 30, 2016
Last Updated
April 4, 2019
Sponsor
Innervo Technology LLC
Collaborators
University of Missouri-Columbia, Blue Ridge Physical Therapy
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1. Study Identification

Unique Protocol Identification Number
NCT02735096
Brief Title
Testing an Intraoral Electronic Balance Aid for Vestibular Imbalance
Official Title
Palatal Device Providing In-situ Sensory Feedback for Patients With Vestibular Imbalance
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Terminated
Why Stopped
Funding ended at the end of 2016
Study Start Date
July 2016 (undefined)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
October 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Innervo Technology LLC
Collaborators
University of Missouri-Columbia, Blue Ridge Physical Therapy

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The human body uses vestibular feedback in coordination with visual and somatosensory information to maintain balance and posture. However, various inner-ear disorders due to aging, drug toxicity, viral infections, and injury, etc., may result in loss of vestibular feedback, which makes it difficult for an individual to maintain balance. This study investigates the use of a hidden and noninvasive balance device EquiCue™ V1 developed by Innervo Technology for vestibular substitution. EquiCue™ V1 is a retainer-like intraoral electronic balance aid entirely worn inside the oral cavity and provides in-situ sensory feedback of head tilting and motion on the roof of the mouth. The feedback is delivered by applying small and controlled electrical pulses at precise locations on the palatal surface according to an encoded pattern. This pilot study is to determine how this alternative sensory feedback on the roof of the mouth can be used to improve balance for patients with vestibular loss.
Detailed Description
Background Vestibular imbalance is prevalent in the United States and around the world. According to NIDCD, 4% (8 million) of American adults report a chronic problem with balance (visit vestibular.org for more information). The leading cause of imbalance is vestibular dysfunction. Various vestibular disorders due to aging, diseases, ototoxicity, and injuries, etc. can cause damage or degradation of the vestibular system, resulting in loss of vestibular feedback. Symptoms associated with vestibular loss include: difficulty maintaining straight posture; stumbling or unable to walk straight; lose balance on uneven surfaces or under dim lighting; floating sensation and tendency to look downward to confirm the location of the ground. Vestibular imbalance greatly increases risk of falling and has such disabling effects ranging from reduced activity levels to total loss of mobility. Vestibular rehabilitation therapies (VRT) may help vestibular patients to compensate with vision and proprioception. However, such compensation is not adequate because the brain often needs a reliable reference in order to use visual and somatosensory information for perception of self-motion and spatial orientation. Consequently, many patients with vestibular imbalance fail to compensate, especially those with profound vestibular loss. Even those who respond to VRT may experience constant physical and mental stress due to overreliance on vision and proprioception that can be misleading in busy environments. EquiCue™ Intraoral Balance Aid The intraoral balance aid EquiCue™ V1 is a hidden and noninvasive balance device that vestibular patients can use in various indoor and outdoor activities. It is a retainer-like device entirely worn inside the oral cavity, with no need of surgical implantation, and can be removed when not in use. The device provides in-situ sensory feedback of head tilt and motion by applying small electrical pulses on the roof of the mouth. By sensing the feedback from the device, an individual with vestibular loss can have better judgment of the tilt and motion of the head and make physical adjustment accordingly for better balance of the body. Since the device does not cause alteration to the appearance of the user, patients may use it in public places such as shopping malls, supermarkets, and metro stations, while offering balance assistance and improved postural stability and gait in these busy environments. Human Subject Study The current study is an initial stage of a clinical trial on the use of EquiCue™ for patients with vestibular imbalance. The hypothesis is that EquiCue™ can at least partially substitute the lost vestibular function and therefore helps a vestibular patient to achieve better postural stability in daily activities. The basic questions regarding the technology are: 1) How to represent head movement using electrical pulses on the palate; 2) Whether the electrotactile presentation on the palate can be reliably recognized and used for balance control. The study also helps to understand the role of multisensory integration on balance, especially the impact of alternative sensory feedback on the balance system. Subjects participating in the study will be expected to wear a custom-made retainer-like device and perform movements to test their balance. If a patient is determined to be a suitable subject, the sensitivity profile on the palate of the patient will be measured. After an EquiCue™ intraoral device is custom made, the patient will be asked to fit the device inside the mouth, and verify the basic functionality of the device by identifying direction, perceived intensity, and sensory characteristics of stimuli from the device. The subject will then go through 3-4 sessions of training and testing in which the subject tries to associate the feedback with head movement and to integrate the feedback with other senses to achieve a better spatial orientation and balance. The improvement in balance and gait with the device will be evaluated by using standard tests on balance platforms (Computerized Dynamic Posturography) and Dynamic Gait Index. Tests will be made without wearing the device at the beginning and wearing the device at the end of each training session.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vestibular Disorder
Keywords
Bilateral Vestibular Hypofunction, Unilateral Vestibular Hypofunction, Imbalance

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
4 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vestibular Patients for EquiCue Testing
Arm Type
Experimental
Arm Description
Subjects with vestibular deficiency will try the intraoral electronic balance aid to see whether there is improvement in balance.
Intervention Type
Device
Intervention Name(s)
EquiCue (Intraoral Electronic Balance Aid)
Other Intervention Name(s)
EquiCue
Intervention Description
When the device is worn, a subject will receive small electrical pulses on roof of the mouth as alternative feedback of head tilting or movement.
Primary Outcome Measure Information:
Title
Equilibrium Score
Description
Equilibrium scores for each trial for each condition from Sensory Organization Test (EquiTest). Conditions: 1-6; with or without using EquiCue intraoral balance aid. Equilibrium scores were generated from the EquiTest CDP (computerized dynamic posturography) platform to assess standing balance of a patient ranging from 0 (all falls) to 100 (perfect balance with no sway), with higher scores indicating better balance performance. An equilibrium score of 70 and above is considered normal.
Time Frame
July 2016 - October 2016 (~ 4 months)
Secondary Outcome Measure Information:
Title
Perceived Intensity Level
Description
The perceived Intensity level (from 0 to 5) as judged by a patient in response to pulsed stimuli applied on the palatal surface after adjustment of device settings for that patient. 1 - barely perceptible, 2 - weak, 3 - good, 4 - strong, 5 - painful.
Time Frame
July 2016 - October 2016 (~ 4 months)
Title
Dynamic Gait Index
Description
A subject's gait is evaluated by a physical therapist when no device is worn and when alternative sensory feedback of head movement is presented to the patient using the device. 7 walking exercises were administrated for each DGI test, with a score in the range of 0 - 3 (0 for severely impaired and 3 for normal gait) for each exercise, and a total score in the range of 0 - 21 for each test.
Time Frame
July 2016 - October 2016 (~ 4 months)
Title
Analog Visual Scale for the Perceived Frequency of Stimulation Pulses
Description
A patient's assessment of the speed of pulses to quantify perceptual difference in the pulse frequencies of the feedback on the palatal surface.
Time Frame
July 2016 - October 2016 (~ 4 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: English speaking adults with ages between 18-85. Patients with imbalance resulted from vestibular loss or vestibulopathy. Priority given to those who took vestibular rehabilitation therapy but without satisfactory improvement. Exclusion Criteria: Inability to follow instructions. Any visible abnormalities on the hard palate that prevent use of the palatal device. Any mental or physical illness beyond the secondary effects of vestibular loss that prevent recognition or effective use of the alternative feedback.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hui Tang, Ph.D
Organizational Affiliation
Innervo Technology LLC
Official's Role
Study Director
Facility Information:
Facility Name
MU ENT Hearing and Balance Center
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65201
Country
United States
Facility Name
Blue Ridge Physical Therapy
City
Independence
State/Province
Missouri
ZIP/Postal Code
64055
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Participants' age and history of illness (i.e., vestibular loss) will be shared. However, no personal identifiable information will be collected and shared.
Citations:
PubMed Identifier
16562639
Citation
Tang H, Beebe DJ. An oral tactile interface for blind navigation. IEEE Trans Neural Syst Rehabil Eng. 2006 Mar;14(1):116-23. doi: 10.1109/TNSRE.2005.862696.
Results Reference
background
Citation
Tang H; Beebe DJ. Design and microfabrication of a flexible oral electrotactile display. Journal of Microelectromechanical Systems. 2003 Feb;12(1):29-36.
Results Reference
background
PubMed Identifier
18413905
Citation
Danilov YP, Tyler ME, Skinner KL, Hogle RA, Bach-y-Rita P. Efficacy of electrotactile vestibular substitution in patients with peripheral and central vestibular loss. J Vestib Res. 2007;17(2-3):119-30.
Results Reference
background
PubMed Identifier
17021893
Citation
Dozza M, Horak FB, Chiari L. Auditory biofeedback substitutes for loss of sensory information in maintaining stance. Exp Brain Res. 2007 Mar;178(1):37-48. doi: 10.1007/s00221-006-0709-y. Epub 2006 Oct 5.
Results Reference
background
PubMed Identifier
12867668
Citation
Wall C 3rd, Merfeld DM, Rauch SD, Black FO. Vestibular prostheses: the engineering and biomedical issues. J Vestib Res. 2002-2003;12(2-3):95-113.
Results Reference
background
PubMed Identifier
11801950
Citation
Brown KE, Whitney SL, Wrisley DM, Furman JM. Physical therapy outcomes for persons with bilateral vestibular loss. Laryngoscope. 2001 Oct;111(10):1812-7. doi: 10.1097/00005537-200110000-00027.
Results Reference
background
PubMed Identifier
19468085
Citation
Agrawal Y, Carey JP, Della Santina CC, Schubert MC, Minor LB. Disorders of balance and vestibular function in US adults: data from the National Health and Nutrition Examination Survey, 2001-2004. Arch Intern Med. 2009 May 25;169(10):938-44. doi: 10.1001/archinternmed.2009.66. Erratum In: Arch Intern Med. 2009 Aug 10;169(15):1419.
Results Reference
background
Links:
URL
https://vestibular.org/sites/default/files/page_files/Vestibular%20Disorders%20an%20Overview.pdf
Description
Vestibular Disorder-Overview
URL
https://vestibular.org/sites/default/files/page_files/Human%20Balance%20System.pdf
Description
The Human Balance System

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Testing an Intraoral Electronic Balance Aid for Vestibular Imbalance

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