Vestibular AbnormalityNCT03251586
Test-Retest Reliability of oVEMP's Across Different Electrode Montages
A study testing oVEMP - infra-orbital electrode montage and oVEMP - belly-tendon electrode montage in people with Vestibular Abnormality and Vestibular Nerve Disorders, run by Vanderbilt University Medical Center at 1 site in United States.
Trial summary
"Test-Retest Reliability of ocular vestibular evoked myogenic potentials (oVEMPs) across different electrode montages." The purpose of this project is to compare the response characteristics of the ocular vestibular evoked myogenic potential in patients grouped by decade (i.e. Read more about this study
- Who is it for?
- Ages 20 to 99 yearsHealthy volunteers can take part
- Conditions the study is for
- Vestibular Abnormality, Vestibular Nerve Disorders
- What is being tested?
- oVEMP - infra-orbital electrode montage and oVEMP - belly-tendon electrode montage
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 0 participants
- Where
- 1 siteUnited States
- Study dates
- Apr 2018to May 2018
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 to 99 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Normal hearing and no history of balance disorders
Who cannot join
- Hearing loss, a large amount of ear wax, inner ear of balance problems, and/or no recordable eye muscle responses
Trial locations and contacts
1 site in 1 country.
United States1 site
Vanderbilt University Medical Center
Nashville, Tennessee, 37232
About this study
"Test-Retest Reliability of ocular vestibular evoked myogenic potentials (oVEMPs) across different electrode montages."
The purpose of this project is to compare the response characteristics of the ocular vestibular evoked myogenic potential in patients grouped by decade (i.e. 20's-90's) using two different recording montages and two different stimulus types (i.e. air and bone conducted sound). The long-term goal is to increase the sensitivity and specificity of the oVEMP when used clinically to identify vestibular disorders affecting the utricle and superior portion of the vestibular nerve.
.
Read the detailed description
Specific Aim: Compare the difference in the contralateral peak-to-peak N1-P1 amplitude and N1 latency between the belly tendon electrode montage with the conventional infraorbital electrode montage in otologically normal patients grouped by decade with the goal of developing normative values to use clinically.
The oVEMP is a short latency (~10 ms), negative polarity evoked myogenic potential that is recorded from the extraocular muscles. The oVEMP test is well-tolerated by patients and is simple to administer. Whereas the recording of the cVEMP to air-conducted stimuli represents a means for evaluating the function of the saccule and inferior vestibular nerve, the oVEMP in response to mechanical, and probably air conducted stimuli, is now felt to represent a method for assessing the functional integrity of the utricle and superior vestibular nerve.
The oVEMP response is recorded from beneath both the ipsilateral and contralateral eyes, but the largest response is typically seen in the contralateral recording. The contralateral utricular-ocular pathway terminates on the inferior oblique muscle, the electrical field of which can be recorded by an electrode placed at the midline of the lower lid and having the subject gaze upward (i.e. which results in the inferior oblique muscle becoming more superficial to the location of the surface electrode.
The the absolute oVEMP N1 peak-to-peak amplitude has become the most important measurement for diagnostic purposes. Typical oVEMP latencies are ~11 ms for the negative peak (N1) and ~15 ms for the following positive peak (P1) .
Variables that may confound recording oVEMPs include body position and electrode montages. Regarding electrode placement, there are three different electrode montages that have been studied and implemented clinically. The vast majority of clinics favor the electrode montage reported in the early papers describing the oVEMP. The authors reported that the non-inverting electrode was placed infraorbitally at the margin of the lower eyelid. The inverting electrode was placed 2 cm inferior to the location of the non-inverting electrode. Two additional electrode montages that have been reported include: 1) the noninverting electrodes placed at the margin of the lower eyelid slightly lateral to midline and the inverting electrode placed rostral to the inner canthus of the eye, and, 2) the noninverting electrodes placed at the middle of the lmargin of the lower eyelid and a single common inverting electrode placed on the chin. A report by Sandhu et al. (2013) indicated that the maximal oVEMP amplitude was recorded with the former electrode montage. In this montage, the inverting electrode is placed over a tendon, which is believed to be (relatively) electrically neutral.
Skin surface electrodes are sensitive to the desired muscle activity (i.e. signal) recorded locally as well as non-stimulus-related electrical activity (i.e. noise) that can be both endogenous and exogenous. Where the signal is common to both the inverting and non-inverting electrodes this activity routed into a differential electrode can result in cancellation of some or all of the desired signal.
Recently published data from our laboratory has shown that the Sandhu montage (i.e. the "belly-tendon electrode montage) in the sitting position is the optimal method for testing patients who are otologically and neurologically normal. This montage is associated with a larger N1 amplitude and a larger peak-to-peak amplitude for oVEMP measurements for young, normal patients. Due to the knowledge that the amplitude of the oVEMP response decreases with age, however, normative values based on decade would be necessary to have the oVEMP response be as clinically useful as possible.
Significance and Potential of the Research:
Establishing normative values based on decade will allow for higher sensitivity and specificity to vestibular impairments affecting the utricle and superior portion of the vestibular nerve, as well as increase the sensitivity and specificity to disorders such as Superior Semicircular Canal Dehiscence Syndrome.
Methods:
Subjects: Participants will include groups of patients between 20-90 years of age. The groups will be composed of 10-15 subjects per group to allow for normative data to be calculated. Participants will be recruited by phone using databases housed in the Odess Otolaryngology Department at Vanderbilt Bill Wilkerson Center, via flyers posted at Vanderbilt University Medical Center, and through Research Match email blasts. The study protocol will undergo review by the Vanderbilt Institutional Review Board (submitted-see Appendix).
oVEMP Recording: For the oVEMP recording (utricular assessment), subjects will be seated in a comfortable reclining will be compared during this study. First, an electrode montage and recording parameters similar to those reported by Chihara et al. (2007) will be used to record the oVEMP. Disposable silver/silverchloride electrodes will be placed infraorbitally beneath each eye (i.e., infraorbital 1 cm) representing the non-inverting amplifier inputs and 3cm infraorbitally will serve as the location for the inverting electrode. A second electrode montage with recording parameters similar those reported by Sandhu et al. (2013) will be used simultaneously to record oVEMP responses. Disposable silver/silverchloride electrodes will be placed on the belly of the inferior oblique muscle representing the non-inverting amplifier inputs and the tendon of the inferior oblique muscle will serve as the location for the inverting electrode. The ground electrode will be placed at Fpz for both electrode montages.
When recording the oVEMP, the subjects will be seated and instructed to keep their head at midline and gaze at a target positioned ~30° upward at midline. During the recording, the investigator will monitor to ensure the subject's chin is parallel to the horizon. Stimuli for the oVEMP recordings will be presented monaurally through Etymotic ER-3A insert earphones or a B81 bone conductor and consist of 500 Hz tone bursts presented at a rate of 5.1/sec. The tone burst will have a 2 cycle rise time, 1 cycle plateau and a 2 cycle fall time. A Neuroscan (Herndon, UA) multi-channel evoked potential recording system will enable us to record simultaneously the oVEMP response from each of the two electrode montages. EMG activity will be amplified by 100,000 times and signal averaged over 100 msec. A minimum of 120 individual samples will be collected for each recording. Each tracing will be replicated at least one time so that the waveform reproducibility can be estimated. Order effects will be eliminated by counterbalancing the order of the starting ear. oVEMPs from the two electrode montages will be recorded simultaneously, so counterbalancing the electrode montage will be unnecessary. A minimum of two amplitude measures will be completed for each electrode montage condition in each position, for a total minimum of 8 recordings per subject. The subject will be given 1-2 minutes to rest their eyes between recordings.
Stimulus level will be calibrated in dBpeak SPL using a 2-cm3 coupler to a sound-level meter (Bruel \& Kjaer). The stimulus waveforms and amplitude spectra will be measured by routing the air conduction output of the sound-level meter to a spectrum analyzer.
Statistical Methods:
Analysis: Summary statistics will be provided for all demographic and clinical variables, along with 95% confidence intervals and side-by-side boxplots. Between-group differences in categorical variables will be assessed via chi-squared tests while differences in continuous variables will be assessed via the Wilcoxin rank-sum test (using significance level alpha = 0.0125 in primary analysis as per the power calculation above). Hotelling's T-squared distribution will also be used as an omnibus or simultaneous test that the groups are the same for all variables in the primary analysis. Amplitude differences obtained using each montage will be calculated as a change expressed in percentage using the formula below:
(n1-p1 amplitude montage2 - n1-p1 amplitude montage 1)
--------------------------------------------------------------- n1-p1 amplitude montage 1
All statistical analyses will be performed with SPSS 23.
Facilities Available: The Vanderbilt Balance Disorders Laboratory is located in the Bill Wilkerson Center. The Balance Disorders Laboratory is equipped with state-of-the art equipment for comprehensive assessment of vestibular and auditory disorders. The facility includes a sound treated room, five diagnostic audiometers, five compact disk players for speech audiometry, five immittance meters, three otoacoustic emissions devices, two rotary vestibular test chairs, three videonystagmography systems, a computerized electronystagmography system, a computerized dynamic posturography system, a Neuroscan evoked response system with capability for 64 channel simultaneous brain signal acquisition, and 4 2-channel clinical evoked potentials systems.
- Conditions
- Vestibular Abnormality, Vestibular Nerve Disorders
- Being tested
- oVEMP - infra-orbital electrode montage, oVEMP - belly-tendon electrode montage
- Medical subject headings
- Vestibulocochlear Nerve Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
oVEMP - infra-orbital electrode montageDiagnostic test
oVEMPs are short latency (~10 ms) stimulus-synchronized extra-ocular muscle reflexes produced in response to appropriate stimuli. The response is believed to originate from excitation of the utricular macula with the subsequent neural response relayed to the brain by the superior portion of the vestibular nerve. Changes in the electrical field of the contralateral inferior oblique muscle can be recorded by an electrode placed at the infra-ocular midline of the lower lid while having the subject gaze upward. The conventional electrode montage, the infra-orbital electrode montage, has the active electrode placed directly inferior to the eye and the reference electrode placed 2-3 cm below the active on the cheek. This electrode montage may result in reference contamination, which will cause an artificially reduced amplitude response, as a portion of the response can be measured by the reference electrode.
oVEMP - belly-tendon electrode montageDiagnostic test
oVEMPs are short latency (~10 ms) stimulus-synchronized extra-ocular muscle reflexes produced in response to appropriate stimuli. The response is believed to originate from excitation of the utricular macula with the subsequent neural response relayed to the brain by the superior portion of the vestibular nerve. Changes in the electrical field of the contralateral inferior oblique muscle can be recorded by an electrode placed at the infra-ocular midline of the lower lid while having the subject gaze upward. The belly-tendon electrode montage consists of an active electrode placed laterally to the midline of the lower eyelid and a reference electrode placed on the inner canthus. This reference location is believed to be electrically neutral, and should therefore result in larger amplitude responses as the response would not be subject to reference contamination.
| Study group | Role | What they receive |
|---|---|---|
| 20-29 | Experimental | Participants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. Receives: Diagnostic Test: oVEMP - infra-orbital electrode montage; Diagnostic Test: oVEMP - belly-tendon electrode montage |
| 30-39 | Experimental | Participants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. Receives: Diagnostic Test: oVEMP - infra-orbital electrode montage; Diagnostic Test: oVEMP - belly-tendon electrode montage |
| 40-49 | Experimental | Participants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. Receives: Diagnostic Test: oVEMP - infra-orbital electrode montage; Diagnostic Test: oVEMP - belly-tendon electrode montage |
| 50-59 | Experimental | Participants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. Receives: Diagnostic Test: oVEMP - infra-orbital electrode montage; Diagnostic Test: oVEMP - belly-tendon electrode montage |
| 60-69 | Experimental | Participants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. Receives: Diagnostic Test: oVEMP - infra-orbital electrode montage; Diagnostic Test: oVEMP - belly-tendon electrode montage |
| 70-79 | Experimental | Participants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. Receives: Diagnostic Test: oVEMP - infra-orbital electrode montage; Diagnostic Test: oVEMP - belly-tendon electrode montage |
| 80-89 | Experimental | Participants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. Receives: Diagnostic Test: oVEMP - infra-orbital electrode montage; Diagnostic Test: oVEMP - belly-tendon electrode montage |
| 90-99 | Experimental | Participants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. Receives: Diagnostic Test: oVEMP - infra-orbital electrode montage; Diagnostic Test: oVEMP - belly-tendon electrode montage |
What is being measured
The primary outcome is the main question the study is designed to answer.
Development of Normative Values per Decade
The oVEMP N1-P1 amplitude and N1 latency will be measured for each subject and will be used to calculate normative values for each decade. The goal is to provide clinics with normative information to base clinical evaluations on.
Measured: 5 months for data collection, one visit per subject.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Aug 2017
- Study startApr 2018 (estimated)
- Primary completionApr 2018 (estimated)
- Study completionMay 2018 (estimated)
Why it stopped: Due to time constraints, the study will not be able to be completed as outlined
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (14)Papers the sponsor has linked to this study.
- Other trials for Vestibular AbnormalityStudies of the same condition, open and under way.
- More trials run by Vanderbilt University Medical CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Vanderbilt University Medical Center
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Kathryn Makowiec, Vanderbilt University Medical Center
- Investigators
- Kathryn F Makowiec, AuD, Principal investigator, Vanderbilt University Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03251586
- Sponsor's protocol ID
- 140805
- Status last verified
- Mar 2018
- First submitted
- 11 Aug 2017
- Last updated
- 15 Mar 2018
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- No: There is no plan to share IPD with other researchers.
Publications
Chang CM, Cheng PW, Wang SJ, Young YH. Effects of repetition rate of bone-conducted vibration on ocular and cervical vestibular-evoked myogenic potentials. Clin Neurophysiol. 2010 Dec;121(12):2121-7. doi: 10.1016/j.clinph.2010.05.013. Epub 2010 Jun 11.
PubMed 20541460Chihara Y, Iwasaki S, Ushio M, Murofushi T. Vestibular-evoked extraocular potentials by air-conducted sound: another clinical test for vestibular function. Clin Neurophysiol. 2007 Dec;118(12):2745-51. doi: 10.1016/j.clinph.2007.08.005. Epub 2007 Oct 1.
PubMed 17905655Curthoys IS, Iwasaki S, Chihara Y, Ushio M, McGarvie LA, Burgess AM. The ocular vestibular-evoked myogenic potential to air-conducted sound; probable superior vestibular nerve origin. Clin Neurophysiol. 2011 Mar;122(3):611-616. doi: 10.1016/j.clinph.2010.07.018. Epub 2010 Aug 14.
PubMed 20709596Govender S, Rosengren SM, Colebatch JG. The effect of gaze direction on the ocular vestibular evoked myogenic potential produced by air-conducted sound. Clin Neurophysiol. 2009 Jul;120(7):1386-91. doi: 10.1016/j.clinph.2009.04.017. Epub 2009 May 22.
PubMed 19464947Makowiec K, McCaslin DL, Jacobson GP, Hatton K, Lee J. Effect of Electrode Montage and Head Position on Air-Conducted Ocular Vestibular Evoked Myogenic Potential. Am J Audiol. 2017 Jun 13;26(2):180-188. doi: 10.1044/2017_AJA-16-0108.
PubMed 28520834Kantner C, Gurkov R. Characteristics and clinical applications of ocular vestibular evoked myogenic potentials. Hear Res. 2012 Dec;294(1-2):55-63. doi: 10.1016/j.heares.2012.10.008. Epub 2012 Oct 30.
PubMed 23123220Murnane OD, Akin FW, Kelly KJ, Byrd S. Effects of stimulus and recording parameters on the air conduction ocular vestibular evoked myogenic potential. J Am Acad Audiol. 2011 Jul-Aug;22(7):469-80. doi: 10.3766/jaaa.22.7.7.
PubMed 21993052Nguyen KD, Welgampola MS, Carey JP. Test-retest reliability and age-related characteristics of the ocular and cervical vestibular evoked myogenic potential tests. Otol Neurotol. 2010 Jul;31(5):793-802. doi: 10.1097/MAO.0b013e3181e3d60e.
PubMed 20517167Piker EG, Jacobson GP, McCaslin DL, Hood LJ. Normal characteristics of the ocular vestibular evoked myogenic potential. J Am Acad Audiol. 2011 Apr;22(4):222-30. doi: 10.3766/jaaa.22.4.5.
PubMed 21586257Piker EG, Jacobson GP, Burkard RF, McCaslin DL, Hood LJ. Effects of age on the tuning of the cVEMP and oVEMP. Ear Hear. 2013 Nov-Dec;34(6):e65-73. doi: 10.1097/AUD.0b013e31828fc9f2.
PubMed 23673615Rosengren SM, McAngus Todd NP, Colebatch JG. Vestibular-evoked extraocular potentials produced by stimulation with bone-conducted sound. Clin Neurophysiol. 2005 Aug;116(8):1938-48. doi: 10.1016/j.clinph.2005.03.019.
PubMed 15979939Sandhu JS, George SR, Rea PA. The effect of electrode positioning on the ocular vestibular evoked myogenic potential to air-conducted sound. Clin Neurophysiol. 2013 Jun;124(6):1232-6. doi: 10.1016/j.clinph.2012.11.019. Epub 2013 Jan 18.
PubMed 23333609Todd NP, Rosengren SM, Aw ST, Colebatch JG. Ocular vestibular evoked myogenic potentials (OVEMPs) produced by air- and bone-conducted sound. Clin Neurophysiol. 2007 Feb;118(2):381-90. doi: 10.1016/j.clinph.2006.09.025. Epub 2006 Dec 1.
PubMed 17141563Welgampola MS, Carey JP. Waiting for the evidence: VEMP testing and the ability to differentiate utricular versus saccular function. Otolaryngol Head Neck Surg. 2010 Aug;143(2):281-3. doi: 10.1016/j.otohns.2010.05.024.
PubMed 20647135
Study at a glance
From the registry record, last updated by the sponsor on 15 Mar 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Test-Retest Reliability of oVEMP's Across Different Electrode Montages
- ClinicalTrials.gov ID
- NCT03251586
- Acronym / sponsor ID
- 140805
- Conditions
- Vestibular Abnormality, Vestibular Nerve Disorders
- Study type
- Interventional
- Recruitment status
- WithdrawnReason stopped: Due to time constraints, the study will not be able to be completed as outlined
- Enrolment
- 0 participants (actual)
- Lead sponsor
- Vanderbilt University Medical CenterUniversity, hospital or other
- Study start
- Apr 2018 (estimated)
- Primary completion
- Apr 2018 (estimated)
- Study completion
- May 2018 (estimated)
- First posted
- 16 Aug 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
"Test-Retest Reliability of ocular vestibular evoked myogenic potentials (oVEMPs) across different electrode montages."
The purpose of this project is to compare the response characteristics of the ocular vestibular evoked myogenic potential in patients grouped by decade (i.e. 20's-90's) using two different recording montages and two different stimulus types (i.e. air and bone conducted sound). The long-term goal is to increase the sensitivity and specificity of the oVEMP when used clinically to identify vestibular disorders affecting the utricle and superior portion of the vestibular nerve.
.
Detailed description
Specific Aim: Compare the difference in the contralateral peak-to-peak N1-P1 amplitude and N1 latency between the belly tendon electrode montage with the conventional infraorbital electrode montage in otologically normal patients grouped by decade with the goal of developing normative values to use clinically.
The oVEMP is a short latency (~10 ms), negative polarity evoked myogenic potential that is recorded from the extraocular muscles. The oVEMP test is well-tolerated by patients and is simple to administer. Whereas the recording of the cVEMP to air-conducted stimuli represents a means for evaluating the function of the saccule and inferior vestibular nerve, the oVEMP in response to mechanical, and probably air conducted stimuli, is now felt to represent a method for assessing the functional integrity of the utricle and superior vestibular nerve.
The oVEMP response is recorded from beneath both the ipsilateral and contralateral eyes, but the largest response is typically seen in the contralateral recording. The contralateral utricular-ocular pathway terminates on the inferior oblique muscle, the electrical field of which can be recorded by an electrode placed at the midline of the lower lid and having the subject gaze upward (i.e. which results in the inferior oblique muscle becoming more superficial to the location of the surface electrode.
The the absolute oVEMP N1 peak-to-peak amplitude has become the most important measurement for diagnostic purposes. Typical oVEMP latencies are ~11 ms for the negative peak (N1) and ~15 ms for the following positive peak (P1) .
Variables that may confound recording oVEMPs include body position and electrode montages. Regarding electrode placement, there are three different electrode montages that have been studied and implemented clinically. The vast majority of clinics favor the electrode montage reported in the early papers describing the oVEMP. The authors reported that the non-inverting electrode was placed infraorbitally at the margin of the lower eyelid. The inverting electrode was placed 2 cm inferior to the location of the non-inverting electrode. Two additional electrode montages that have been reported include: 1) the noninverting electrodes placed at the margin of the lower eyelid slightly lateral to midline and the inverting electrode placed rostral to the inner canthus of the eye, and, 2) the noninverting electrodes placed at the middle of the lmargin of the lower eyelid and a single common inverting electrode placed on the chin. A report by Sandhu et al. (2013) indicated that the maximal oVEMP amplitude was recorded with the former electrode montage. In this montage, the inverting electrode is placed over a tendon, which is believed to be (relatively) electrically neutral.
Skin surface electrodes are sensitive to the desired muscle activity (i.e. signal) recorded locally as well as non-stimulus-related electrical activity (i.e. noise) that can be both endogenous and exogenous. Where the signal is common to both the inverting and non-inverting electrodes this activity routed into a differential electrode can result in cancellation of some or all of the desired signal.
Recently published data from our laboratory has shown that the Sandhu montage (i.e. the "belly-tendon electrode montage) in the sitting position is the optimal method for testing patients who are otologically and neurologically normal. This montage is associated with a larger N1 amplitude and a larger peak-to-peak amplitude for oVEMP measurements for young, normal patients. Due to the knowledge that the amplitude of the oVEMP response decreases with age, however, normative values based on decade would be necessary to have the oVEMP response be as clinically useful as possible.
Significance and Potential of the Research:
Establishing normative values based on decade will allow for higher sensitivity and specificity to vestibular impairments affecting the utricle and superior portion of the vestibular nerve, as well as increase the sensitivity and specificity to disorders such as Superior Semicircular Canal Dehiscence Syndrome.
Methods:
Subjects: Participants will include groups of patients between 20-90 years of age. The groups will be composed of 10-15 subjects per group to allow for normative data to be calculated. Participants will be recruited by phone using databases housed in the Odess Otolaryngology Department at Vanderbilt Bill Wilkerson Center, via flyers posted at Vanderbilt University Medical Center, and through Research Match email blasts. The study protocol will undergo review by the Vanderbilt Institutional Review Board (submitted-see Appendix).
oVEMP Recording: For the oVEMP recording (utricular assessment), subjects will be seated in a comfortable reclining will be compared during this study. First, an electrode montage and recording parameters similar to those reported by Chihara et al. (2007) will be used to record the oVEMP. Disposable silver/silverchloride electrodes will be placed infraorbitally beneath each eye (i.e., infraorbital 1 cm) representing the non-inverting amplifier inputs and 3cm infraorbitally will serve as the location for the inverting electrode. A second electrode montage with recording parameters similar those reported by Sandhu et al. (2013) will be used simultaneously to record oVEMP responses. Disposable silver/silverchloride electrodes will be placed on the belly of the inferior oblique muscle representing the non-inverting amplifier inputs and the tendon of the inferior oblique muscle will serve as the location for the inverting electrode. The ground electrode will be placed at Fpz for both electrode montages.
When recording the oVEMP, the subjects will be seated and instructed to keep their head at midline and gaze at a target positioned ~30° upward at midline. During the recording, the investigator will monitor to ensure the subject's chin is parallel to the horizon. Stimuli for the oVEMP recordings will be presented monaurally through Etymotic ER-3A insert earphones or a B81 bone conductor and consist of 500 Hz tone bursts presented at a rate of 5.1/sec. The tone burst will have a 2 cycle rise time, 1 cycle plateau and a 2 cycle fall time. A Neuroscan (Herndon, UA) multi-channel evoked potential recording system will enable us to record simultaneously the oVEMP response from each of the two electrode montages. EMG activity will be amplified by 100,000 times and signal averaged over 100 msec. A minimum of 120 individual samples will be collected for each recording. Each tracing will be replicated at least one time so that the waveform reproducibility can be estimated. Order effects will be eliminated by counterbalancing the order of the starting ear. oVEMPs from the two electrode montages will be recorded simultaneously, so counterbalancing the electrode montage will be unnecessary. A minimum of two amplitude measures will be completed for each electrode montage condition in each position, for a total minimum of 8 recordings per subject. The subject will be given 1-2 minutes to rest their eyes between recordings.
Stimulus level will be calibrated in dBpeak SPL using a 2-cm3 coupler to a sound-level meter (Bruel \& Kjaer). The stimulus waveforms and amplitude spectra will be measured by routing the air conduction output of the sound-level meter to a spectrum analyzer.
Statistical Methods:
Analysis: Summary statistics will be provided for all demographic and clinical variables, along with 95% confidence intervals and side-by-side boxplots. Between-group differences in categorical variables will be assessed via chi-squared tests while differences in continuous variables will be assessed via the Wilcoxin rank-sum test (using significance level alpha = 0.0125 in primary analysis as per the power calculation above). Hotelling's T-squared distribution will also be used as an omnibus or simultaneous test that the groups are the same for all variables in the primary analysis. Amplitude differences obtained using each montage will be calculated as a change expressed in percentage using the formula below:
(n1-p1 amplitude montage2 - n1-p1 amplitude montage 1)
--------------------------------------------------------------- n1-p1 amplitude montage 1
All statistical analyses will be performed with SPSS 23.
Facilities Available: The Vanderbilt Balance Disorders Laboratory is located in the Bill Wilkerson Center. The Balance Disorders Laboratory is equipped with state-of-the art equipment for comprehensive assessment of vestibular and auditory disorders. The facility includes a sound treated room, five diagnostic audiometers, five compact disk players for speech audiometry, five immittance meters, three otoacoustic emissions devices, two rotary vestibular test chairs, three videonystagmography systems, a computerized electronystagmography system, a computerized dynamic posturography system, a Neuroscan evoked response system with capability for 64 channel simultaneous brain signal acquisition, and 4 2-channel clinical evoked potentials systems.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 8
| Arm | Type | Receives |
|---|---|---|
| 20-29 | Experimental | Diagnostic Test: oVEMP - infra-orbital electrode montage, Diagnostic Test: oVEMP - belly-tendon electrode montageParticipants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. |
| 30-39 | Experimental | Diagnostic Test: oVEMP - infra-orbital electrode montage, Diagnostic Test: oVEMP - belly-tendon electrode montageParticipants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. |
| 40-49 | Experimental | Diagnostic Test: oVEMP - infra-orbital electrode montage, Diagnostic Test: oVEMP - belly-tendon electrode montageParticipants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. |
| 50-59 | Experimental | Diagnostic Test: oVEMP - infra-orbital electrode montage, Diagnostic Test: oVEMP - belly-tendon electrode montageParticipants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. |
| 60-69 | Experimental | Diagnostic Test: oVEMP - infra-orbital electrode montage, Diagnostic Test: oVEMP - belly-tendon electrode montageParticipants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. |
| 70-79 | Experimental | Diagnostic Test: oVEMP - infra-orbital electrode montage, Diagnostic Test: oVEMP - belly-tendon electrode montageParticipants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. |
| 80-89 | Experimental | Diagnostic Test: oVEMP - infra-orbital electrode montage, Diagnostic Test: oVEMP - belly-tendon electrode montageParticipants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. |
| 90-99 | Experimental | Diagnostic Test: oVEMP - infra-orbital electrode montage, Diagnostic Test: oVEMP - belly-tendon electrode montageParticipants within the above age range who have normal hearing and no history of balance disorders or unsteadiness. |
Who may qualify
- Ages
- 20 to 99 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Normal hearing and no history of balance disorders
Key exclusion criteria (1 listed)
- Hearing loss, a large amount of ear wax, inner ear of balance problems, and/or no recordable eye muscle responses
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| oVEMP - infra-orbital electrode montageoVEMPs are short latency (~10 ms) stimulus-synchronized extra-ocular muscle reflexes produced in response to appropriate stimuli. The response is believed to originate from excitation of the utricular macula with the subsequent neural response relayed to the brain by the superior portion of the vestibular nerve. Changes in the electrical field of the contralateral inferior oblique muscle can be recorded by an electrode placed at the infra-ocular midline of the lower lid while having the subject gaze upward. The conventional electrode montage, the infra-orbital electrode montage, has the active electrode placed directly inferior to the eye and the reference electrode placed 2-3 cm below the active on the cheek. This electrode montage may result in reference contamination, which will cause an artificially reduced amplitude response, as a portion of the response can be measured by the reference electrode. | Diagnostic test | 20-29, 30-39, 40-49, 50-59, 60-69, 70-79, 80-89, 90-99 |
| oVEMP - belly-tendon electrode montageoVEMPs are short latency (~10 ms) stimulus-synchronized extra-ocular muscle reflexes produced in response to appropriate stimuli. The response is believed to originate from excitation of the utricular macula with the subsequent neural response relayed to the brain by the superior portion of the vestibular nerve. Changes in the electrical field of the contralateral inferior oblique muscle can be recorded by an electrode placed at the infra-ocular midline of the lower lid while having the subject gaze upward. The belly-tendon electrode montage consists of an active electrode placed laterally to the midline of the lower eyelid and a reference electrode placed on the inner canthus. This reference location is believed to be electrically neutral, and should therefore result in larger amplitude responses as the response would not be subject to reference contamination. | Diagnostic test | 20-29, 30-39, 40-49, 50-59, 60-69, 70-79, 80-89, 90-99 |
Primary outcome
Development of Normative Values per Decade
Time frame: 5 months for data collection, one visit per subject.
The oVEMP N1-P1 amplitude and N1 latency will be measured for each subject and will be used to calculate normative values for each decade. The goal is to provide clinics with normative information to base clinical evaluations on.
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Mar 2018.
- Results publication: PubMed 20541460Chang CM, Cheng PW, Wang SJ, Young YH. Effects of repetition rate of bone-conducted vibration on ocular and cervical vestibular-evoked myogenic potentials. Clin Neurophysiol. 2010 Dec;121(12):2121-7. doi: 10.1016/j.clinph.2010.05.013. Epub 2010 Jun 11.
- Results publication: PubMed 17905655Chihara Y, Iwasaki S, Ushio M, Murofushi T. Vestibular-evoked extraocular potentials by air-conducted sound: another clinical test for vestibular function. Clin Neurophysiol. 2007 Dec;118(12):2745-51. doi: 10.1016/j.clinph.2007.08.005. Epub 2007 Oct 1.
- Results publication: PubMed 20709596Curthoys IS, Iwasaki S, Chihara Y, Ushio M, McGarvie LA, Burgess AM. The ocular vestibular-evoked myogenic potential to air-conducted sound; probable superior vestibular nerve origin. Clin Neurophysiol. 2011 Mar;122(3):611-616. doi: 10.1016/j.clinph.2010.07.018. Epub 2010 Aug 14.
- Results publication: PubMed 19464947Govender S, Rosengren SM, Colebatch JG. The effect of gaze direction on the ocular vestibular evoked myogenic potential produced by air-conducted sound. Clin Neurophysiol. 2009 Jul;120(7):1386-91. doi: 10.1016/j.clinph.2009.04.017. Epub 2009 May 22.
- Results publication: PubMed 28520834Makowiec K, McCaslin DL, Jacobson GP, Hatton K, Lee J. Effect of Electrode Montage and Head Position on Air-Conducted Ocular Vestibular Evoked Myogenic Potential. Am J Audiol. 2017 Jun 13;26(2):180-188. doi: 10.1044/2017_AJA-16-0108.
- Results publication: PubMed 23123220Kantner C, Gurkov R. Characteristics and clinical applications of ocular vestibular evoked myogenic potentials. Hear Res. 2012 Dec;294(1-2):55-63. doi: 10.1016/j.heares.2012.10.008. Epub 2012 Oct 30.
- Results publication: PubMed 21993052Murnane OD, Akin FW, Kelly KJ, Byrd S. Effects of stimulus and recording parameters on the air conduction ocular vestibular evoked myogenic potential. J Am Acad Audiol. 2011 Jul-Aug;22(7):469-80. doi: 10.3766/jaaa.22.7.7.
- Results publication: PubMed 20517167Nguyen KD, Welgampola MS, Carey JP. Test-retest reliability and age-related characteristics of the ocular and cervical vestibular evoked myogenic potential tests. Otol Neurotol. 2010 Jul;31(5):793-802. doi: 10.1097/MAO.0b013e3181e3d60e.
- Results publication: PubMed 21586257Piker EG, Jacobson GP, McCaslin DL, Hood LJ. Normal characteristics of the ocular vestibular evoked myogenic potential. J Am Acad Audiol. 2011 Apr;22(4):222-30. doi: 10.3766/jaaa.22.4.5.
- Results publication: PubMed 23673615Piker EG, Jacobson GP, Burkard RF, McCaslin DL, Hood LJ. Effects of age on the tuning of the cVEMP and oVEMP. Ear Hear. 2013 Nov-Dec;34(6):e65-73. doi: 10.1097/AUD.0b013e31828fc9f2.
- Results publication: PubMed 15979939Rosengren SM, McAngus Todd NP, Colebatch JG. Vestibular-evoked extraocular potentials produced by stimulation with bone-conducted sound. Clin Neurophysiol. 2005 Aug;116(8):1938-48. doi: 10.1016/j.clinph.2005.03.019.
- Results publication: PubMed 23333609Sandhu JS, George SR, Rea PA. The effect of electrode positioning on the ocular vestibular evoked myogenic potential to air-conducted sound. Clin Neurophysiol. 2013 Jun;124(6):1232-6. doi: 10.1016/j.clinph.2012.11.019. Epub 2013 Jan 18.
- Individual participant dataSharing planned: No. There is no plan to share IPD with other researchers.
Related trials for Vestibular Abnormality
Recruiting
A Study to Evaluate the Safety and Performance of a Vestibular Implant in Adults to Provide Balance Restoration
Vestibulopathy, Moderate to Severe Hearing Loss
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Kathryn F Makowiec, AuD principal investigator
Vanderbilt University Medical Center
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing oVEMP - infra-orbital electrode montage and oVEMP - belly-tendon electrode montage in people with Vestibular Abnormality and Vestibular Nerve Disorders, run by Vanderbilt University Medical Center at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: withdrawn, as of the sponsor's last update on 15 Mar 2018. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was withdrawn before enrolling participants, so there are no results.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Development of Normative Values per Decade (time frame: 5 months for data collection, one visit per subject.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03251586, which also lists 14 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Mar 2018.