Essential TremorNCT05362448
Neurophysiologic Assessment of ET Patients Treated by Vim DBS
A study testing Frequency in people with Essential Tremor, run by University College London Hospitals at 1 site in United Kingdom.
Trial summary
Essential tremor is a chronic and progressive neurological disease characterized by upper limb tremor. This is one of the most frequent movement disorders. Most of the time the disease worsens over the time, affecting patients' work abilities and in the most severe cases activities of daily living such as eating or… Read more about this study
- Who is it for?
- Ages 18 to 90 years
- Conditions the study is for
- Essential Tremor
- What is being tested?
- Frequency
- Type of treatment
- Medical device
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 20 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 23 May 2022to 1 Nov 2022
- 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 18 to 90 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age > 18 years
- No gender specification
- Patient suffering from severe medically intractable essential tremor and treated by Vim-DBS
- Willing and able to provide written informed consent
Who cannot join
- Concurrent and/or recent involvement in other research that is likely to interfere with the intervention within the last 3 months before study enrolment
- Patients presenting with other cause(s) of balance or gait disorders (stroke, concomitant neurological, rheumatological or orthopaedic disease, severe hypopallesthesia, visual impairment, neuromuscular or vestibular disorders)
- Recently implanted patients (<3 months)
- Patients unable to provide written informed consent (patients presenting with psychiatric or cognitive disorders)
Trial locations and contacts
1 site in 1 country.
United Kingdom1 site, 1 recruiting
- Recruiting
National Hospital for Neurology and Neurosurgery
London, England, WC1N 3BG
Patricia Limousin, MD PhD, 0203 448 8723 ext. +44, p.limousin@ucl.ac.uk
Thomas Wirth, MD MS, 0203 448 8723 ext. +44, t.wirth@nhs.net
About this study
Official title: Assessment of Cerebellar Ataxia Associated With Ventral Intermediate Median Nucleus Deep Brain Stimulation in Essential Tremor: a Multimodal Neurophysiologic Study
Essential tremor is a chronic and progressive neurological disease characterized by upper limb tremor. This is one of the most frequent movement disorders. Most of the time the disease worsens over the time, affecting patients' work abilities and in the most severe cases activities of daily living such as eating or dressing. For the most disabled patients, Deep brain stimulation (DBS) of the thalamic ventral intermediate median nucleus (Vim), a procedure consisting in an electrode implantation in a structure of the brain involved in tremor genesis, is the gold standard treatment. While this therapy is most of the time highly effective in alleviating the tremor, some subjects may exhibit gait impairment or upper limb coordination troubles years after the surgery, which are thought to be due to the involuntary stimulation of efferent cerebellar fiber tract. Unfortunately, this DBS induced side effect cannot be systematically avoided and may limit the possibilities of settings adaptation required to control the tremor. Surprisingly, while it could be a valuable therapeutic option for these patients suffering from DBS induced balance troubles, little is known about the effect of varying the rate of stimulation on the gait disorders associated with essential tremor and Vim DBS. The aim of or study is consequently to assess the effect of different frequency of stimulation on tremor, gait and balance disorders as well as on eye movements in patients uni or bilaterally stimulated in the Vim for a severe and medically intractable essential tremor. Patients followed at the National Hospital for Neurology and Neurosurgery (University College London Hospital) will be included. To better characterize the different symptoms, the investigators will use ataxia and tremor rating scale together with 3D gait motion analysis, oculography and computerized spiral test analysis. Our findings might lead to a better understanding of Vim-DBS associated gait disorders in essential tremor.
Read the detailed description
Essential tremor (ET) is a chronic, progressive neurological disease characterized by a symmetrical 4-12 Hz kinetic tremor constantly affecting hands and arms. The tremor can also involve the neck, the lower limb, the voice, the mouth, the tongue or other body regions. ET is among the most frequent movement disorders, with an estimated prevalence of 0,9% of the global population. While the tremor can be mildly disabling at the beginning of the disease, most patients experience a worsening of their tremor over the time. Eventually, disease progression can lead to severe disability, impacting patients' working abilities and in the most severe cases, activity of daily living. Though ET being a frequent debilitating condition, there are still few therapeutic options for the most disabled patients. Several surgical procedures have been evaluated in ET including Deep brain Stimulation (DBS) of Thalamic Ventral intermediate nucleus (Vim) or within the posterior subthalamic area, surgical thalamotomy, Gamma knife or, more recently, MRI guided focused ultrasound thalamotomy. While Gamma knife and focused ultrasound thalamotomy may be safer due to the absence of craniotomy, Vim-DBS remains currently the reference treatment and the most used procedure for medically refractory ET.
Besides the early side effects of Vim-DBS such as haemorrhagic, ischemic and infectious complications occurring immediately after the electrodes implantation procedure, late side-effects such as cerebellar symptoms including gait or upper limb cerebellar ataxia, paraesthesia, dysarthria, dysphagia, and cognitive difficulties are quite frequent. These long-term consequences of the stimulation may dramatically impact the quality of life of patients suffering from ET years after the surgery and mitigate the benefits of this intervention. Considering gait ataxia, it has been reported that this complication may affect up to 37% of ET patients following Vim-DBS surgery and seem to occur more frequently in patient who had pre-operative gait impairment, greater disease severity, older age and when DBS was performed bilaterally. Upper limb ataxia is also common and characterized by the occurrence or the paradoxical worsening of an intention tremor together with asynergy, dyschronometria and dysdiadochokinesia. It has been shown that this latter can be induced by suprathreshold stimulation.
One of the major assets of Vim-DBS over surgical thalamotomy remain its ability to steadily adapt the current delivered by the electrodes by changing the stimulation parameters. Using traditional Implantable Pulse Generator (IPG), it is possible to modify the stimulation mode (monopolar or bipolar stimulation), amplitude, frequency and pulse width as well as to modify the contacts of the electrodes delivering the current. However, despite DBS being a treatment largely available worldwide as well as being part of the routine care for medically refractory tremor, only few studies have assessed the effects of varying DBS settings on cerebellar symptoms presented by patients suffering from ET and stimulated within the Vim. It has been reported that tremor responds best to amplitude, which is usually increased until a complete resolution of the tremor is obtained. Increasing the stimulation pulse width produces a similar clinical effect and may help to alleviate tremor. Interestingly, it has recently been shown that decreasing the pulse width may improve the gait disorders, widen the therapeutic window and diminishes DBS induced side effects. This clinical finding is supported by the recent dissection of the neuronal network underlying Vim DBS clinical response which suggest that tremor suppression could be due to dentato-rubro-thalamic tract stimulation while gait and limb ataxia could be promoted by the stimulation of the cerebello-rubro-spinal and the rubro-olivo-cerebellar tract meaning the possibility of correcting these side effects by accurately optimizing the DBS parameters.
Among the clinical effect of the different types of parameters, the stimulation frequency has certainly been the less extensively studied in ET. This is at first sight quite surprising given that decreasing the frequency of stimulation of the Subthalamic nucleus (STN) is a valuable therapeutic option in Parkinson's disease especially for patient presenting with dopa-refractory symptoms such as freezing of gait or speech impairment. Lower frequency stimulation has also shown to be beneficial for some patients suffering from dystonia, and it has been suggested that this sustained clinical improvement was obtained by avoiding the stimulation of the structure responsible of side effects.
In comparison, a very low number of studies has focused on the consequences of lower frequency stimulation on tremor. Noteworthy is the fact that most of them have pointed that the tremor suppression was better achieved for a frequency around 100 Hz, with little evidence for a small additional therapeutic effect for frequencies above 130 Hz. Conversely, frequency of 50 Hz or lower seems to not suppress tremor and could even worsen it or induce myoclonic jerks. Based on these clinical findings, it is currently admitted initiating the stimulation with a frequency of 130 Hz and increasing it up to 180 Hz if the therapeutic effect on tremor remains unsatisfying despite concomitant high amplitude and large pulse width. A recent small case series has interestingly shown that some patients presenting with balance disorder years after Vim DBS surgery were having their trouble improved when the stimulation frequency was decreased to 130 Hz. Additionally, there are some evidence that, similarly to short pulse width stimulation, decreasing the frequency up to 100 Hz may help to optimize postural or intention tremor and DBS side effects control by widening the therapeutic window. Taken together, these findings suggest that, similarly to shorter pulse width, a lower frequency of stimulation could be an interesting therapeutic approach for ET patients suffering from balance disorders or upper limb ataxia promoted by Vim-DBS. However, since all the above-mentioned studies were unblinded and non-randomized, the level of evidence supporting such a strategy remain weak. Additionally, none of these works has aimed at evaluating the effect of decreasing DBS frequency on gait and balance, neither by using clinical testing, nor by using quantitative measurement such as 3D motion analysis or computerized posture assessment.
For these reasons, the aim of the present study will be to study the effect of varying Vim-DBS frequency on cerebellar features including gait and upper limb ataxia in ET by using non-invasive quantitative physiological tools, namely computerized spiral test analysis, 3D infrared gait motion analysis, balance measure against force perturbation analysis and oculography.
Patients presenting an ET treated by Vim-DBS stimulation for more than 3 months, followed at the National Hospital of Neurology and Neurosurgery, University College London Hospital, London, United Kingdom will be included.
Regarding the procedure, the investigators will first assess the therapeutic window by estimating the therapeutic and side effect thresholds for three different frequencies (80 Hz-130 Hz-180 Hz). Additionally, the investigators will subsequently analyse balance and gait using a 3D motion analysis system, the tremor using a tablet coupled to a computerized spiral analysis software and eye movements using oculography for the three different settings and with the DBS turned off.
Eventually, the investigators will localize the position of the electrodes and model Volume of Tissue Activated using the DBS planning software Guide-XT® and the pre and postoperative brain MRI.
- Conditions
- Essential Tremor
- Being tested
- Frequency
- Keywords
- Deep brain Stimulation, Ventral Intermediate nucleus, Gait motion analysis, Balance against force perturbation analysis, Computerized spiral test analysis, Frequency
- Medical subject headings
- Essential Tremor
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
FrequencyDevice
First, we will calculate for each patient and each frequency the amplitude therapeutic window (difference between therapeutic and side effect threshold). We will determine an optimal amplitude for each frequency that we will apply in the second part of the study.
| Study group | Role | What they receive |
|---|---|---|
| 80 Hz | Active comparator | Stimulation with a frequency of 80 Hz Receives: Device: Frequency |
| 130 Hz | Active comparator | Stimulation with a frequency of 130 Hz Receives: Device: Frequency |
| 180 Hz | Active comparator | Stimulation with a frequency of 180 Hz Receives: Device: Frequency |
| DBS off | Sham comparator | Absence of stimulation Receives: Device: Frequency |
What is being measured
The primary outcome is the main question the study is designed to answer.
Center of Pressure Displacement
Quantitative continuous variable assessed using balance against force perturbation analysis under the three different DBS settings conditions and with the DBS switched off
Measured: 1 day
Secondary outcomes (24)
Side effect threshold
Amplitude of DBS stimulation needed to induce side effects under the three DBS settings conditions
Measured: 1 day
Therapeutic threshold
Amplitude of DBS stimulation needed to correct tremor under the three DBS settings conditions
Measured: 1 day
Therapeutic window
Difference between side effect threshold and therapeutic threshold under the three DBS settings conditions
Measured: 1 day
Total Energy Delivered
Energy delivered by the pulse generator under the three different DBS settings conditions
Measured: 1 day
Charge density
Charge delivered by the pulse generator under the three different DBS settings conditions
Measured: 1 day
Scale for the Assessment and Rating of Ataxia score
Scoring of cerebellar ataxia under the three different DBS settings conditions and with the DBS switched off
Measured: 1 day
Tremor rating scale score
Scoring of tremor severity under the three different DBS settings conditions and with the DBS switched off
Measured: 1 day
Volume of Tissue Activated
Prediction through imaging of the volume of tissue activated by stimulation under the three different DBS settings conditions
Measured: 1 day
Computerized spiral test analysis (SWVI)
Comparison of spiral width variability index (SWVI) between the four different conditions
Measured: 1 day
Computerized spiral test analysis (AUC)
Comparison of the Area under the curve (AUC) of the acceleration after Fast Fourier Transform between the four different conditions
Measured: 1 day
Computerized spiral test analysis (tremor frequency)
Comparison of the tremor frequency between the four different conditions
Measured: 1 day
Balance motion analysis (CoP initial position)
Comparison of the center of pressure (CoP) initial position and the resisting force between the four different conditions
Measured: 1 day
Balance motion analysis (resisting force)
Comparison of the resisting force between the four different conditions
Measured: 1 day
Gait motion analysis (step length)
Comparison of step length between the four different conditions
Measured: 1 day
Gait motion analysis (number of steps)
Comparison of the number of steps between the four different conditions
Measured: 1 day
Gait motion analysis (stride length)
Comparison of the stride length between the four different conditions
Measured: 1 day
Gait motion analysis (stride velocity)
Comparison of the stride velocity between the four different conditions
Measured: 1 day
Gait motion analysis (normalized double support time)
Comparison of the normalized double support time between the four different conditions
Measured: 1 day
Gait motion analysis (step length asymmetry)
Comparison of the step length asymmetry between the four different conditions
Measured: 1 day
Oculography (fixation index)
Comparison of the fixation index between the four different conditions using eye tracking system
Measured: 1 day
Oculography (saccades velocity)
Comparison of saccades velocity between the four different conditions using eye tracking system
Measured: 1 day
Oculography (saccades latency)
Comparison of saccades latency (ms) between the four different conditions using eye tracking system
Measured: 1 day
Oculography (saccades accuracy index)
Comparison of saccades accuracy index between the four different conditions using eye tracking system
Measured: 1 day
Oculography (VOR gain)
Comparison of the vestibulo-ocular reflex gain (VOR) between the four different conditions using eye tracking system
Measured: 1 day
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 May 2022
- Study start23 May 2022
- Primary completion1 Nov 2022 (estimated)
- Study completion1 Nov 2022 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Essential TremorStudies of the same condition, open and under way.
- 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
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Triple blind
- Who is masked
- Participant, Investigator, Outcomes assessor
- Enrolment
- 20 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University College London Hospitals
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Thomas Wirth, University College London Hospitals
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05362448
- Sponsor's protocol ID
- 274481
- Status last verified
- May 2022
- First submitted
- 11 Apr 2022
- Last updated
- 27 May 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 27 May 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Assessment of Cerebellar Ataxia Associated With Ventral Intermediate Median Nucleus Deep Brain Stimulation in Essential Tremor: a Multimodal Neurophysiologic Study
- ClinicalTrials.gov ID
- NCT05362448
- Acronym / sponsor ID
- 274481
- Conditions
- Essential Tremor
- Keywords
- Deep brain Stimulation, Ventral Intermediate nucleus, Gait motion analysis, Balance against force perturbation analysis, Computerized spiral test analysis, Frequency
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 20 participants (estimated)
- Lead sponsor
- University College London HospitalsUniversity, hospital or other
- Study start
- 23 May 2022 (actual)
- Primary completion
- 1 Nov 2022 (estimated)
- Study completion
- 1 Nov 2022 (estimated)
- First posted
- 5 May 2022 (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.
Essential tremor is a chronic and progressive neurological disease characterized by upper limb tremor. This is one of the most frequent movement disorders. Most of the time the disease worsens over the time, affecting patients' work abilities and in the most severe cases activities of daily living such as eating or dressing. For the most disabled patients, Deep brain stimulation (DBS) of the thalamic ventral intermediate median nucleus (Vim), a procedure consisting in an electrode implantation in a structure of the brain involved in tremor genesis, is the gold standard treatment. While this therapy is most of the time highly effective in alleviating the tremor, some subjects may exhibit gait impairment or upper limb coordination troubles years after the surgery, which are thought to be due to the involuntary stimulation of efferent cerebellar fiber tract. Unfortunately, this DBS induced side effect cannot be systematically avoided and may limit the possibilities of settings adaptation required to control the tremor. Surprisingly, while it could be a valuable therapeutic option for these patients suffering from DBS induced balance troubles, little is known about the effect of varying the rate of stimulation on the gait disorders associated with essential tremor and Vim DBS. The aim of or study is consequently to assess the effect of different frequency of stimulation on tremor, gait and balance disorders as well as on eye movements in patients uni or bilaterally stimulated in the Vim for a severe and medically intractable essential tremor. Patients followed at the National Hospital for Neurology and Neurosurgery (University College London Hospital) will be included. To better characterize the different symptoms, the investigators will use ataxia and tremor rating scale together with 3D gait motion analysis, oculography and computerized spiral test analysis. Our findings might lead to a better understanding of Vim-DBS associated gait disorders in essential tremor.
Detailed description
Essential tremor (ET) is a chronic, progressive neurological disease characterized by a symmetrical 4-12 Hz kinetic tremor constantly affecting hands and arms. The tremor can also involve the neck, the lower limb, the voice, the mouth, the tongue or other body regions. ET is among the most frequent movement disorders, with an estimated prevalence of 0,9% of the global population. While the tremor can be mildly disabling at the beginning of the disease, most patients experience a worsening of their tremor over the time. Eventually, disease progression can lead to severe disability, impacting patients' working abilities and in the most severe cases, activity of daily living. Though ET being a frequent debilitating condition, there are still few therapeutic options for the most disabled patients. Several surgical procedures have been evaluated in ET including Deep brain Stimulation (DBS) of Thalamic Ventral intermediate nucleus (Vim) or within the posterior subthalamic area, surgical thalamotomy, Gamma knife or, more recently, MRI guided focused ultrasound thalamotomy. While Gamma knife and focused ultrasound thalamotomy may be safer due to the absence of craniotomy, Vim-DBS remains currently the reference treatment and the most used procedure for medically refractory ET.
Besides the early side effects of Vim-DBS such as haemorrhagic, ischemic and infectious complications occurring immediately after the electrodes implantation procedure, late side-effects such as cerebellar symptoms including gait or upper limb cerebellar ataxia, paraesthesia, dysarthria, dysphagia, and cognitive difficulties are quite frequent. These long-term consequences of the stimulation may dramatically impact the quality of life of patients suffering from ET years after the surgery and mitigate the benefits of this intervention. Considering gait ataxia, it has been reported that this complication may affect up to 37% of ET patients following Vim-DBS surgery and seem to occur more frequently in patient who had pre-operative gait impairment, greater disease severity, older age and when DBS was performed bilaterally. Upper limb ataxia is also common and characterized by the occurrence or the paradoxical worsening of an intention tremor together with asynergy, dyschronometria and dysdiadochokinesia. It has been shown that this latter can be induced by suprathreshold stimulation.
One of the major assets of Vim-DBS over surgical thalamotomy remain its ability to steadily adapt the current delivered by the electrodes by changing the stimulation parameters. Using traditional Implantable Pulse Generator (IPG), it is possible to modify the stimulation mode (monopolar or bipolar stimulation), amplitude, frequency and pulse width as well as to modify the contacts of the electrodes delivering the current. However, despite DBS being a treatment largely available worldwide as well as being part of the routine care for medically refractory tremor, only few studies have assessed the effects of varying DBS settings on cerebellar symptoms presented by patients suffering from ET and stimulated within the Vim. It has been reported that tremor responds best to amplitude, which is usually increased until a complete resolution of the tremor is obtained. Increasing the stimulation pulse width produces a similar clinical effect and may help to alleviate tremor. Interestingly, it has recently been shown that decreasing the pulse width may improve the gait disorders, widen the therapeutic window and diminishes DBS induced side effects. This clinical finding is supported by the recent dissection of the neuronal network underlying Vim DBS clinical response which suggest that tremor suppression could be due to dentato-rubro-thalamic tract stimulation while gait and limb ataxia could be promoted by the stimulation of the cerebello-rubro-spinal and the rubro-olivo-cerebellar tract meaning the possibility of correcting these side effects by accurately optimizing the DBS parameters.
Among the clinical effect of the different types of parameters, the stimulation frequency has certainly been the less extensively studied in ET. This is at first sight quite surprising given that decreasing the frequency of stimulation of the Subthalamic nucleus (STN) is a valuable therapeutic option in Parkinson's disease especially for patient presenting with dopa-refractory symptoms such as freezing of gait or speech impairment. Lower frequency stimulation has also shown to be beneficial for some patients suffering from dystonia, and it has been suggested that this sustained clinical improvement was obtained by avoiding the stimulation of the structure responsible of side effects.
In comparison, a very low number of studies has focused on the consequences of lower frequency stimulation on tremor. Noteworthy is the fact that most of them have pointed that the tremor suppression was better achieved for a frequency around 100 Hz, with little evidence for a small additional therapeutic effect for frequencies above 130 Hz. Conversely, frequency of 50 Hz or lower seems to not suppress tremor and could even worsen it or induce myoclonic jerks. Based on these clinical findings, it is currently admitted initiating the stimulation with a frequency of 130 Hz and increasing it up to 180 Hz if the therapeutic effect on tremor remains unsatisfying despite concomitant high amplitude and large pulse width. A recent small case series has interestingly shown that some patients presenting with balance disorder years after Vim DBS surgery were having their trouble improved when the stimulation frequency was decreased to 130 Hz. Additionally, there are some evidence that, similarly to short pulse width stimulation, decreasing the frequency up to 100 Hz may help to optimize postural or intention tremor and DBS side effects control by widening the therapeutic window. Taken together, these findings suggest that, similarly to shorter pulse width, a lower frequency of stimulation could be an interesting therapeutic approach for ET patients suffering from balance disorders or upper limb ataxia promoted by Vim-DBS. However, since all the above-mentioned studies were unblinded and non-randomized, the level of evidence supporting such a strategy remain weak. Additionally, none of these works has aimed at evaluating the effect of decreasing DBS frequency on gait and balance, neither by using clinical testing, nor by using quantitative measurement such as 3D motion analysis or computerized posture assessment.
For these reasons, the aim of the present study will be to study the effect of varying Vim-DBS frequency on cerebellar features including gait and upper limb ataxia in ET by using non-invasive quantitative physiological tools, namely computerized spiral test analysis, 3D infrared gait motion analysis, balance measure against force perturbation analysis and oculography.
Patients presenting an ET treated by Vim-DBS stimulation for more than 3 months, followed at the National Hospital of Neurology and Neurosurgery, University College London Hospital, London, United Kingdom will be included.
Regarding the procedure, the investigators will first assess the therapeutic window by estimating the therapeutic and side effect thresholds for three different frequencies (80 Hz-130 Hz-180 Hz). Additionally, the investigators will subsequently analyse balance and gait using a 3D motion analysis system, the tremor using a tablet coupled to a computerized spiral analysis software and eye movements using oculography for the three different settings and with the DBS turned off.
Eventually, the investigators will localize the position of the electrodes and model Volume of Tissue Activated using the DBS planning software Guide-XT® and the pre and postoperative brain MRI.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| 80 Hz | Active comparator | Device: FrequencyStimulation with a frequency of 80 Hz |
| 130 Hz | Active comparator | Device: FrequencyStimulation with a frequency of 130 Hz |
| 180 Hz | Active comparator | Device: FrequencyStimulation with a frequency of 180 Hz |
| DBS off | Sham comparator | Device: FrequencyAbsence of stimulation |
Who may qualify
- Ages
- 18 to 90 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Age > 18 years
- No gender specification
- Patient suffering from severe medically intractable essential tremor and treated by Vim-DBS
- Willing and able to provide written informed consent
Key exclusion criteria (4 listed)
- Concurrent and/or recent involvement in other research that is likely to interfere with the intervention within the last 3 months before study enrolment
- Patients presenting with other cause(s) of balance or gait disorders (stroke, concomitant neurological, rheumatological or orthopaedic disease, severe hypopallesthesia, visual impairment, neuromuscular or vestibular disorders)
- Recently implanted patients (<3 months)
- Patients unable to provide written informed consent (patients presenting with psychiatric or cognitive disorders)
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 |
|---|---|---|
| FrequencyFirst, we will calculate for each patient and each frequency the amplitude therapeutic window (difference between therapeutic and side effect threshold). We will determine an optimal amplitude for each frequency that we will apply in the second part of the study. | Device | 130 Hz, 180 Hz, 80 Hz, DBS off |
Primary outcome
Center of Pressure Displacement
Time frame: 1 day
Quantitative continuous variable assessed using balance against force perturbation analysis under the three different DBS settings conditions and with the DBS switched off
24 secondary outcomes
Side effect threshold
Time frame: 1 day
Therapeutic threshold
Time frame: 1 day
Therapeutic window
Time frame: 1 day
Total Energy Delivered
Time frame: 1 day
Charge density
Time frame: 1 day
Scale for the Assessment and Rating of Ataxia score
Time frame: 1 day
Tremor rating scale score
Time frame: 1 day
Volume of Tissue Activated
Time frame: 1 day
Computerized spiral test analysis (SWVI)
Time frame: 1 day
Computerized spiral test analysis (AUC)
Time frame: 1 day
Computerized spiral test analysis (tremor frequency)
Time frame: 1 day
Balance motion analysis (CoP initial position)
Time frame: 1 day
Balance motion analysis (resisting force)
Time frame: 1 day
Gait motion analysis (step length)
Time frame: 1 day
Gait motion analysis (number of steps)
Time frame: 1 day
Gait motion analysis (stride length)
Time frame: 1 day
Gait motion analysis (stride velocity)
Time frame: 1 day
Gait motion analysis (normalized double support time)
Time frame: 1 day
Gait motion analysis (step length asymmetry)
Time frame: 1 day
Oculography (fixation index)
Time frame: 1 day
Oculography (saccades velocity)
Time frame: 1 day
Oculography (saccades latency)
Time frame: 1 day
Oculography (saccades accuracy index)
Time frame: 1 day
Oculography (VOR gain)
Time frame: 1 day
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 May 2022.
- Individual participant dataSharing planned: No
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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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Frequency in people with Essential Tremor, run by University College London Hospitals at 1 site in United Kingdom.
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 4 inclusion and 4 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: status not confirmed, as of the sponsor's last update on 27 May 2022. 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 Kingdom. 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. Some participants in this study may receive a placebo. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Patricia Limousin, MD PhD (02034567890 ext. +44, p.limousin@ucl.ac.uk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Center of Pressure Displacement (time frame: 1 day). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 27 May 2022.