Physiology, Imaging and Modeling of Essential Tremor

Sponsor
University of Florida (Other)
Overall Status
Recruiting
CT.gov ID
NCT03811405
Collaborator
National Institute of Neurological Disorders and Stroke (NINDS) (NIH), Medtronic (Industry)
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Study Details

Study Description

Brief Summary

This project aims to investigate novel ways to deliver brain stimulation to Essential Tremor (ET) patients by introducing software changes to their existing devices. The study team aims to investigate safety and efficacy of these new stimulation parameters in patients with ET.

Condition or Disease Intervention/Treatment Phase
  • Device: Active biphasic pulse stimulation---Home Settings
  • Device: Active biphasic pulse stimulation---VIN Biphasic
  • Device: Active biphasic pulse stimulation---Stimulator Off
N/A

Detailed Description

Deep brain stimulation (DBS) is a neuromodulatory therapy that is effective in a subset of well selected essential tremor (ET) patients. However, as many as 1/5 of patients may initially improve, but then steadily worsen following the operation. The investigators developed a technique to study a variety of alternative stimulation methods without the use of an invasive repeat surgical intervention.

The electrophysiological effects of non-conventional DBS differ from traditional DBS, however the physiological differences in the setting of human tremor remain largely unknown. This study plans to explore gaps in knowledge of neuromodulation and will collect and contribute essential information to the underlying mechanism of action of DBS. The hypothesis of this project centers around active biphasic stimulation providing a wider therapeutic window and a lower adverse event profile as compared to conventional DBS.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Patients with chronically implanted DBS devices for ET who experience progressive worsening of tremor symptoms over time.Patients with chronically implanted DBS devices for ET who experience progressive worsening of tremor symptoms over time.
Masking:
None (Open Label)
Masking Description:
Each of the 3 interventions will be videotaped for blinded motor score assessment by an independent rater.
Primary Purpose:
Treatment
Official Title:
Physiology, Imaging and Modeling of Deep Brain Stimulation for Essential Tremor
Actual Study Start Date :
Apr 1, 2021
Anticipated Primary Completion Date :
Jun 30, 2022
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Patients with Essential Tremor

Patients with chronically implanted DBS devices for ET who experience progressive worsening of tremor symptoms over time. The DBS implantable pulse generator (IPG) will be loaded with a temporary custom firmware to allow implementation of active biphasic pulse stimulation. The following random conditions will be applied: (1) Home Settings; (2) VIN Biphasic; (3) Stimulator Off. A 30-minute washout period will be applied between each of the random conditions. Therefore, each patient will serve as their own control.

Device: Active biphasic pulse stimulation---Home Settings
During this visit, the DBS implantable pulse generator (IPG) will be loaded with a temporary custom firmware to allow implementation of active biphasic pulse stimulation.

Device: Active biphasic pulse stimulation---VIN Biphasic
During this visit, the DBS implantable pulse generator (IPG) will be loaded with a temporary custom firmware to allow implementation of active biphasic pulse stimulation.

Device: Active biphasic pulse stimulation---Stimulator Off
During this visit, the DBS implantable pulse generator (IPG) will be loaded with a temporary custom firmware to allow implementation of active biphasic pulse stimulation.

Outcome Measures

Primary Outcome Measures

  1. Volume of tissue activated from stimulation with ET DBS [up to 24 hours]

    The study team will use computer simulation and virtual reconstruction of the brain from pre-operative MRI data to calculate the volume of tissue activated (VTA) from the novel stimulation patterns. The investigators will assess the feasibility of the patterns to address the worsening of ET that may occur in 20% or more of the ET population.

  2. Baseline DBS settings versus active biphasic pulse DBS settings [up to 1 hour]

    The investigators will compare the degree of tremor suppression from the most optimal DBS settings that can be obtained via traditional programming methods versus active biphasic DBS. The degree of tremor will be quantified by multiple clinical metrics including the Fahn-Tolosa-Marin Tremor Rating Scale and Kinesia ONEĀ® accelerometer system.

Secondary Outcome Measures

  1. The Fahn-Tolosa-Marin Tremor Rating Scale [up to 15 minutes]

    Essential tremor severity will be assessed by the clinically validated Fahn-Tolosa-Marin Tremor Rating Scale (FTMTRS). It is a 0 to 4 scale (0 = no tremor; 4 = severe amplitude of tremor) of 9 different parts of the body. The FTMTRS will be assessed for the various DBS settings.

  2. Tremor motor physiology [up to 15 minutes]

    Essential tremor motor physiology will be recorded by the Kinesia ONE accelerometer system. THe Kinesia ONE system is a wireless wearable motion sensor unit and portable transducer that translates the degree of movement into a standardized scale. Tremor physiology will be assessed for the various DBS settings.

  3. Gait impairment [up to 15 minutes]

    Essential tremor's effect on gait will be assessed by the GAITRite system. Patients will walk along a GAITRite floor mat to have the various gait parameters such as step time, cycle time, step length, stride length, etc measured. Gait parameters will be assessed on the various DBS settings.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Existing unilateral or bilateral VIN DBS for ET, non-demented (MMSE>24), and must have a documented suboptimal tremor suppression on two successive visits (compared to the baseline post-operative improvement at 6 months following ET DBS surgery). For bilateral cases, the most affected tremor side will be studied.
Exclusion Criteria:
  • No diagnosis of Essential Tremor

Contacts and Locations

Locations

Site City State Country Postal Code
1 UF Health at the University of Florida Gainesville Florida United States 32610
2 McKnight Brain Institute--Fixel Center for Neurological Diseases Gainesville Florida United States 32611

Sponsors and Collaborators

  • University of Florida
  • National Institute of Neurological Disorders and Stroke (NINDS)
  • Medtronic

Investigators

  • Principal Investigator: Leonardo B Almeida, MD, Univeristy of Florida

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Florida
ClinicalTrials.gov Identifier:
NCT03811405
Other Study ID Numbers:
  • IRB201802397 -N -A
  • OCR19607
  • 1R25NS108939-01
  • 5R25NS108939-03
  • MEDTRONIC INC
First Posted:
Jan 22, 2019
Last Update Posted:
Feb 17, 2022
Last Verified:
Feb 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Keywords provided by University of Florida
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 17, 2022