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Physiology, Imaging and Modeling of Essential Tremor

Primary Purpose

Essential Tremor, Parkinson Disease, Dystonia

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Active biphasic pulse stimulation---Home Settings
Active biphasic pulse stimulation---VIN Biphasic
Active biphasic pulse stimulation---Stimulator Off
Sponsored by
University of Florida
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Essential Tremor focused on measuring Deep Brain Stimulation (DBS), ventralis intermedius nucleus (VIN), implantable pulse generator (IPG), Diffusion Tensor Imaging (DTI)

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • UF Health at the University of FloridaRecruiting
  • McKnight Brain Institute--Fixel Center for Neurological Diseases

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Patients with Essential Tremor

Arm Description

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.

Outcomes

Primary Outcome Measures

Volume of tissue activated from stimulation with ET DBS
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.
Baseline DBS settings versus active biphasic pulse DBS settings
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 ONE® accelerometer system.

Secondary Outcome Measures

The Fahn-Tolosa-Marin Tremor Rating Scale
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.
Tremor motor physiology
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.
Gait impairment
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.

Full Information

First Posted
January 17, 2019
Last Updated
June 13, 2023
Sponsor
University of Florida
Collaborators
National Institute of Neurological Disorders and Stroke (NINDS), Medtronic
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1. Study Identification

Unique Protocol Identification Number
NCT03811405
Brief Title
Physiology, Imaging and Modeling of Essential Tremor
Official Title
Physiology, Imaging and Modeling of Deep Brain Stimulation for Essential Tremor
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2021 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
June 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Florida
Collaborators
National Institute of Neurological Disorders and Stroke (NINDS), Medtronic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No

5. 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Essential Tremor, Parkinson Disease, Dystonia
Keywords
Deep Brain Stimulation (DBS), ventralis intermedius nucleus (VIN), implantable pulse generator (IPG), Diffusion Tensor Imaging (DTI)

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
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.
Allocation
N/A
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Patients with Essential Tremor
Arm Type
Experimental
Arm Description
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.
Intervention Type
Device
Intervention Name(s)
Active biphasic pulse stimulation---Home Settings
Intervention Description
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.
Intervention Type
Device
Intervention Name(s)
Active biphasic pulse stimulation---VIN Biphasic
Intervention Description
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.
Intervention Type
Device
Intervention Name(s)
Active biphasic pulse stimulation---Stimulator Off
Intervention Description
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.
Primary Outcome Measure Information:
Title
Volume of tissue activated from stimulation with ET DBS
Description
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.
Time Frame
up to 24 hours
Title
Baseline DBS settings versus active biphasic pulse DBS settings
Description
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 ONE® accelerometer system.
Time Frame
up to 1 hour
Secondary Outcome Measure Information:
Title
The Fahn-Tolosa-Marin Tremor Rating Scale
Description
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.
Time Frame
up to 15 minutes
Title
Tremor motor physiology
Description
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.
Time Frame
up to 15 minutes
Title
Gait impairment
Description
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.
Time Frame
up to 15 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Leonardo B Almeida, MD
Phone
(352) 294-5400
Email
Leonardo.BritodeAlmeida@neurology.ufl.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Joshua K Wong, MD
Phone
(352) 294-5400
Email
joshua.wong@neurology.ufl.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leonardo B Almeida, MD
Organizational Affiliation
Univeristy of Florida
Official's Role
Principal Investigator
Facility Information:
Facility Name
UF Health at the University of Florida
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32610
Country
United States
Individual Site Status
Recruiting
Facility Name
McKnight Brain Institute--Fixel Center for Neurological Diseases
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32611
Country
United States
Individual Site Status
Not yet recruiting

12. IPD Sharing Statement

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Physiology, Imaging and Modeling of Essential Tremor

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