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Dual Frequency Stimulation in Parkinson's Disease

Primary Purpose

Parkinson Disease

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Deep brain stimulation
Sponsored by
University of California, Davis
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson Disease focused on measuring DBS, Deep Brain Stimulation, STN, Subthalamic Nucleus, Parkinson disease, Dual frequency, Dual region, DFDR

Eligibility Criteria

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

Inclusion Criteria:

  • Individuals who are 18 years and older
  • Individuals with idiopathic Parkinson's Disease who previously underwent implantation with the Boston Scientific VerciseTM DBS system
  • Individuals who have been implanted with the Boston Scientific VerciseTM DBS system for at least 3 months
  • Individuals diagnosed with advanced PD who had bilateral dorsal subthalamic nucleus DBS surgery, as standard of care for motor improvement, with distal contacts of the electrodes implanted into the ventral STN

Exclusion Criteria:

  • Individuals unable to provide consent and/or lack capacity to consent
  • Individuals diagnosed with any cognitive or physical impairments that would limit their ability to participate in the cognitive testing
  • Individuals who score below 15 on the Montreal Cognitive Assessment Test-Blind
  • Individuals who score above 20 on the Center for Epidemiologic Studies Depression Scale
  • Pregnant women (note: pregnant women are not candidates for DBS surgery), and prisoners
  • Non-English speaking individuals. Cognitive tasks will only be conducted in English.

Sites / Locations

  • UC Davis HealthRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Sustained Dual Frequency, Dual Region, Stimulation

Arm Description

Outcomes

Primary Outcome Measures

Mean Change from Baseline in Depression Scores on the Center for Epidemiologic Studies Depression Scale (CES-D)
The score of the CES-D will be compared across sessions and a score that rises above 20 (out of 60) will be considered positive for the development of depression.
Mean Change from Baseline in Impulsiveness Scores on the Barratt Impulsiveness Scale (BIS-11)
The score of the BIS-11 will be evaluated across sessions and elevated scores indicate greater impulsivity and risk-taking behavior. The scale involves 30 questions with values from 1-4. Overall scores range from 30-120.
Mean Change from Baseline in Neuropsychiatric Inventory (NPI)
The NPI assesses frequency, change in severity, and distress over 12 neuropsychiatric domains as evaluated by the caregiver. We will look for a significant score reduction in any domain of the NPI.
Mean Change from Baseline in Movement Scores on Part III of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS)
Part III of the MDS-UPDRS consists of 18 areas of motor assessments to assess severity of symptoms. Each score is rated in terms of severity from 0-4, with higher scores indicating higher severity of symptoms. A composite score will be evaluated for changes from baseline.
Mean Change from Baseline in Cognitive Performance Scores on the Montreal Cognitive Assessment - Blind (MoCA)
This will be collected via telephone calls. The MoCA-Blind has been validated for telephone administration. We will re-evaluate MoCA-Blind scores during telephone monitoring to assess any changes to cognitive ability. A total score of less than 15 out of a possible 22 indicates greater than mild cognitive impairment.
Mean Change from Baseline in Depression Scores on the CES-D Short Version (CES-D-R10)
This will be collected via telephone calls. Patients will be given an unmarked form with questions and will be able to follow along the telephone conversation and answer each question (0-4 severity rating scale) for 10 questions focused on patient affect. A total score greater than 10 (out of 30) indicates the development of depression symptoms.
Mean Change from Baseline in Motor and Non-Motor Aspects of Daily Living Scores on Parts I and II of the MDS-UPDRS
This will be collected via telephone calls. Patients will be asked questions relating to motor and non-motor aspects of daily living and to rate the severity of their symptoms on a scale from 0-4, with higher scores indicating higher severity of symptoms. We will assess for changes in the composite score from baseline.

Secondary Outcome Measures

Mean Change from Baseline in Decision-Making Scores on Probabilistic Gambling Task
A patient-specific measure of risk attitude during a gambling task. We will estimate indifference points (win probability at which risky choice is chosen 50% of the time) at each time point and compare to those points during baseline performance on the task.
Mean Change from Baseline in Inter-Temporal Choice Scores on a Temporal Discounting Task
A patient-specific measure of risk attitude during a temporal preferences task. We will examine the area under the curve of the empirical discount functions of 'larger later' rewards and 'smaller sooner' rewards. Smaller values indicate increased preference for smaller sooner over larger later rewards. Scores will be compared to baseline performance on the task.
Mean Change from Baseline in Verbal Fluency Scores on Word Generation Task
The average number of words generated in a 1-minute time frame.

Full Information

First Posted
November 16, 2020
Last Updated
December 21, 2022
Sponsor
University of California, Davis
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1. Study Identification

Unique Protocol Identification Number
NCT04650932
Brief Title
Dual Frequency Stimulation in Parkinson's Disease
Official Title
Dual Frequency, Dual Region Deep Brain Stimulation of the Subthalamic Nucleus in Parkinson's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 22, 2022 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, Davis

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Deep brain stimulation (DBS) in the dorsal region of the subthalamic nucleus (STN) is very effective for reducing motor symptoms of Parkinson's disease (PD). Modeling studies suggest that this therapy may result in current spread into the ventral STN, causing altered cognitive processes. As a result, current stimulation parameters often lead to worsening in verbal fluency, executive function, and, particularly, cognitive control. There is evidence suggesting that low frequency oscillatory activity occurs across brain circuits important in integrating information for cognition. Preclinical studies and human recording studies indicate these low frequency theta oscillations drive cognitive control during cognitive tasks. Thus, the purpose of this study is to determine the safety, tolerability, and efficacy of low frequency stimulation (LFS) of the ventral STN alongside standard high frequency stimulation (HFS) of the dorsal STN in patients with PD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease
Keywords
DBS, Deep Brain Stimulation, STN, Subthalamic Nucleus, Parkinson disease, Dual frequency, Dual region, DFDR

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Masking Description
Open-label
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sustained Dual Frequency, Dual Region, Stimulation
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Deep brain stimulation
Other Intervention Name(s)
Boston Scientific Vercise DBS
Intervention Description
Patients with idiopathic Parkinson's disease who have previously been implanted with the Boston Scientific VerciseTM DBS system for at least 3 months. These patients will already be receiving high-frequency dorsal STN stimulation as part of the standard of care for PD. Once patients have provided consent and are enrolled in this study, they will receive simultaneous low-frequency stimulation of the ventral STN to examine if there are any effects on cognitive performance.
Primary Outcome Measure Information:
Title
Mean Change from Baseline in Depression Scores on the Center for Epidemiologic Studies Depression Scale (CES-D)
Description
The score of the CES-D will be compared across sessions and a score that rises above 20 (out of 60) will be considered positive for the development of depression.
Time Frame
Baseline, Week 2, Week 6, Month 3, and Month 6
Title
Mean Change from Baseline in Impulsiveness Scores on the Barratt Impulsiveness Scale (BIS-11)
Description
The score of the BIS-11 will be evaluated across sessions and elevated scores indicate greater impulsivity and risk-taking behavior. The scale involves 30 questions with values from 1-4. Overall scores range from 30-120.
Time Frame
Baseline, Week 2, Week 6, Month 3, and Month 6
Title
Mean Change from Baseline in Neuropsychiatric Inventory (NPI)
Description
The NPI assesses frequency, change in severity, and distress over 12 neuropsychiatric domains as evaluated by the caregiver. We will look for a significant score reduction in any domain of the NPI.
Time Frame
Baseline, Week 2, Week 6, Month 3, and Month 6
Title
Mean Change from Baseline in Movement Scores on Part III of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS)
Description
Part III of the MDS-UPDRS consists of 18 areas of motor assessments to assess severity of symptoms. Each score is rated in terms of severity from 0-4, with higher scores indicating higher severity of symptoms. A composite score will be evaluated for changes from baseline.
Time Frame
Baseline, Week 2, Week 6, Month 3, and Month 6
Title
Mean Change from Baseline in Cognitive Performance Scores on the Montreal Cognitive Assessment - Blind (MoCA)
Description
This will be collected via telephone calls. The MoCA-Blind has been validated for telephone administration. We will re-evaluate MoCA-Blind scores during telephone monitoring to assess any changes to cognitive ability. A total score of less than 15 out of a possible 22 indicates greater than mild cognitive impairment.
Time Frame
Baseline, Hour 24, Week 1, Month 1, Month 2, Month 4, and Month 5
Title
Mean Change from Baseline in Depression Scores on the CES-D Short Version (CES-D-R10)
Description
This will be collected via telephone calls. Patients will be given an unmarked form with questions and will be able to follow along the telephone conversation and answer each question (0-4 severity rating scale) for 10 questions focused on patient affect. A total score greater than 10 (out of 30) indicates the development of depression symptoms.
Time Frame
Baseline, Hour 24, Week 1, Month 1, Month 2, Month 4, and Month 5
Title
Mean Change from Baseline in Motor and Non-Motor Aspects of Daily Living Scores on Parts I and II of the MDS-UPDRS
Description
This will be collected via telephone calls. Patients will be asked questions relating to motor and non-motor aspects of daily living and to rate the severity of their symptoms on a scale from 0-4, with higher scores indicating higher severity of symptoms. We will assess for changes in the composite score from baseline.
Time Frame
Baseline, Hour 24, Week 1, Month 1, Month 2, Month 4, and Month 5
Secondary Outcome Measure Information:
Title
Mean Change from Baseline in Decision-Making Scores on Probabilistic Gambling Task
Description
A patient-specific measure of risk attitude during a gambling task. We will estimate indifference points (win probability at which risky choice is chosen 50% of the time) at each time point and compare to those points during baseline performance on the task.
Time Frame
Baseline, Minute 30, Week 2, Week 6, Month 3, and Month 6
Title
Mean Change from Baseline in Inter-Temporal Choice Scores on a Temporal Discounting Task
Description
A patient-specific measure of risk attitude during a temporal preferences task. We will examine the area under the curve of the empirical discount functions of 'larger later' rewards and 'smaller sooner' rewards. Smaller values indicate increased preference for smaller sooner over larger later rewards. Scores will be compared to baseline performance on the task.
Time Frame
Baseline, Minute 30, Week 2, Week 6, Month 3, and Month 6
Title
Mean Change from Baseline in Verbal Fluency Scores on Word Generation Task
Description
The average number of words generated in a 1-minute time frame.
Time Frame
Baseline, Minute 30, Week 2, Week 6, Month 3, and Month 6

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Individuals who are 18 years and older Individuals with idiopathic Parkinson's Disease who previously underwent implantation with the Boston Scientific VerciseTM DBS system Individuals who have been implanted with the Boston Scientific VerciseTM DBS system for at least 3 months Individuals diagnosed with advanced PD who had bilateral dorsal subthalamic nucleus DBS surgery, as standard of care for motor improvement, with distal contacts of the electrodes implanted into the ventral STN Exclusion Criteria: Individuals unable to provide consent and/or lack capacity to consent Individuals diagnosed with any cognitive or physical impairments that would limit their ability to participate in the cognitive testing Individuals who score below 15 on the Montreal Cognitive Assessment Test-Blind Individuals who score above 20 on the Center for Epidemiologic Studies Depression Scale Pregnant women (note: pregnant women are not candidates for DBS surgery), and prisoners Non-English speaking individuals. Cognitive tasks will only be conducted in English.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kiarash Shahlaie, MD, PhD
Phone
916-703-5505
Email
krshahlaie@ucdavis.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Janice Wang-Polagruto, PhD, CCRP
Phone
916-551-3244
Email
jfwang@ucdavis.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kiarash Shahlaie, MD, PhD
Organizational Affiliation
University of California, Davis
Official's Role
Principal Investigator
Facility Information:
Facility Name
UC Davis Health
City
Sacramento
State/Province
California
ZIP/Postal Code
95817
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jessica Beatty, MS
Phone
916-734-0901
Email
jabeatty@ucdavis.edu
First Name & Middle Initial & Last Name & Degree
Janice Wang-Polagruto, PhD, CCRP
Phone
916-551-3244
Email
jfwang@ucdavis.edu

12. IPD Sharing Statement

Plan to Share IPD
No
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Dual Frequency Stimulation in Parkinson's Disease

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