search
Back to results

Investigating the Neural Mechanisms of Repetitive Brain Stimulation With Invasive and Noninvasive Electrophysiology in Humans

Primary Purpose

Major Depressive Disorder, Epilepsy

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Intracranial electrodes
TMS
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Major Depressive Disorder

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Men and women, ages 18 to 65 Medication-refractory epilepsy requiring phase II monitoring Must have intellectual capacity to ensure adequate comprehension of the study and potential risks involved in order to provide informed consent No current or history of major neurological disorders other than epilepsy Exclusion Criteria: Those with a contraindication for MRIs (e.g. implanted metal) Any unstable medical condition Neurological or uncontrolled medical disease Active substance abuse Currently pregnant or breastfeeding

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Active Comparator

    Active Comparator

    Sham Comparator

    Sham Comparator

    Arm Label

    TBS via direct electrical stimulation

    TBS via transcranial magnetic stimulation

    Sham TBS via direct electrical stimulation

    Sham TBS via transcranial magnetic stimulation

    Arm Description

    Outcomes

    Primary Outcome Measures

    TMS-iEEG change after one TBS session
    Change in evoked response measured after a single TBS session for active and sham, by resting state iEEG (intracranial EEG) and/or sEEG (stereo EEG).

    Secondary Outcome Measures

    ES-iEEG change after one TBS session
    Change in evoked response measured after a single TBS session for active and sham, by resting state iEEG and/or sEEG.
    ES-iEEG change between two sequential TBS sessions
    Change in single-pulse evoked response, or cortico-cortical evoked potentials (CCEPs), measured between two sequential TBS sessions, by resting state iEEG and/or sEEG.
    TMS-iEEG change between two sequential TBS sessions
    Change in single-pulse evoked response, or cortico-cortical evoked potentials (CCEPs), measured between two sequential TBS sessions, by resting state iEEG and/or sEEG.

    Full Information

    First Posted
    July 18, 2023
    Last Updated
    August 9, 2023
    Sponsor
    Stanford University
    Collaborators
    University of Iowa, Massachusetts General Hospital
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT05996900
    Brief Title
    Investigating the Neural Mechanisms of Repetitive Brain Stimulation With Invasive and Noninvasive Electrophysiology in Humans
    Official Title
    Investigating the Neural Mechanisms of Repetitive Brain Stimulation With Invasive and Noninvasive Electrophysiology in Humans
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 1, 2023 (Anticipated)
    Primary Completion Date
    January 1, 2027 (Anticipated)
    Study Completion Date
    July 1, 2028 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Stanford University
    Collaborators
    University of Iowa, Massachusetts General Hospital

    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.
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Transcranial magnetic stimulation (TMS) is an effective treatment for depression, but clinical outcome is suboptimal, partially because investigators are missing biologically-grounded brain markers which show that TMS is modifying activity at the intended target in the brain. The goal of this proposal is to characterize the key markers of the brain's response to repeated doses of TMS with high resolution using invasive brain recordings in humans, and relate these brain markers to noninvasive recordings. These markers will improve the understanding of TMS and can be used to optimize and enhance clinical efficacy for depression and other psychiatric disorders.
    Detailed Description
    Repetitive transcranial magnetic stimulation (rTMS) is an effective treatment for major depressive disorder, but remission rates are 20-40%, and ideal stimulation parameters are unknown. rTMS is thought to work by changing the synaptic strength of neurons. The ability of the brain to make these changes is referred to as plasticity. rTMS-induced changes are thought to build with successive treatment sessions, a process referred to as metaplasticity. While both plasticity and metaplasticity are well-established in single cell physiology, relevance to rTMS in humans remains unknown. To improve clinical efficacy, the investigators need to understand 1) the neural response to a single rTMS session (plasticity), 2) the neural response to repeated daily rTMS sessions (metaplasticity), and 3) whether computational models of plasticity based on single-cell physiology apply to human patients receiving rTMS for depression. Goals of the study are to 1) establish a detailed mechanistic understanding of the brain changes during current rTMS treatment; 2) identify clinically meaningful electrophysiological biomarkers for rTMS treatment; 3) establish a computational model to help predict both brain and clinical changes.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Major Depressive Disorder, Epilepsy

    7. Study Design

    Primary Purpose
    Basic Science
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    ParticipantOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    49 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    TBS via direct electrical stimulation
    Arm Type
    Active Comparator
    Arm Title
    TBS via transcranial magnetic stimulation
    Arm Type
    Active Comparator
    Arm Title
    Sham TBS via direct electrical stimulation
    Arm Type
    Sham Comparator
    Arm Title
    Sham TBS via transcranial magnetic stimulation
    Arm Type
    Sham Comparator
    Intervention Type
    Device
    Intervention Name(s)
    Intracranial electrodes
    Intervention Description
    Intracranial electrodes will be used for the delivery of invasive brain stimulation.
    Intervention Type
    Device
    Intervention Name(s)
    TMS
    Intervention Description
    TMS will be used for the delivery of noninvasive brain stimulation both before and after implantation electrode surgery.
    Primary Outcome Measure Information:
    Title
    TMS-iEEG change after one TBS session
    Description
    Change in evoked response measured after a single TBS session for active and sham, by resting state iEEG (intracranial EEG) and/or sEEG (stereo EEG).
    Time Frame
    45 minutes
    Secondary Outcome Measure Information:
    Title
    ES-iEEG change after one TBS session
    Description
    Change in evoked response measured after a single TBS session for active and sham, by resting state iEEG and/or sEEG.
    Time Frame
    45 minutes
    Title
    ES-iEEG change between two sequential TBS sessions
    Description
    Change in single-pulse evoked response, or cortico-cortical evoked potentials (CCEPs), measured between two sequential TBS sessions, by resting state iEEG and/or sEEG.
    Time Frame
    45 minutes
    Title
    TMS-iEEG change between two sequential TBS sessions
    Description
    Change in single-pulse evoked response, or cortico-cortical evoked potentials (CCEPs), measured between two sequential TBS sessions, by resting state iEEG and/or sEEG.
    Time Frame
    45 minutes

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Men and women, ages 18 to 65 Medication-refractory epilepsy requiring phase II monitoring Must have intellectual capacity to ensure adequate comprehension of the study and potential risks involved in order to provide informed consent No current or history of major neurological disorders other than epilepsy Exclusion Criteria: Those with a contraindication for MRIs (e.g. implanted metal) Any unstable medical condition Neurological or uncontrolled medical disease Active substance abuse Currently pregnant or breastfeeding
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Jade Truong
    Phone
    (408) 840-3313
    Email
    kellerlab@stanford.edu

    12. IPD Sharing Statement

    Learn more about this trial

    Investigating the Neural Mechanisms of Repetitive Brain Stimulation With Invasive and Noninvasive Electrophysiology in Humans

    We'll reach out to this number within 24 hrs