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iTBS Study for Depression in Patients With Multiple Sclerosis

Primary Purpose

Multiple Sclerosis, Depression, Anxiety

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
intermittent theta burst stimulation using a MagPro X100
sham intermittent theta burst stimulation using a MagPro X100
Sponsored by
Third Affiliated Hospital, Sun Yat-Sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis focused on measuring Multiple Sclerosis, Depression, Transcranial Magnetic Stimulation

Eligibility Criteria

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

Inclusion Criteria:

  • 1) Age 18 to 65
  • 2) Male and female patients with clinically definite MS according to 2017 McDonald criteria
  • 3) EDSS 0 to 6
  • 4) Score between 11 and 30 on the Montgomery-Asberg Depression Rating Scale (MADRS) and stable antidepressants therapy > 1 months before enrollment and during the follow-up period
  • 5) Informed consent of patients

Exclusion Criteria:

  • 1) History of seizures (personal or family)
  • 2) Comedication with neuroleptics or tricyclic antidepressants
  • 3) bipolar disorder
  • 4) Presence of other diseases of the nervous system (history of stroke, brain injury, brain tumor, increased intracranial pressure)
  • 5) Significant neurologic, psychiatric, cardiovascular, hepatic, renal, gastrointestinal, metabolic, or other systemic comorbidities.
  • 6) History of drug or alcohol abuse
  • 7) Cardiac pacemakers
  • 8) Metal implants in the head
  • 9) Pregnancy

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Sham Comparator

    Arm Label

    iTBS stimulation

    sham iTBS stimulation

    Arm Description

    iTBS stimulation to left dorsolateral prefrontal cortex (DLPFC), twice daily, 10 days

    sham iTBS stimulation to left dorsolateral prefrontal cortex (DLPFC), twice daily, 10 days

    Outcomes

    Primary Outcome Measures

    Change in Montgomery-Asberg Depression Rating Scale (MADRS)
    The MADRS is a 0-60 point scale to measure depression severity with a higher number indicating more severe depression. A score of 0-6 indicates symptoms absent, 7-19 indicates mild depression, 20-34 moderate, and > 34 severe.

    Secondary Outcome Measures

    Presence and changes in severity of side effects
    Adverse events will be assessed by the physician from Department of Neurology weekly.
    Change in Beck Depressive Inventory (BDI)
    BDI is a widely utilized to assess depression in MS patients. It is a 21-item self-reporting questionnaire for evaluating the severity of depression. The score range is 0-63 with higher scores indicating higher intensity.
    Change in 21-item Beck's Anxiety Inventory (BAI)
    BAI is a self-report test for measuring anxiety severity and level. It contains 21 multiple-choice questions. The score range is 0-63 with higher scores indicating higher intensity.
    Change in Fatigue Severity Scale (FSS)
    The FSS is a 9-item scale which measure the severity of fatigue and its effect on an individual's daily living and social participation. The total score ranges from 9 to 63, with a higher score indicate greater fatigue severity.
    Change in Pittsburgh Sleep Quality Index (PSQI)
    PSQI is a self-rated questionnaire designed to evaluate overall sleep quality during the past month. Each of the questionnaire's 19 self-reported items belongs to one of seven subcategories: sleep quality, sleep latency, sleep duration, sleep efficiency, sleep disturbance, use of sleep medication, degree of daytime dysfunction.
    Change in Expand Disability Status Scale (EDSS)
    EDSS is a standardized method used to classify the severity and progression of multiple sclerosis. It provides a total score on a scale that ranges from 0 to 10.
    Change in Cortical silent period (CSP) duration
    CSP duration will be measured by Magventure X100 + option.
    Change in short-interval intracortical inhibition (SICI)
    SICI will be measured by Magventure X100 + option.
    Change in intracortical facilitation (ICF)
    ICF will be measured by Magventure X100 + option.
    Changes in long-interval intracortical inhibition (LICI)
    LICI will be measured by Magventure X100 + option.
    Change in slow-wave/fast-wave (theta/beta) ratio from resting-state electroencephalograph (EEG) recording
    Resting-state EEG will be recorded by Nicolet EEG system.
    Serum biomarker
    Serum biomarker such as BDNF, TNF-alpha, IL-1 beta, S100 beta will be examined before and after TMS treatment.

    Full Information

    First Posted
    August 2, 2020
    Last Updated
    November 21, 2020
    Sponsor
    Third Affiliated Hospital, Sun Yat-Sen University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04524039
    Brief Title
    iTBS Study for Depression in Patients With Multiple Sclerosis
    Official Title
    Intermittent Theta Burst Stimulation (iTBS) for the Treatment of Depression in Patients With Multiple Sclerosis: a Randomized Controlled Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    December 1, 2020 (Anticipated)
    Primary Completion Date
    September 1, 2022 (Anticipated)
    Study Completion Date
    December 31, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Third Affiliated Hospital, Sun Yat-Sen University

    4. Oversight

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

    5. Study Description

    Brief Summary
    Multiple sclerosis (MS) is a chronic and demyelinating disease of the central nervous system. It is one of the most common cause of neurological disability in young adults. Depression is a common symptom in MS patients, with lifetime prevalence rates going up to 50%. Depression not only reduces the response to treatment, delays the recovery of neurological function and social ability, but also significantly increases the risk of disability in patients with MS. Transcranial magnetic stimulation (TMS) is a non-invasive method of brain stimulation that is based on electromagnetic induction. Intermittent theta burst stimulation (TBS), a newer form of rTMS, delivers 600 pulses in just 3 min, versus 37.5 min for conventional rTMS, but it has been shown to produce similar effects in patient with treatment-resistant depression. To observe the effect and safety of iTBS on patients with MS and depression, we design a double-blind, randomized controlled study. Results of this research will inform on the efficiency of the TMS for the treatment of depression in MS patients, which will reduce the risk of disability and improve the quality of life.
    Detailed Description
    Multiple sclerosis (MS) is a chronic and demyelinating disease of the central nervous system. It is one of the most common cause of neurological disability in young adults. Depression is a common symptom in MS patients, with lifetime prevalence rates going up to 50%. Depression not only reduces the response to treatment, delays the recovery of neurological function and social ability, but also significantly increases the risk of disability in patients with MS. It is worth noting that depression remains widely underdiagnosed and untreated in MS patients. The investigators aim to treat the depression in MS patients using a non-invasive method, which will help improve life quality and reduce the risk of disability in patients. Transcranial magnetic stimulation (TMS) is a non-invasive method of brain stimulation that uses magnetic fields to stimulate nerve cells in brain. Repetitive TMS (rTMS) is usually applied in antidepressant-resistant depression. Furthermore, some clinical trials show that rTMS also significantly improve Parkinson's related depression and postpartum depression. Intermittent theta burst stimulation (TBS), a newer form of rTMS, delivers 600 pulses in just 3 min, versus 37.5 min for conventional rTMS, but it has been shown to produce similar effects in patient with treatment-resistant depression. In this study, thirty patients who meet the criteria will be included. They will then be randomly assigned into the SHAM or iTBS group for the study intervention. Patients and outcome assessors will be masked to treatment allocation. SHAM or iTBS will be delivered to stimulate left dorsalateral prefrontal cortex (DLPFC). The protocol includes 600 pulses per session: triplet 50 Hz bursts, repeated at 5 Hz; 2 s on and 8 s off. Each patient will receive 2 sessions per day over a period of 10 days (total of 20 sessions). After the treatment phase, patients will be followed up once after two weeks. The presence and severity of side effects will be assessed by the physician from the Department of Neurology. Before and after the iTBS or SHAM intervention and after two weeks of follow-up, primary and secondary measurements will be performed. Results of this study will inform on the efficiency of the TMS for the treatment of depression in MS patients, which will reduce the risk of disability and improve the quality of life.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Multiple Sclerosis, Depression, Anxiety
    Keywords
    Multiple Sclerosis, Depression, Transcranial Magnetic Stimulation

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    iTBS stimulation
    Arm Type
    Experimental
    Arm Description
    iTBS stimulation to left dorsolateral prefrontal cortex (DLPFC), twice daily, 10 days
    Arm Title
    sham iTBS stimulation
    Arm Type
    Sham Comparator
    Arm Description
    sham iTBS stimulation to left dorsolateral prefrontal cortex (DLPFC), twice daily, 10 days
    Intervention Type
    Device
    Intervention Name(s)
    intermittent theta burst stimulation using a MagPro X100
    Intervention Description
    Patients randomized to receive iTBS in left dorsolateral prefrontal cortex, each treatment will consist of 600 stimuli (triplet 50 Hz bursts, repeated at 5 Hz; 2 s on and 8 s off; total duration of 3 min 12 s). Simulated iTBS will be administered using Magventure static cooling MCF-B65 coil.
    Intervention Type
    Device
    Intervention Name(s)
    sham intermittent theta burst stimulation using a MagPro X100
    Intervention Description
    Patients randomized to receive sham iTBS will undergo the same procedure to patients receiving real iTBS. Sham iTBS will be administered using Magventure static cooling MCF-P-B65 coil that shares the same mechanical outline and produces identical sound level to MCF-B65 coil without stimulating the cerebral cortex.
    Primary Outcome Measure Information:
    Title
    Change in Montgomery-Asberg Depression Rating Scale (MADRS)
    Description
    The MADRS is a 0-60 point scale to measure depression severity with a higher number indicating more severe depression. A score of 0-6 indicates symptoms absent, 7-19 indicates mild depression, 20-34 moderate, and > 34 severe.
    Time Frame
    0 (baseline), 10 days and 4 weeks
    Secondary Outcome Measure Information:
    Title
    Presence and changes in severity of side effects
    Description
    Adverse events will be assessed by the physician from Department of Neurology weekly.
    Time Frame
    0 (baseline), 10 days and 4 weeks
    Title
    Change in Beck Depressive Inventory (BDI)
    Description
    BDI is a widely utilized to assess depression in MS patients. It is a 21-item self-reporting questionnaire for evaluating the severity of depression. The score range is 0-63 with higher scores indicating higher intensity.
    Time Frame
    0 (baseline), 10 days and 4 weeks
    Title
    Change in 21-item Beck's Anxiety Inventory (BAI)
    Description
    BAI is a self-report test for measuring anxiety severity and level. It contains 21 multiple-choice questions. The score range is 0-63 with higher scores indicating higher intensity.
    Time Frame
    0 (baseline), 10 days and 4 weeks
    Title
    Change in Fatigue Severity Scale (FSS)
    Description
    The FSS is a 9-item scale which measure the severity of fatigue and its effect on an individual's daily living and social participation. The total score ranges from 9 to 63, with a higher score indicate greater fatigue severity.
    Time Frame
    0 (baseline), 10 days and 4 weeks
    Title
    Change in Pittsburgh Sleep Quality Index (PSQI)
    Description
    PSQI is a self-rated questionnaire designed to evaluate overall sleep quality during the past month. Each of the questionnaire's 19 self-reported items belongs to one of seven subcategories: sleep quality, sleep latency, sleep duration, sleep efficiency, sleep disturbance, use of sleep medication, degree of daytime dysfunction.
    Time Frame
    0 (baseline), 10 days and 4 weeks
    Title
    Change in Expand Disability Status Scale (EDSS)
    Description
    EDSS is a standardized method used to classify the severity and progression of multiple sclerosis. It provides a total score on a scale that ranges from 0 to 10.
    Time Frame
    0 (baseline), 10 days and 4 weeks
    Title
    Change in Cortical silent period (CSP) duration
    Description
    CSP duration will be measured by Magventure X100 + option.
    Time Frame
    0 (baseline), 10 days and 4 weeks
    Title
    Change in short-interval intracortical inhibition (SICI)
    Description
    SICI will be measured by Magventure X100 + option.
    Time Frame
    0 (baseline), 10 days and 4 weeks
    Title
    Change in intracortical facilitation (ICF)
    Description
    ICF will be measured by Magventure X100 + option.
    Time Frame
    0 (baseline), 10 days and 4 weeks
    Title
    Changes in long-interval intracortical inhibition (LICI)
    Description
    LICI will be measured by Magventure X100 + option.
    Time Frame
    0 (baseline), 10 days and 4 weeks
    Title
    Change in slow-wave/fast-wave (theta/beta) ratio from resting-state electroencephalograph (EEG) recording
    Description
    Resting-state EEG will be recorded by Nicolet EEG system.
    Time Frame
    0 (baseline), 10 days and 4 weeks
    Title
    Serum biomarker
    Description
    Serum biomarker such as BDNF, TNF-alpha, IL-1 beta, S100 beta will be examined before and after TMS treatment.
    Time Frame
    0 (baseline), 10 days

    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: 1) Age 18 to 65 2) Male and female patients with clinically definite MS according to 2017 McDonald criteria 3) EDSS 0 to 6 4) Score between 11 and 30 on the Montgomery-Asberg Depression Rating Scale (MADRS) and stable antidepressants therapy > 1 months before enrollment and during the follow-up period 5) Informed consent of patients Exclusion Criteria: 1) History of seizures (personal or family) 2) Comedication with neuroleptics or tricyclic antidepressants 3) bipolar disorder 4) Presence of other diseases of the nervous system (history of stroke, brain injury, brain tumor, increased intracranial pressure) 5) Significant neurologic, psychiatric, cardiovascular, hepatic, renal, gastrointestinal, metabolic, or other systemic comorbidities. 6) History of drug or alcohol abuse 7) Cardiac pacemakers 8) Metal implants in the head 9) Pregnancy
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Wei Qiu, MD/Ph.D
    Phone
    +8615899968330
    Email
    qiuwei120@vip.163.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Liqing Wang, MD/Ph.D
    Phone
    +86(20)85253088
    Email
    wanglq5@mail.sysu.edu.cn
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Wei Qiu, MD/Ph.D
    Organizational Affiliation
    Third Affiliated Hospital, Sun Yat-Sen University
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Liqing Wang, MD/Ph.D
    Organizational Affiliation
    Third Affiliated Hospital, Sun Yat-Sen University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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