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Peripheral Electrical Stimulation for Migraine Prevention

Primary Purpose

Migraine

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
peripheral electrical stimulation
Sponsored by
Taipei Veterans General Hospital, Taiwan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Migraine

Eligibility Criteria

20 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Migraine:

    1. Diagnosed as migraine by International Classification of Headache Disorder (ICHD-III) criteria
    2. onset before 50 years old
    3. 20-65 yrs.
    4. 4 or more migraine days per month in average
  • Healthy control:

    1. devoid of any systemic or neurological diseases

Exclusion Criteria:

  1. history of major systemic illness, including uncontrolled hypertension, diabetes, chronic renal insufficiency, autoimmune diseases or malignancies
  2. history of neurological disorders which might affect sensation such as previous stroke or peripheral neuropathy
  3. pregnancy or lactation
  4. epilepsy
  5. moderate depressed (BDI>20)
  6. using prophylactics for migraine
  7. other remote electrical stimulation contraindications, such as open wound, sensory impairment, metal implant
  8. other transcranial magnetic stimulation contraindications, such as, high intracranial pressure, cochlear implant, cranial metal implant
  9. other magnetic resonance imaging contraindications, such as, pacemaker, stent, metal implant, claustrophobia

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Sham Comparator

    No Intervention

    Arm Label

    Active stimulation

    Sham stimulation

    healthy control

    Arm Description

    Outcomes

    Primary Outcome Measures

    change in migraine or headache days of a month in average
    change in migraine or headache days of a month in average
    responder rate
    responder rate (50% pain reduction from baseline)

    Secondary Outcome Measures

    change in moderate to severe headache days of a month in average
    acute headache medication use
    Beck Depression Inventory
    modified Migraine Disability Scale
    This modified Migraine Disability Scale assesses the migraine related disability in the past 1 month. The total score will be compared and the lower score stands for better outcome.
    Patient/Clinical Global Impression of Change
    Patient/Clinical Global Impression of Change (PGIC/CGIC) are 7-point scales to assess the improvement by patients themselves and by their clinicians.
    Sensory threshold change after treatment
    Using quantitative sensory testing (QST) to evaluate the sensory threshold before and after treatment
    EEG change after treatment (1) Linear analysis of EEG before and after treatment
    power spectal density change of EEG before and after treatment
    EEG change after treatment (2) Nonlinear analysis of EEG before and after treatment
    functional connectivity change of EEG before and after treatment
    fMRI change after treatment
    functional connectivity change of fMRI before and after treatment
    MRI change after treatment
    VBM changes of MRI before and after treatment

    Full Information

    First Posted
    April 2, 2019
    Last Updated
    January 26, 2021
    Sponsor
    Taipei Veterans General Hospital, Taiwan
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03900611
    Brief Title
    Peripheral Electrical Stimulation for Migraine Prevention
    Official Title
    To Investigate the Effects of Peripheral Electrical Stimulation on Cortical Imagining, Electrophysiology and Clinical Profile in Patients With Migraine
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    February 1, 2021 (Anticipated)
    Primary Completion Date
    June 30, 2022 (Anticipated)
    Study Completion Date
    December 31, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Taipei Veterans General Hospital, Taiwan

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    Migraine is a common and disabling disease that affects more than 10% of the population worldwide. The prevalence of migraine in Taiwan is around 9.1%. The migraineurs missed 2 workdays due to migraine per year, that is 3.7 million estimated missed workdays in total and an estimated cost of 4.6 billion New Taiwan dollars. In addition, some migraineurs have poor response to the medications or suffer from adverse effects, and may further develop medication-overuse headache. Therefore, in recent years, efforts have been made to develop non-medication treatments, and the number of studies using neuromodulation as an intervention has increased dramatically. Among them, peripheral electrical stimulation has long been a routine treatment for pain in the clinic, and research has also shown its good evidence. In addition, recent studies have shown that peripheral electrical stimulation can also alter the cortical activities. Compared with the proximal brain stimulation, the remote electrical stimulation is safer, more convenient, less expensive and suitable for home use. To date, only one research had focused on the immediate anesthetic effect of remote electrical stimulation whereas the research for migraine prevention is still absent. Therefore, we expect to utilize a more remote electrical stimulation than trigeminal nerve electrical stimulation, which is the commonly used research method nowadays, as an interventional model. In three years, we will recruit 80 migraineurs along with 40 healthy controls and investigate the effects of 8-week home-based remote electrical stimulation on the prevention of migraine and the mechanisms using brain imaging, electrophysiological and biochemical examinations. We also aim to identify the predictors of the responders to remote electrical stimulation. If the effects of remote electrical stimulation are confirmed, as a non-drug neuromodulation management with features of non-invasive, low adverse effects and high accessibility, it will greatly lower the cost of social health care and better improve the quality of life and clinical status of the migraineurs.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Migraine

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Active stimulation
    Arm Type
    Experimental
    Arm Title
    Sham stimulation
    Arm Type
    Sham Comparator
    Arm Title
    healthy control
    Arm Type
    No Intervention
    Intervention Type
    Device
    Intervention Name(s)
    peripheral electrical stimulation
    Intervention Description
    The subjects will undergo 8-week home-based peripheral electrical simulation on the median nerve. The peripheral electrical simulation will be performed once a day for 30 minutes. The stimulation will be active or sham depend on the group assignment.
    Primary Outcome Measure Information:
    Title
    change in migraine or headache days of a month in average
    Description
    change in migraine or headache days of a month in average
    Time Frame
    2 months
    Title
    responder rate
    Description
    responder rate (50% pain reduction from baseline)
    Time Frame
    2 months
    Secondary Outcome Measure Information:
    Title
    change in moderate to severe headache days of a month in average
    Time Frame
    2 months
    Title
    acute headache medication use
    Time Frame
    2 months
    Title
    Beck Depression Inventory
    Time Frame
    2 months
    Title
    modified Migraine Disability Scale
    Description
    This modified Migraine Disability Scale assesses the migraine related disability in the past 1 month. The total score will be compared and the lower score stands for better outcome.
    Time Frame
    2 months
    Title
    Patient/Clinical Global Impression of Change
    Description
    Patient/Clinical Global Impression of Change (PGIC/CGIC) are 7-point scales to assess the improvement by patients themselves and by their clinicians.
    Time Frame
    2 months
    Title
    Sensory threshold change after treatment
    Description
    Using quantitative sensory testing (QST) to evaluate the sensory threshold before and after treatment
    Time Frame
    2 months
    Title
    EEG change after treatment (1) Linear analysis of EEG before and after treatment
    Description
    power spectal density change of EEG before and after treatment
    Time Frame
    2 months
    Title
    EEG change after treatment (2) Nonlinear analysis of EEG before and after treatment
    Description
    functional connectivity change of EEG before and after treatment
    Time Frame
    2 months
    Title
    fMRI change after treatment
    Description
    functional connectivity change of fMRI before and after treatment
    Time Frame
    2 months
    Title
    MRI change after treatment
    Description
    VBM changes of MRI before and after treatment
    Time Frame
    2 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Migraine: Diagnosed as migraine by International Classification of Headache Disorder (ICHD-III) criteria onset before 50 years old 20-65 yrs. 4 or more migraine days per month in average Healthy control: devoid of any systemic or neurological diseases Exclusion Criteria: history of major systemic illness, including uncontrolled hypertension, diabetes, chronic renal insufficiency, autoimmune diseases or malignancies history of neurological disorders which might affect sensation such as previous stroke or peripheral neuropathy pregnancy or lactation epilepsy moderate depressed (BDI>20) using prophylactics for migraine other remote electrical stimulation contraindications, such as open wound, sensory impairment, metal implant other transcranial magnetic stimulation contraindications, such as, high intracranial pressure, cochlear implant, cranial metal implant other magnetic resonance imaging contraindications, such as, pacemaker, stent, metal implant, claustrophobia

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

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    Peripheral Electrical Stimulation for Migraine Prevention

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