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
About this trial
This is an interventional prevention trial for Migraine
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
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
NCT ID
NCT03900611
First Posted
April 2, 2019
Last Updated
January 26, 2021
Sponsor
Taipei Veterans General Hospital, Taiwan
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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