Skip to content

Comparison Between Transcranial Stimulation Protocols With Continuous Current in the Chronic Migraine

Comparison Between Stimulation Transcranial Protocols With Continuous Current in the Chronic Migraine: Clinical Trial, Triple-blind, Placebo-controlled

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03414203
Acronym
NEUROMIG
Enrollment
31
Registered
2018-01-29
Start date
2017-08-14
Completion date
2018-02-16
Last updated
2019-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Migraine

Keywords

Transcranial Direct Current Stimulation, Migraine Disorders, Cognitive Symptoms

Brief summary

This study aims to compare the effects of transcranial direct current stimulation on the clinical and cognitive function in patients with chronic migraine.

Detailed description

The patients will be randomized into 1 of 3 groups: active tDCS for 15 minutes, active tDCS for 15 minutes, with an interval of 20 minutes and more 15 minutes os stimulation, sham tDCS for 15 minutes. The tDCS will be applied for 10 days over 2 weeks.

Interventions

OTHERtDCS

Transcranial Current Stimulation equipment consists of an ammeter (measured with current intensity), a potentiometer (voltage controller between the electrodes), a generator (two 9-volt batteries) and two electrodes (anode and cathode). The direct low-amplitude currents released by the electrodes reach the cortex and modify the neuronal potentials.

Sponsors

Federal University of Paraíba
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

The patients will be randomized into 1 of 3 groups: group A: active tDCS for 15 minutes, group B: active tDCS for 15 minutes, with an interval of 20 minutes and group C: more 15 minutes os stimulation, sham tDCS for 15 minutes.

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* females * clinical diagnosis of chronic migraine according to the International Classification of Headaches Disorders (ICHD-3 beta).

Exclusion criteria

* headache attributable to some pathological condition, associated neurologic or neuropsychiatric disease * use of central nervous system modulating drugs * pregnancy * metallic head implants * use of a cardiac pacemaker

Design outcomes

Primary

MeasureTime frameDescription
Migraine Disability Assessment - MIDASbefore treatment, after treatment - up to 2 weeks and up to 1 month after the last day of treatmentChange in perform activities of daily living associate to migraine assessed on the Migraine Disability Assessment - MIDAS.

Secondary

MeasureTime frameDescription
Wechsler Intelligence Scale Lettersbefore treatment, after treatment - up to 2 weeks and up to 1 month after the last day of treatmentChange in cognitive ability assessed on the Wechsler Adult Intelligence Scale Letters
Wechsler Intelligence Scale Numbers Testbefore treatment, after treatment - up to 2 weeks and up to 1 month after the last day of treatmentChange in cognitive ability assessed on the Wechsler Adult Intelligence Scale Numbers Test
Hayling's Test Hayling's Testbefore treatment, after treatment - up to 2 weeks and up to 1 month after the last day of treatmentChange in operational memory assessed on the Hayling's Test Evaluate operational memory
Trail Making Test part Bbefore treatment, after treatment - up to 2 weeks and up to 1 month after the last day of treatmentChange in executive functions assessed on the Trail Making Test part B
Salthouse Visual Patterns and Lyricsbefore treatment, after treatment - up to 2 weeks and up to 1 month after the last day of treatmentChange in visual processing speed assessed on the Salthouse Visual Patterns and Lyrics
Headache Impact Test - HIT-6before treatment, after treatment - up to 2 weeks and up to 1 month after the last day of treatmentChange in quality of life associate to migraine assessed on the Headache Impact Test-6 (HIT-6)
Paced Auditory Serial Addition Taskbefore treatment, after treatment - up to 2 weeks and up to 1 month after the last day of treatmentChange in selective attention assessed on the Paced Auditory Serial Addition Task
Concentrated Attention Testbefore treatment, after treatment - up to 2 weeks and up to 1 month after the last day of treatmentChange in selective attention assessed on the Concentrated Attention Test
Visual Attention Test (Attention Matrices)before treatment, after treatment - up to 2 weeks and up to 1 month after the last day of treatmentChange in selective attention assessed on the Visual Attention Test (Attention Matrices)
Montreal Cognitive Assessmentbefore treatment, after treatment - up to 2 weeks and up to 1 month after the last day of treatmentChange in cognition assessed on the Montreal Cognitive Assessment
Side Effects Questionnaireevery day for up to 2 weeksadverse effects assessment
Nine Hole Peg Testbefore treatment, after treatment - up to 2 weeks and up to 1 month after the last day of treatmentChange in the motor processing speed assessed on the Nine Hole Peg Test

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026