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CompletedNCT03414203NEUROMIGUpdated Aug 28, 2019

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

An interventional study of tDCS in Chronic Migraine, sponsored by Federal University of Paraíba. Completed at 1 site in Brazil. Open to female participants aged 20 Years to 45 Years. Per ClinicalTrials.gov, last updated 2019-08-28.

Sponsored by Federal University of Paraíba · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled Aug 2017, registered Jan 2018).

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Phase
Not applicable
Study type
Interventional
Enrollment
31
Allocation
Randomized
Ages
20 Years to 45 Years
Sex
Female
01

Where this study stands

Counted across the records on this site · 2026-11-14

Among 25 studies in Migraine Disorders with a site in Brazil — 3 open to participants now, 4 under way, none of them phase 3. Migraine Disorders · Brazil.

Enrollment
16th of 23
31 · median 60
Started
2017
the only one that year
No phase
11 of 25
2 open now
Registered
16th of 25
by date
Lead sponsor
4 of 25
Federal University of Paraíba

Among the 25 studies in Migraine Disorders with a site in Brazil, this one is the 16th largest by enrollment of the 23 interventional ones that give a count, is the only one that started in 2017, is one of 11 with no phase, and was the 16th registered.

Migraine Disorders

1,657 studies on the registry are indexed under Migraine Disorders; 339 are open to participants now.

Browse Migraine Disorders studies →

Open to participants now

3 of the 25 studies in Migraine Disorders with a site in Brazil are open now. Recruiting first, the newest first:

All 3 open studies →

A study can be open while its sites in Brazil have not opened yet or have stopped. Only those recruiting at a site in Brazil →

Who these studies take

Of the 217 Migraine Disorders studies recruiting now, 66 (30%) set no upper age limit and 136 (63%) stop at 75 or younger; 44 take children under 18; 37 take healthy volunteers.

This study: 20 Years to 45 Years · female · no healthy volunteers.

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02

Study summary

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

Read the 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.

03

Conditions studied

  • Chronic Migraine

Keywords

  • Transcranial Direct Current Stimulation
  • Migraine Disorders
  • Cognitive Symptoms
04

Who can participate

Ages eligible
20 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

Exclusion criteria

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
31 participants (actual)

Study arms

  • Active comparator
    active tDCS

    Active tDCS for 15 minutes for 10 days over 2 weeks. Intensity: 2 milliampere. Placement: anode - left DLPFC; cathode - right supraorbital region

    Other: tDCS

  • Experimental
    active tDCS with interval

    Active tDCS for 15 minutes, interval of 20 minutes and more 15 minutes for 10 days over 2 weeks. Intensity: 2 milliampere. Placement: anode - left DLPFC; cathode - right supraorbital region

    Other: tDCS

  • Sham comparator
    sham tDCS

    Sham tDCS for 15 minutes for 10 days over 2 weeks. The stimulation is non-active. Placement: anode - left DLPFC; cathode - right supraorbital region

    Other: tDCS

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.

06

What researchers measure

Primary outcomes

  1. Migraine Disability Assessment - MIDAS

    Change in perform activities of daily living associate to migraine assessed on the Migraine Disability Assessment - MIDAS.

    Time frame: "before treatment", "after treatment - up to 2 weeks " and "up to 1 month after the last day of treatment"

Secondary outcomes

  1. Headache Impact Test - HIT-6

    Change in quality of life associate to migraine assessed on the Headache Impact Test-6 (HIT-6)

    Time frame: "before treatment", "after treatment - up to 2 weeks " and "up to 1 month after the last day of treatment"

  2. Wechsler Intelligence Scale Letters

    Change in cognitive ability assessed on the Wechsler Adult Intelligence Scale Letters

    Time frame: "before treatment", "after treatment - up to 2 weeks " and "up to 1 month after the last day of treatment"

  3. Wechsler Intelligence Scale Numbers Test

    Change in cognitive ability assessed on the Wechsler Adult Intelligence Scale Numbers Test

    Time frame: "before treatment", "after treatment - up to 2 weeks " and "up to 1 month after the last day of treatment"

  4. Hayling's Test Hayling's Test

    Change in operational memory assessed on the Hayling's Test Evaluate operational memory

    Time frame: "before treatment", "after treatment - up to 2 weeks " and "up to 1 month after the last day of treatment"

  5. Trail Making Test part B

    Change in executive functions assessed on the Trail Making Test part B

    Time frame: "before treatment", "after treatment - up to 2 weeks " and "up to 1 month after the last day of treatment"

  6. Salthouse Visual Patterns and Lyrics

    Change in visual processing speed assessed on the Salthouse Visual Patterns and Lyrics

    Time frame: "before treatment", "after treatment - up to 2 weeks " and "up to 1 month after the last day of treatment"

  7. Nine Hole Peg Test

    Change in the motor processing speed assessed on the Nine Hole Peg Test

    Time frame: "before treatment", "after treatment - up to 2 weeks " and "up to 1 month after the last day of treatment"

  8. Paced Auditory Serial Addition Task

    Change in selective attention assessed on the Paced Auditory Serial Addition Task

    Time frame: "before treatment", "after treatment - up to 2 weeks " and "up to 1 month after the last day of treatment"

  9. Concentrated Attention Test

    Change in selective attention assessed on the Concentrated Attention Test

    Time frame: "before treatment", "after treatment - up to 2 weeks " and "up to 1 month after the last day of treatment"

  10. Visual Attention Test (Attention Matrices)

    Change in selective attention assessed on the Visual Attention Test (Attention Matrices)

    Time frame: "before treatment", "after treatment - up to 2 weeks " and "up to 1 month after the last day of treatment"

  11. Montreal Cognitive Assessment

    Change in cognition assessed on the Montreal Cognitive Assessment

    Time frame: "before treatment", "after treatment - up to 2 weeks " and "up to 1 month after the last day of treatment"

  12. Side Effects Questionnaire

    adverse effects assessment

    Time frame: "every day for up to 2 weeks"

07

Study locations

1 site
  • Federal University of Paraiba
    João Pessoa, Paraiba, Brazil
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Aug 2017 to primary completion in Feb 2018, 5 months.

Of 309 non-industry interventional studies with no phase under Migraine Disorders, half reached primary completion within 17 months of starting (the median), counting those still running; a quarter within 8 and three quarters within 36. This study's 5 months is below that.

Counting every sponsor, half of 358 studies reached it within 15 months; a quarter within 7 and three quarters within 34.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 10, 2018
First posted
Jan 29, 2018
StartActual
Aug 14, 2017
Primary completionActual
Feb 5, 2018
CompletionActual
Feb 16, 2018
Last update
Aug 28, 2019
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 28, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03414203
Lead sponsor
Federal University of Paraíba
Responsible party
Renata Emanuela Lyra de Brito Aranha (researcher, Federal University of Paraíba) — Principal investigator
First posted
Jan 29, 2018
Start date
Aug 14, 2017
Primary completion
Feb 5, 2018
Completion
Feb 16, 2018
Last update
Aug 28, 2019

Study contacts

Renata Aranha
principal investigator · Federal University of Paraiba

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2019. You cannot join it, but the record below documents what was studied.

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