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Bilateral DLPC tDCS in Drug-resistant Migraine

Primary Purpose

Migraine

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Transcranial direct current stimulation (tDCS)
anti-CGRP-mAbs
Sponsored by
Clínica de Intervención en Neurociencias
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Migraine focused on measuring migraine, drug-resistant, tDCS, DLPC, Neuromodulation, anti CGRP

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: diagnosis of high-frequency and/or chronic migraines, according to the diagnostic criteria of the ICHD-III, failure to more than 3 preventive drugs stable pharmacological treatment (> 6 months without changes), absence of other neurological or medical pathological conditions, written informed consent. Exclusion Criteria: seizures significant cognitive impairment that prevents following orders and understanding instructions (Mini-Mental State Examination < 23) pregnancy aphasia or limitations in communication, metallic cranial implants another neurological or psychiatric pathology diagnosis of another type of migraine.

Sites / Locations

  • Clinica de Intervencion en Neurociencias

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Placebo Comparator

Active Comparator

Arm Label

Real tDCS

Sham tDCS

anti-CGRP

Arm Description

Patients will undergo real tDCS applied to both DLPC. Two daily sessions of 20 minutes each were administered (40 minutes a day in total), with a 5-minutes break in between, 5 days a week (Monday to Friday) and with 20 tDCS sessions in total for participant

Patients will undergo sham tDCS applied to both DLPC. Two daily sessions of 20 minutes each were administered (40 minutes a day in total), with a 5-minutes break in between, 5 days a week (Monday to Friday) and with 20 tDCS sessions in total for participant

Patients will undergo anti-CGRP treatment

Outcomes

Primary Outcome Measures

Migraine attacks monthly frequency
Patients will report migraine monthly frequency for the 3 different time-points
Headache Impact Test (HIT-6) score
HIT-6 is a tool used to measure the impact headaches have on patient's ability to function on the job, at school, at home and in social situations.
Pain killer drugs monthly taken
Patients will report pain-killer drugs taken during a month for the 3 different time-points

Secondary Outcome Measures

The Pittsburgh Sleep Quality Index (PSQI)
PSQI is a self-report questionnaire that assesses sleep quality over a 1-month time interval. The measure consists of 19 individual items, creating 7 components that produce one global score, and takes 5-10 minutes to complete.
Brief Symptom Inventory (BSI)
The Brief Symptom Inventory (BSI) consists of 53 items covering nine symptom dimensions: Somatization, Obsession-Compulsion, Interpersonal Sensitivity, Depression, Anxiety, Hostility, Phobic anxiety, Paranoid ideation and Psychoticism; and three global indices of distress: Global Severity Index, Positive Symptom Distress Index, and Positive Symptom Total. The global indices measure current or past level of symptomatology, intensity of symptoms, and number of reported symptoms, respectively.

Full Information

First Posted
September 29, 2023
Last Updated
October 15, 2023
Sponsor
Clínica de Intervención en Neurociencias
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1. Study Identification

Unique Protocol Identification Number
NCT06079801
Brief Title
Bilateral DLPC tDCS in Drug-resistant Migraine
Official Title
Bilateral DLPC tDCS: a New Potential Neuromodulatory Strategy in Drug-resistant Migraine
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
October 1, 2021 (Actual)
Primary Completion Date
April 30, 2023 (Actual)
Study Completion Date
August 31, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Clínica de Intervención en Neurociencias

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this clinical trial is to study and describe the effects of bilateral tDCS applied to dorso-lateral-prefrontal cortex (DLPC) in patients with drug-resistant migraine in terms of reduction in frequency of pain, impact of pain in daily life, quality of sleep and psychological measures. We finally planned to include high frequency and chronic migraine patients. The main questions it aims to answer are: Will bilateral DLPC tDCS be feasible, well tolerated and safe in drug resistant migraine patients? Will bilateral DLPC tDCS be effective in reducing pain frequency, intensity and its impact in daily life activities? Will bilateral DLPC tDCS be effective in ameliorating sleep and psychological associated symptoms? Will bilateral DLPC tDCS be such effective in reducing pain frequency, intensity and its impact in daily life activities as anti-CGRP treatments? Participants will undergo 2 tDCS sessions daily for 2 consecutive weeks. Patients will be blinded to treatment and will be divided in two groups (real vs placebo). A third group of patients, age-matched to the other two, will undergo anti-CGRP treatment. Patients will be asked to complete Patient-Reported Outcomes (PROMs) scales at baseline, one week after the end of the treatment and at 6 months after the end of the treatment. Researchers (blinded to the treatment) will compare the group that underwent real tDCS treatment vs the one that underwent placebo tDCS vs the one that underwent anti-CGRP drugs to see if bilateral DLPC tDCS is effective in reducing migraine frequency, intensity and impact and if bilateral DLPC tDCS is such effective as anti-CGRP treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Migraine
Keywords
migraine, drug-resistant, tDCS, DLPC, Neuromodulation, anti CGRP

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
36 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Real tDCS
Arm Type
Experimental
Arm Description
Patients will undergo real tDCS applied to both DLPC. Two daily sessions of 20 minutes each were administered (40 minutes a day in total), with a 5-minutes break in between, 5 days a week (Monday to Friday) and with 20 tDCS sessions in total for participant
Arm Title
Sham tDCS
Arm Type
Placebo Comparator
Arm Description
Patients will undergo sham tDCS applied to both DLPC. Two daily sessions of 20 minutes each were administered (40 minutes a day in total), with a 5-minutes break in between, 5 days a week (Monday to Friday) and with 20 tDCS sessions in total for participant
Arm Title
anti-CGRP
Arm Type
Active Comparator
Arm Description
Patients will undergo anti-CGRP treatment
Intervention Type
Device
Intervention Name(s)
Transcranial direct current stimulation (tDCS)
Intervention Description
TDCS was delivered by a DC-Stimulator (Newronika, Italy) over both DLPC. The electrodes (35 cm2) were soaked in 0.9% NaCl. The anode was positioned on the left dorsolateral prefrontal cortex and the cathode on the right dorsolateral prefrontal cortex.
Intervention Type
Drug
Intervention Name(s)
anti-CGRP-mAbs
Intervention Description
CGRP-mAbs have been the first target-driven treatment to be approved for migraine prevention. Their efficacy and safety have been demonstrated in randomized controlled trials (RCT) as well as, in real-world evidence (RWE) studies
Primary Outcome Measure Information:
Title
Migraine attacks monthly frequency
Description
Patients will report migraine monthly frequency for the 3 different time-points
Time Frame
baseline, 2 weeks after the end of the treatment, 6 months
Title
Headache Impact Test (HIT-6) score
Description
HIT-6 is a tool used to measure the impact headaches have on patient's ability to function on the job, at school, at home and in social situations.
Time Frame
baseline, 2 weeks after the end of the treatment, 6 months
Title
Pain killer drugs monthly taken
Description
Patients will report pain-killer drugs taken during a month for the 3 different time-points
Time Frame
baseline, 2 weeks after the end of the treatment, 6 months
Secondary Outcome Measure Information:
Title
The Pittsburgh Sleep Quality Index (PSQI)
Description
PSQI is a self-report questionnaire that assesses sleep quality over a 1-month time interval. The measure consists of 19 individual items, creating 7 components that produce one global score, and takes 5-10 minutes to complete.
Time Frame
baseline, 2 weeks after the end of the treatment, 6 months
Title
Brief Symptom Inventory (BSI)
Description
The Brief Symptom Inventory (BSI) consists of 53 items covering nine symptom dimensions: Somatization, Obsession-Compulsion, Interpersonal Sensitivity, Depression, Anxiety, Hostility, Phobic anxiety, Paranoid ideation and Psychoticism; and three global indices of distress: Global Severity Index, Positive Symptom Distress Index, and Positive Symptom Total. The global indices measure current or past level of symptomatology, intensity of symptoms, and number of reported symptoms, respectively.
Time Frame
baseline, 2 weeks after the end of the treatment, 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diagnosis of high-frequency and/or chronic migraines, according to the diagnostic criteria of the ICHD-III, failure to more than 3 preventive drugs stable pharmacological treatment (> 6 months without changes), absence of other neurological or medical pathological conditions, written informed consent. Exclusion Criteria: seizures significant cognitive impairment that prevents following orders and understanding instructions (Mini-Mental State Examination < 23) pregnancy aphasia or limitations in communication, metallic cranial implants another neurological or psychiatric pathology diagnosis of another type of migraine.
Facility Information:
Facility Name
Clinica de Intervencion en Neurociencias
City
Talavera De La Reina
State/Province
Toledo
ZIP/Postal Code
45600
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
We will publish results of the study and we will provide more information for reviewers if required

Learn more about this trial

Bilateral DLPC tDCS in Drug-resistant Migraine

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