Bilateral DLPC tDCS in Drug-resistant Migraine
- Conditions
- Migraine
- Interventions
- Device: Transcranial direct current stimulation (tDCS)Drug: anti-CGRP-mAbs
- Registration Number
- NCT06079801
- Lead Sponsor
- Clínica de Intervención en Neurociencias
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 36
- 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.
- 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.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Real tDCS Transcranial direct current stimulation (tDCS) 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 anti-CGRP anti-CGRP-mAbs Patients will undergo anti-CGRP treatment Sham tDCS Transcranial direct current stimulation (tDCS) 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
- Primary Outcome Measures
Name Time Method Headache Impact Test (HIT-6) score baseline, 2 weeks after the end of the treatment, 6 months 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.
Migraine attacks monthly frequency baseline, 2 weeks after the end of the treatment, 6 months Patients will report migraine monthly frequency for the 3 different time-points
Pain killer drugs monthly taken baseline, 2 weeks after the end of the treatment, 6 months Patients will report pain-killer drugs taken during a month for the 3 different time-points
- Secondary Outcome Measures
Name Time Method The Pittsburgh Sleep Quality Index (PSQI) baseline, 2 weeks after the end of the treatment, 6 months 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) baseline, 2 weeks after the end of the treatment, 6 months 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.
Trial Locations
- Locations (1)
Clinica de Intervencion en Neurociencias
🇪🇸Talavera De La Reina, Toledo, Spain