Migraine Disorders. Migraine without Aura. Migraine with Aura
Conditions
Interventions
This is a non-blind, single-group feasibility study with 12 women diagnosed with migraine. 8 Transcranial Magnetic Stimulation (TMS) sessions will be carried out in the left dorsolateral prefrontal co
E02.621.820
F02.463.551
Sponsors
Centro de Ciências da Saúde da Universidade Federal do Espírito Santo
Centro de Ciências da Saúde da Universidade Federal do Espírito Santo
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Women (cis or trans). Aged between 18 and 65 years old. Present a diagnosis of Migraine according to the criteria of The International Classification of Headache Disorders (ICHD-3) 2018, for more than 3 months: at least five attacks meeting criteria from B to D; headache attacks lasting 4-72 hours (without treatment or with ineffective treatment); the headache has at least two of the following characteristics: unilateral location, pulsatile character, moderate or severe pain intensity, exacerbated by or causing the individual to avoid routine physical activities (for example: walking or climbing stairs); during headache, at least one of the following: nausea and/or vomiting, and photophobia and phonophobia, not better explained by another ICHD-3 diagnosis
Exclusion criteria
Exclusion criteria: Participants who are at a peak of cardiovascular disease or have severe cardiopulmonary disease. With sequelae of neurological diseases. Use walking aids. With visual and hearing impairments. With amputations of lower and upper limbs. With rheumatic diseases in the acute phase. Cancer. Epilepsy. Fractures of the skull, neck or rib cage. Severe osteoporosis. People with a pacemaker or implantable cardioverter defibrillator, epilepsy or who underwent surgery less than 1 year ago. Pregnant or breastfeeding women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The feasibility of the study for the future development of a clinical trial. | — |
Secondary
| Measure | Time frame |
|---|---|
| The recruitment rate, patient adherence rate to the treatment protocol, the acceptability of the intervention by the participants and the safety of the intervention protocol. | — |
Countries
Brazil
Contacts
Public ContactSynthia Marcolano
Universidade Federal do Espírito Santo
Outcome results
None listed