About this trial
We are conducting this research in individuals with migraines to find out if a daily magnet helmet application could alter migraine-related brain inflammation. Outcomes will be assessed through examining any changes in Translocator Protein (TSPO) binding on Positron Emission Tomography-Computed Tomography (PET-CT) imaging both before and after the magnet helmet intervention period. Additionally, patient-reported migraine symptoms will be measured using validated questionnaires administered during the four-week pre- and post- intervention monitoring periods.
Eligibility criteria
Qualifiers
Between 18 and 65 years of age.
The frequency of migraine attacks must be at least 4 migraine-days per month.
The duration of the disease must be of at least one year.
Willingness to adhere to daily intervention sessions and complete study procedures.
Disqualifiers
Greater than 20 headache days per month.
Major systemic illness (e.g., brain tumor, severe hypertension) or unstable medical and/or psychiatric condition (e.g., suicide risk, requiring immediate treatment) that could compromise protocol adherence.
Evidence of relevant co-morbidity, systemic or not, with potential to substantially interfere with the phenotype of the conditions studied in the present protocol (e.g., history of Type I or Type II diabetes mellitus unless well managed).
A history of neurological disease or injury, including a history of seizures or significant head trauma (i.e., extended loss of consciousness, neurological sequelae, or known structural brain lesion), which may confound the results of the study.
Trial design
Treatments tested in this trial
- Static magnetic helmet
Treatment groups
Sponsors and collaborators
Marco Loggia
Lead sponsor
Massachusetts General Hospital
Sponsor institution