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Brazilian headache registry: methods and preliminary data of the pilot study
Vanise Grassi1,2,3, Mauro Eduardo Jurno4,5, Alan Christmann Fröhlich6
1Hospital Moinhos de Vento, Porto Alegre RS, Brazil.
Arquivos De Neuro-Psiquiatria
|August 21, 2023
Summary
The Brazilian Headache Registry pilot study demonstrated feasibility for collecting data on primary and secondary headaches. This initiative aims to improve understanding of headache phenotypes and healthcare resource utilization in Brazil.
Area of Science:
- Neurology
- Public Health
- Epidemiology
Background:
- Headache evaluation and treatment pose a global public health challenge.
- The Brazilian Headache Society initiated the Brazilian Headache Registry to address the epidemiological impact of headaches.
- A protocol was developed for this multicenter longitudinal observational study.
Purpose of the Study:
- To describe the methods and preliminary data from the pilot phase of the Brazilian Headache Registry.
- To assess the feasibility of the developed research protocol in tertiary headache care centers.
- To lay the groundwork for a comprehensive database for characterizing headache patients and healthcare resource use.
Main Methods:
- A multicenter longitudinal observational study was conducted from September 2020 to August 2021.
- Prospective data were collected from 66 eligible patients (≥18 years) across three specialist headache centers in Brazil.
- Inclusion criteria involved seeking care for headache in tertiary centers and willingness to participate.
Main Results:
- The pilot study included 66 patients, predominantly female (90%) with a mean age of 38.2 years.
- Primary headaches represented 85.3% of diagnoses, while medication overuse headache was the most common secondary headache (7.1%).
- Data were collected from patients in Rio Grande do Sul (65%) and Minas Gerais (35%) states.
Conclusions:
- The pilot study confirmed the feasibility of the research protocol for tertiary care settings.
- The Brazilian Headache Registry will provide longitudinal data to better characterize headache phenotypes.
- The registry aims to detail health resource use and identify predictors of clinical outcomes for headache patients.

