Fibromyalgia
Conditions
Interventions
This is a randomized, crossover, sham-controlled clinical trial that will be conducted with 14 women diagnosed with fibromyalgia, following the American College of Rheumatology (ACR) criteria. The stu
consequently, the participant will not rec
E02.331.800
Sponsors
Universidade Federal de Santa Catarina - UFSC
Universidade Federal de Santa Catarina - UFSC
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Female individuals; age between 18 and 65 years old; patients with fibromyalgia; walk independently; understand brazilian portuguese
Exclusion criteria
Exclusion criteria: IIndividuals with red flags like fracture or cancer; suspected or confirmed pregnancy; unstable heart conditions; absence of ear
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find a reduction in the intensity and distribution of perceived pain, by at least two points in the intervention group | — |
Secondary
| Measure | Time frame |
|---|---|
| Assess cognitive function at the beginning and end of the study;Assess heart rate variability at the beginning and end of the study;Assess the serum concentration of Brain-Derived Neurotrophic Factor (BDNF) at the beginning and end of the study | — |
Countries
Brazil
Contacts
Public ContactMarcos Neves
Universidade Federal de Santa Catarina
Outcome results
None listed