Obesity
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adult volunteers; 18 to 59 years of age; of both sexes; diagnosed with obesity to any degree for body mass index (BMI)
Exclusion criteria
Exclusion criteria: Eutrophic, overweight and malnourished volunteers for BMI; who have contraindications to rEMT or have received rEMT in the last 12 months; who present any head injury, previously documented epilepsy, presence of psychiatric disorder (schizophrenia and bipolar disorder); who have metal implants in their heads; who use or have used anti-obesity drugs (sibutramine, topiramate, orlistat and liraglutide) in the last 3 months; who are addicted to illicit drugs in the last 5 years; who have Cushing's Syndrome; who are pregnant or breastfeeding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find a reduction in subjective levels of hunger and increased satiety in obese patients, verified by the Visual Analogue Scale (VAS), from a reduction in measurements of 60% comparing sham group and treatment | — |
Secondary
| Measure | Time frame |
|---|---|
| A reduction of 5% in anthropometric measurements is expected, as verified by physical evaluation, comparing sham group and treatment;A reduction in the level of binge eating is expected to be 5%, verified by the Binge Eating Scale, comparing the sham group and treatment;Modifications in laboratory tests of 5% are expected, verified by biochemical tests, comparing sham group and treatment | — |
Countries
Brazil
Contacts
Instituto de Neuromodulação e Reabilitação Avançada (INERVA)