Morbit, Obesity
Conditions
Interventions
This is a clinical study, controlled, prospective, milticentric with 250 pacients. Experimental group: 125 individuals with severe obesity will receive nutritional guidance (mindful eating) weekly, p
healthy eating
physical exercise to promote health and weight loss
7 bariatric surgery. The interventions will be offered remotely for a period of 12 weeks.
F04.754.137.350
Sponsors
Escola Superior de Educação Física da Universidade de Pernambuco
Universidade de Pernambuco
Eligibility
Age
18 Years to 59 Years
Inclusion criteria
Inclusion criteria: Volunteers eligible for bariatric surgery; both sexes; non-smokers; between 18 and 59 years old; body mass index greater than or equal to 35 kg/m² in the population with comorbidities; and body mass index greater than or equal to 40 kg/m² in the population without comorbidities
Exclusion criteria
Exclusion criteria: Super obese volunteers (body mass index greater than 50kg/m²); diagnosed with cardiac pathologies; who cannot exercise due to musculoskeletal health conditions; does not have internet access to follow interventions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find, through analyses of pro-oxidant and antioxidant markers (NADPH, NOX1, NOX2, NOX3; MDA, DPPH, SOD1, SOD3, Catalase, Glutathione reductases) significant changes in the profile of oxidative stress in the population with severe obesity at the beginning and at the end of the study ;It is expected to find, through analyses of blood pressure, mediated dilator function, heart rate variability, a reduction in cardiovascular risk in the population with severe obesity at the beginning and end of the study | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find significant changes in the index of anxiety and depression symptoms at the beginning and end of the study; - It is expected to obtain significant changes in the inflammatory and anti-inflammatory profile in the population with severe obesity at the beginning of the study and at the end of the study ;It is expected to find a weight loss equal to or greater than 10% of the initial weight, as well as significant reductions in body composition measurements at the beginning of the study and at the end of the study;It is expected to find significant changes in the index of binge eating symptoms at the beginning and end of the study | — |
Countries
Brazil
Contacts
Public ContactAline Brito
Universidade de Pernambuco
Outcome results
None listed