Obesity
Conditions
Interventions
An intervention study will be performed with 30 obese children. During the study, the 30 patients selected will have the necessary samples to perform all the clinical analyzes collected on the day of
and group B, who will initially receive chia capsules, will receive placebo at this time. At the end of this new interval of 75 days, in the D165 will be collected the new samples necessary to carry o
Dietary supplement
SP6.051.227
Sponsors
Faculdade de Medicina do ABC - FMABC
Faculdade de Medicina do ABC - FMABC
Eligibility
Age
5 Years to 10 Years
Inclusion criteria
Inclusion criteria: Children in the pre-pubertal age of 5 to 10 years, with a 95th percentile greater.
Exclusion criteria
Exclusion criteria: Serological comorbidities (HIV, Hepatitis B, Hepatitis C), neoplasms, inflammatory diseases and patients who have been hospitalized in the last six months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Outcome 1: To verify the levels of vitamin E when associated to the use of chia seed and its effect on oxidative stress through biochemical and molecular biology exams before and after treatment with the seed. Only a greater variation of the serum vitamin value was observed in the group receiving chia supplementation than in the placebo group p 0.303.;Outcome 2: To verify if there was improvement in the inflammatory profile with the use of the chia seed, using methods of biochemical tests and molecular biology. It was possible to verify a statistically significant correlation between the delta of the markers and the presence of fiber in two inflammatory parameters: the TNF, with a p of 0.027 and the nf-Kappa ?, with a p of 0,059. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected. | — |
Countries
Brazil
Contacts
Public ContactCamila da Silva
Faculdade de Medicina do ABC - FMABC
Outcome results
None listed