Obesity
Conditions
Interventions
A sample of 60 adolescents will be formed, which will be divided into two groups with the same number of members.
Experimental Group: 30 adolescents with overweight and obesity will receive nutritiona
Behavioural
Other
E02.760.169.063.500.387
F04.754.137
Sponsors
Universidade do Sul de Santa Catarina
Universidade do Sul de Santa Catarina
Eligibility
Age
12 Years to 17 Years
Inclusion criteria
Inclusion criteria: Adolescents of both sexes; with ages between 12 years and 18 years incomplete; who have the capacity to understand the questionnaires; to sign the Terms of Free and Informed Consent; that they deliver the Term of Free and Informed Consent signed by the legal representatives; who are in pubertal stage three, four or five; which has a BMI greater than one standard deviation above the median BMI according to the WHO growth reference table for each age; who has not performed regular physical exercises in the last 3 months that will precede the start of the research; who have the physical conditions to perform regular physical exercises; who is willing to attend interventions; who has never had drug treatment for weight loss; that does not make chronic use of alcohol.
Exclusion criteria
Exclusion criteria: Adolescents with a history of alcohol or drug abuse; who have diseases that limit exercise or put their physical integrity at risk, such as cardiovascular diseases, osteoarticular diseases, type I diabetes, renal failure, endocrine diseases and metabolic complications such as hyperinsulinemia and hypercholesterolemia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in body composition and anthropometric parameters (reduction of body fat percentage and circumference measurements), verified by anthropometry and electrical bioimpedance, based on the statistical difference (p <0.05) between the assessments made before and after intervention period. | — |
Secondary
| Measure | Time frame |
|---|---|
| Reduction of the lipid profile (triglycerides, total cholesterol and fractions), verified by venipuncture and analyzed by the colorimetric method, based on the statistical difference (p <0.05) between the evaluations made before and after the intervention period. | — |
Countries
Brazil
Contacts
Public ContactFabricio Souza
Universidade do Sul de Santa Catarina
Outcome results
None listed