Responses of physical training on the metabolism and body fat of adolescents.

Not Applicable

• Conditions: Overweight; Obesity; C23.888.144.699; C18.654.726.500

• Registration Number: RBR-35jq4c
• Lead Sponsor: Departamento de Educação Física (DEF), da Universidade Federal do Paraná (UFPR)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-05-21
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Conditions to participate in all evaluations
and / or intervention; presentation of the informed consent form (TCLE) and free and informed consent form (TALE) signed; individuals of both sexes between, 13 and 17 years of age; pubertal staging Tanner IV; individuals classified as eutrophic (BMI not presenting clinical conditions such as: established diagnosis of type 1 or type 2 diabetes, familial dyslipidemia and / or treatment with statins, Untreated or uncontrolled hypothyroidism / hyperthyroidism; obesity induced by other endocrine disorders, delayed significant puberty of any etiology requiring investigation and / or treatment,
patients with a diagnosis or suspicion of growth hormone deficiency, severe asthma requiring frequent hospitalizations or use of systemic corticosteroids for more than 10 days, a history of current treatment or treatment with medications that may cause significant weight gain within three months prior to the screening visit, including corticosteroids (bariatric surgery less than 7-10 days), tricyclic antidepressants, antipsychotics and mood stabilizers, previous surgical treatment for obesity (Bariatric Surgery), known or suspected alcohol, drug or narcotic abuse, recent infections or the presence of acute inflammatory disease or chronic, genetic syndromes that lead to obesity.

Exclusion Criteria

To present some intercurrence that would make continuity of the intervention and / or evaluations impossible; participation in other activities that interfered in the results of the research such as (sports practice or systematic exercise, diets, other treatments); less than 70%.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Expected primary outcome 1<br>The outcome will be considered effective if observed between the group and time (any measured moment compared to the pre-intervention moment) with p-value less than 0.05 (variation of 5%), with a decrease in serum C-reactive protein in mg/dl, analyzed by the Enzyme-Linked Immunosorbent Assay (ELISA) technique.;Expected primary outcome 2<br>The outcome will be considered effective if observed between the group and time (any time measured compared to the pre-intervention time) with p value less than 0.05 (variation of 5%), with improvement of the serum metabolic profile (metabolits in mg/dl) evaluated by nuclear magnetic resonance.