Obesity, metabolic syndrome
Conditions
Interventions
In total, 75 patients should be randomized to one of the three experimental groups, detailed below: 1) Continuous aerobic training (n = 25)
2) High intensity interval training (n = 25)
and 3) Control (n = 25). Each group will consist of 25 volunteers. It is emphasized that all volunteers should carry out a personalized diet to reduce body weight.
After the preliminary evaluation of
Other
E02.642.249.285
Sponsors
Universidade Federal do Rio Grande do Norte - UFRN
Universidade Federal do Rio Grande do Norte - UFRN
Eligibility
Age
20 Years to 45 Years
Inclusion criteria
Inclusion criteria: Volunteers should not be engaged in exercise programs; body mass index between 30 and 39,9; body mass stability in the last six months.
Exclusion criteria
Exclusion criteria: Current smokers; body mass index greater than 40; have a clinical diagnosis of chronic non-communicable diseases; pregnant; postpartum; breastfeeding.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Insulin resistance: will be assessed from the HOMA index, which takes into account biochemical measurements of glucose and insulin. A 10% reduction in the value of HOMA will be considered satisfactory. | — |
Secondary
| Measure | Time frame |
|---|---|
| Lipid profile: will be evaluated through the biochemical measurements of total cholesterol and its fractions, and triglycerides. To be considered as reached, individuals are expected to reach normal values in these parameters, ie total cholesterol 40 mg / dL, LDL cholesterol <160 mg / dL and triglycerides <150 mg / dL.;Body composition: assessed by DEXA imaging. A reduction of at least 10% in your total fat mass is expected. | — |
Countries
Brazil
Contacts
Public ContactAna Paula Fayh
Universidade Federal do Rio Grande do Norte - UFRN
Outcome results
None listed