Overweight
Conditions
Interventions
The intervention groups (GII and GISUS) and control (GC) will be composed of 20 participants in the city of Maringá and 15 of Paranavaí, totaling 35 subjects in each group.
The control group (GC) per
and in the second hour, apply the exercise sessions. Based on cognitive behavioral therapy, the focus of the program will contribute to the process of changing food behaviours and physical activity pr
Behavioural
Other
SP6.026
G11.427.410.698.277
Sponsors
Universidade Estadual de Maringá
Universidade Estadual do Paraná
Hospital Universitário de Maringá
Eligibility
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Age between 18 and 50 years; Being overweight or obese, from cutting index points Body mass index greater than or equal 25; Waist circumference greater than or equal 88 cm for women and greater than or equal 102 cm for men; Be resident in Maringa or Maringá metropolitan area; Present willingness to participate in the evaluations of the risk cardiometabólico; Agree and sign the informed consent approved by the local Ethics Committee.
Exclusion criteria
Exclusion criteria: Recent abdominal surgery or Bariatric Surgery; Pulmonary disease with oxygen dependence; Hospitalization for treatment of cardiovascular diseases in the last 6 months; Aortic stenosis; Being pregnant or have less than 3 months post partum; Use of medicines for weight loss; Using glicocorticoides;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome 1 provided for this study will be anthropometric parameters (body weight, BMI and waist circumference).;The primary outcome 2 planned for the present study will be parameters of body composition (fat mass, fat%, fat free mass, fat free mass%). | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome 1 provided for this study will be the metabolic changes (blood glucose, glycated hemoglobin, insulinemia and lipid profile).;The secondary outcome 2 planned for the present study is physical fitness (flexibility, strength/muscular endurance and cardio-respiratory fitness).;The secondary outcome 3 provided for this study will be the inflammatory parameter measured by C-reactive protein ultra sensible.;The secondary outcome 4 referred to the present study are the cardiovascular parameters (heart rate variability, systolic and diastolic blood pressure, carotid intimal middle layer and cardiac geometry).;The secondary outcome 5 scheduled for the present study is the change in lifestyle measured by assessment instruments readiness for change, quality of life, physical activity level and eating habits. | — |
Countries
Brazil
Contacts
Public ContactNelson Prof. Nelson - NEMO/HUM/UEM
Hospital Universitário de Maringá
Outcome results
None listed