Multidisciplinary Program of Treatment of Obesity: Evaluation of Cardiometabolic Risk Factors

Not Applicable

Recruiting

• Conditions: Overweight; Obesity; Abdominal Obesity; Morbid Obesity; C23.888.144.699; C18.654.726.500; C18.654.726.500.697; C18.654.726.500.700

• Registration Number: RBR-2yzs76
• Lead Sponsor: niversidade Estadual de Maringá

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-07-06
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

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

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;

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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<br>readiness for change, quality of life, physical activity level and eating habits.