Risk factors present in metabolic syndrome may be improved through a change in lifestyle. Metabolic syndrome X, life style.
Conditions
Interventions
A randomized, blinded, controlled. 120 participants will be randomly divided into three groups: standard Intervention (IP) or control group: the volunteers of this group have two queries, one at the t
behavioural
other
F01.829.458
I02.233.332
G11.427.590.530.698.277
SP6.026
Sponsors
Pontifícia Universidade Católica do Rio Grande do Sul
Pontifícia Universidade Católica do Rio Grande do Sul
Eligibility
Age
30 Years to 59 Years
Inclusion criteria
Inclusion criteria: Men and women between 30 and 59 years of age with an abdominal circumference higher than 88 cm for women and higher than 102 cm for men and two (02) or more of the following findings:Blood pressure: systolic equal or higher than 130 mmHg and diastolic equal or higher than 85 mmHg; fasting glucose: equal or higher than 100 mg/dl; triglycerides:equal or higher than 150 mg/dl; HDL cholesterol less than 40 mg/dl for men and less than50 mg/dl for women.
Exclusion criteria
Exclusion criteria: Absolute contraindication to physical activity for musculoskeletal problems, neurological, vascular events (intermittent claudication), lung and heart; Presence of a diagnosis of severe psychiatric disorders and / or presence of significant cognitive impairment assessed by the team through the Mini-Mental State Examination; Difficult to contact and inability to return and follow-up, not available to participate in the program.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of at least 5% in waist circumference at the end of the intervention,in the three intervention groups, measured by abdominal perimeter. | — |
Secondary
| Measure | Time frame |
|---|---|
| Reduction of at least 20% of plasma triglycerides at the end of the intervention, in the three intervention groups, as assessed by laboratory tests.;Reduction of at least 20% in plasma glucose levels at the end of the intervention,in the three intervention groups, as assessed by laboratory tests.;Reduction of at least 7% in systolic blood pressure at the end of the intervention,in the three intervention groups,as assessed in the sitting position after 5 minutes of rest.;Increase of at least 5% of the plasma HDL cholesterol at the end of the intervention,in the three intervention groups, as measured by the laboratory test. | — |
Countries
Brazil
Contacts
Public ContactAna Pandolfo Feoli
PUCRS
Outcome results
None listed