hypertension, hypercholesterolemia, overweight, obesity
Conditions
Interventions
A non-randomized, non-blind, controlled clinical trial, two-arm of effectiveness . Intervention group: 260 patients attended in the primary health care unit – they will be exposed to healthy eating an
Sponsors
Universidade Federal de São Paulo
Secretaria Municipal de Saúde de São Paulo
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Healthy volunteer; both gender; more than 18 years old; overweight; diabetes mellitus; systemic arterial hypertension; dyslipidemia;
Exclusion criteria
Exclusion criteria: Mental deficiency; confusion; pregnant; nursing mother
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected an increase in the mean difference in one portion of unprocessed food. ;It is expected reduction in the mean difference in one portion of ultraprocessed food.;It is expected increase in the mean difference in one point score of the Brazilian Food Guide. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find mean difference at least 5% of glycemia.;It is expected to find mean difference at least 5% of uric acid.;It is expected to find mean difference at least 5% of creatinine.;It is expected to find mean difference at least 5% of cholesterol levels. | — |
Countries
Brazil
Contacts
Public ContactLuciana Tomita
Universidade Federal de São Paulo
Outcome results
None listed