Hypertension
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Hypertensive men and women; with proven diagnosis; adults; older than 20 years; who have not been on a diet for 6 months.
Exclusion criteria
Exclusion criteria: Users with any neurocognitive condition or mental disorder (defined by their clinical history or clinical investigation); pregnant women; nursing mothers; users with liver failure; previous history of encephalopathy or anasarca; renal failure; with indication for dialysis; severe congestive heart failure; previous organ transplantation; gastroplasty; life expectancy of less than 6 months; wheelchair user and with difficulty receiving oral diet.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Detect a difference of 7 mmHg in systolic blood pressure, determined using an electronic sphygmomanometer, at each visit from the beginning to the end of the study (monthly visits). | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. A 5% reduction in blood glucose is expected, as measured by laboratory tests performed at the beginning and at the end of the study.;2. Reduction of approximately 3.5% in the Body Mass Index, measured before and after intervention.;3. Reduction in calorie intake, measured by collecting a recall and calculating it in a specific program, by approximately 10% of daily calories. | — |
Countries
Brazil
Contacts
Universidade do Estado da Bahia