Obesity
Conditions
Interventions
This is a clinical study with randomization of two groups: intervention and control. Randomization will be carried out alternately, according to the week of care, in order to avoid sharing information
G07.203.650.240
F04.754.137.350
Sponsors
Hospital das Clínicas da Faculdade de Medicina de São Paulo
Hospital das Clínicas da Faculdade de Medicina de São Paulo
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Minimum age of 18 years; body mass index (BMI) equal to or greater than 30; have a smartphone with internet access
Exclusion criteria
Exclusion criteria: patients not adhering to the project proposal; undergoing bariatric surgeries; pregnant women; breastfeeding women; illiterate individuals; people with endocrine diseases; genetic syndromes that cause obesity; cognitive deficit; uncontrolled psychiatric illness
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Weight loss of 5% of the patient's total weight is expected, using the bioimpedance method in the first and last week of the study. | — |
Secondary
| Measure | Time frame |
|---|---|
| An improvement in the lipid profile is expected, measured through laboratory tests carried out in the first and last week of the study.;An improvement in depressive, anxiety and stress symptoms, measured using the depression, anxiety and stress scale (DASS-21) is expected in the first and last week of the study.;An improvement in the nutritional quality of the diet is expected, measured through food intake records (RCA) collected in the first and last week of the study. | — |
Countries
Brazil
Contacts
Public ContactGraziele Coelho
Hospital das Clínicas da Faculdade de Medicina de São Paulo
Outcome results
None listed