Effect of a lifestyle change program for the treatment of Obesity with online and in person support

Not Applicable

• Conditions: Obesity; SP6.990

• Registration Number: RBR-10wpdd9c
• Lead Sponsor: Hospital das Clínicas da Faculdade de Medicina de São Paulo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2024-01-10
• Last Update Posted: 23 January 2024
• Study Completion: 2024-03-01

Recruitment & Eligibility

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

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

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

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.