Bariatric Surgery
Conditions
Interventions
Randomized, controlled clinical trial with three parallel arms: face-to-face intervention group, virtual intervention group and waiting list control group. The study aims to evaluate the efficacy and
F04.754.137.350
Sponsors
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Eligibility
Age
30 Years to 65 Years
Inclusion criteria
Inclusion criteria: Aged between 30 and 65 years; both sexes; bariatric surgery performed in 2018 at the Hospital das Clínicas, Faculty of Medicine, University of São Paulo (USP); availability to participate in the sessions and assessments; internet access (for the virtual group)
Exclusion criteria
Exclusion criteria: Age under 30 or over 65 years; pregnancy; physical or cognitive impairment preventing participation in the sessions; refusal to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome: It is expected a reduction in depression and binge eating scale scores in the virtual and face-to-face intervention groups ;Outcome found: All three groups showed reductions in depressive symptoms, anxiety, and binge eating after the intervention, with these improvements maintained at follow-up. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome: It is expected reduction in body mass among participants in the virtual and in-person intervention groups;Outcome found: A marginal reduction in body mass and abdominal circumference was also noted across groups | — |
Countries
Brazil
Contacts
Public ContactVanessa Ponstinnicoff de Almeida
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Outcome results
None listed