metabolic syndrome
Conditions
Interventions
This is a randomized clinical trial that will be conducted with three groups: 67 participants will be allocated to the intervention group, which will have access to the content of the interactive virt
67 participants will be in the second intervention group, which will be monitored by a health team composed of a doctor, nurse, nutritionist, and psychologist
and 66 participants will be in the control group, which will receive official documents from Brazilian societies and the Ministry of Health in individual sessions of 2 hours per week and a weekly virt
Sponsors
Universidade do Estado da Bahia
Universidade do Estado da Bahia
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Age 18 or older; both genders; occupational stress; presence of burnout symptoms (in all three dimensions); metabolic syndrome; willingness to voluntarily participate in the program
Exclusion criteria
Exclusion criteria: Those who participated in another study/body-mind therapy intervention in the last month; pregnant women; those on leave from work; those who do not complete all stages of the intervention
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that 50% of participating professionals will show improvement in occupational stress and burnout | — |
Secondary
| Measure | Time frame |
|---|---|
| A 20% reduction in abdominal circumference, weight, and blood pressure is expected, along with an improvement in lipid and glycemic profiles | — |
Countries
Brazil
Contacts
Public ContactMagno das Mercês
Universidade do Estado da Bahia
Outcome results
None listed