Professional Burnout
Conditions
Interventions
This is a controlled prospective clinical trial with two parallel groups, open label, with no masking, no placebo and no washout period, with a total duration of four months. A total of 71 healthcare
Sponsors
Hospital Israelita Albert Einstein
Hospital Israelita Albert Einstein
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Healthcare professionals; both sexes; age between 18 and 65 years; active professional link with the institution; day, evening, or night work shift; agreement to participate and provision of written informed consent; clinical ability to participate in a lifestyle change program including nutritional guidance and encouragement of physical activity.
Exclusion criteria
Exclusion criteria: Uncontrolled chronic diseases; clinical or physical conditions that prevent safe participation in a lifestyle change program including nutritional guidance and encouragement of physical activity; use of medications that significantly interfere with body weight or body composition; pregnancy; breastfeeding; concurrent participation in another intervention study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in lean mass, body fat percentage, and total body water measured by segmental bioelectrical impedance analysis (InBody S10) from baseline to week 12. | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in self-reported burnout symptoms assessed by a 26-item structured questionnaire from baseline to week 12.;Change in lifestyle behaviors (physical activity, hydration, diet) measured by structured questionnaire from baseline to week 12. | — |
Countries
BR
Contacts
Public ContactGabriel Yacoub
Hospital Israelita Albert Einstein
Outcome results
None listed