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Effectiveness of a Mindful Eating for Health Program among Hospital Staff

Effectiveness of a Mindful Eating for Health Program among Hospital Staff: a pragmatic mixed-methods randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-23h6k87
Enrollment
Unknown
Registered
2024-03-18
Start date
2023-10-20
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Feeding behavior

Interventions

Mindfulness-Based Interventions have shown promising results for comprehensive health care and eating behavior. Although extensively studied in the United States and Europe, there have been relatively

Sponsors

Universidade Federal de São Paulo
Lead Sponsor
Universidade Federal de São Paulo
Collaborator
Instituto de Gastroenterologia de São Paulo Centro Médico e Cirúrgico
Collaborator

Eligibility

Age
20 Years to 59 Years

Inclusion criteria

Inclusion criteria: Adults; aged 20 to 59; both genders; body mass index equal to or greater than 18.5 kg/m² and less than 40 kg/m²

Exclusion criteria

Exclusion criteria: Individuals undergoing pharmacological treatment for obesity; pregnancy; individuals with untreated hypothyroidism or hyperthyroidism (TSH 5.5 mlU/mL) or treated less than 6 months ago; individuals in an acute phase of depression (less than 6 months in depression), those with schizophrenia or psychotic disorders, or those using medication that causes cognitive, attention, and concentration impairments (such as potent anxiolytics); practitioners of mindfulness, meditation, yoga, or similar practices within the last 6 months (with formal practice at least once a week); individuals who have undergone any type of bariatric surgery; extreme obesity (BMI equal to or greater than 40 kg/m²); participation in other clinical intervention studies; chronic kidney disease, heart failure, and other clinical conditions that may interfere with fluid balance; individuals who received nutritional guidance in the last 6 months; individuals being diagnosed with anorexia nervosa

Design outcomes

Primary

MeasureTime frame
It is expected the improvement of eating behavior (cognitive restraint, emotional eating, and uncontrolled eating). TIME FRAME: Baseline (pre-intervention), week 8 (post-intervention), and 3-, 6- and up to 12-month follow-up.

Secondary

MeasureTime frame
It is expected an increase in the levels of mindfulness, a reduction in the levels of depression, anxiety, an improvement in the levels of self-compassion, an improvement in the levels of self-care, to lower the levels of perceived stress, and an improvement in nutritional status (among those who are overweight). TIME FRAME: Baseline (pre-intervention), week 8 (post-intervention), and 3-, 6- and up to 12-month follow-up.

Countries

Brazil

Contacts

Public ContactFernanda Magalhães

Universidade Federal de São Paulo

fgmagalhaes88@gmail.com+55(11)21490155

Outcome results

None listed

Source: REBEC (via WHO ICTRP)