MedPath

Mindful Eating for Eating Behavior Individuals Overweight and Obesity

Not Applicable
Completed
Conditions
Behavior, Eating
Overweight and Obesity
Feeding Patterns
Registration Number
NCT05845411
Lead Sponsor
Federal University of Health Science of Porto Alegre
Brief Summary

This clinical trial aims to compare the effect of a nutritional intervention based on Mindful Eating, with standard dietary treatment, in changing the eating behavior of overweight individuals.

Detailed Description

This clinical trial aims to compare the effect of a nutritional intervention based on Mindful Eating, with standard dietary treatment, in changing the eating behavior of overweight individuals. The main questions to answer are:

* What is the effect of the intervention on the domains of eating behavior (emotional eating, cognitive restriction, and lack of food control - assessed by the Three-Factor Eating Questionnaire R21)? ,

* Assess the effect of the intervention on weight and BMI.

* Evaluate the relationship between eating behavior domains before and after the intervention.

Participants in the intervention group will participate in eight sessions of a virtual therapeutic group, with up to fifteen individuals, every fifteen days, in which the theme of Mindful Eating and eating behavior will be worked. Participants will be encouraged to undertake the following:

* self-knowledge exercises between one session and another.

* mindfulness meditations daily. No dietary plan will be provided.

The researchers will compare the results with a control group, which will receive eight individual, fortnightly, and virtual consultations of conventional dietary treatment, which will provide:

* dietary plan for weight reduction, according to current guidelines.

* six food and nutrition education sessions based on the Food Guide for the Brazilian Population.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • body mass index greater than or equal to 25 kg/m²,
  • internet access,
  • availability to participate in 8 virtual meetings.
Exclusion Criteria
  • volunteers using pharmacotherapy for obesity,
  • pregnancy,
  • lactation,
  • cognitive conditions, self-reported neurological or psychiatric disorders that prevent participation in the study,
  • decompensated thyroid disorders, and
  • who have undergone bariatric surgery.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change in eating behaviorFour months

Sub-divided into domains: uncontrolled eating (UE), cognitive restriction (CR), and emotional eating (EE).

Secondary Outcome Measures
NameTimeMethod
Body weightFour months

in kilos

Body Mass Index - BMIFour months

in kg/m²

Trial Locations

Locations (1)

Federal University of Health Sciences of Porto Alegre

🇧🇷

Porto Alegre, Rio Grande Do Sul, Brazil

Federal University of Health Sciences of Porto Alegre
🇧🇷Porto Alegre, Rio Grande Do Sul, Brazil
© Copyright 2025. All Rights Reserved by MedPath