Cognitive Behavioral Therapy and Motivational Interviewing in Obesity
Cognitive Behavioral Therapy- Based and Motivational Interviewing-Supported Psychoeducation
Body Weight+5
+ Nutrition Disorders
+ Nutritional and Metabolic Diseases
Treatment Study
Summary
Study start date: October 15, 2024
Actual date on which the first participant was enrolled.This study is exploring how a special educational program that combines cognitive-behavioral therapy techniques with motivational interviewing can help people with obesity manage emotional eating and increase their ability to handle stress and bounce back from challenges. The goal is to see if this approach can reduce the tendency to eat in response to emotions and improve mental resilience. This research is important because emotional eating can often hinder weight loss efforts, and enhancing psychological resilience might help individuals maintain healthier habits and improve overall well-being. Participants in the study will be divided into two groups: one receiving the psychoeducation program and the other not receiving any intervention. The program will be delivered as a structured course over eight weeks to the experimental group. Researchers will evaluate all participants at the beginning, after the eight weeks, and again three months later to measure changes in emotional eating and psychological resilience using specific scales designed for these purposes. The control group will allow researchers to compare results and determine the effectiveness of the intervention. This study aims to provide evidence on the benefits of psychological strategies in managing obesity.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.102 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.10 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalGroup III
ExperimentalGroup IV
ExperimentalGroup 5
ExperimentalGroup 6
ExperimentalGroup 7
ExperimentalGroup 8
ExperimentalGroup 9
ExperimentalGroup 10
ExperimentalStudy Objectives
Primary Objectives