TEFALEffects of Weight Loss on Dietary Thermogenesis in Obese Adolescents
This study aims to investigate how weight loss affects the energy your body uses to digest food, known as dietary thermogenesis, in adolescents who are obese.
Anthropometric measurements
+ Body composition assessment
+ Leeds Foods Preference Questionnaire
Body Weight+5
+ Nutrition Disorders
+ Nutritional and Metabolic Diseases
Other Study
Summary
Study start date: February 28, 2026
Actual date on which the first participant was enrolled.This study focuses on understanding the role of dietary thermogenesis, which is the energy we use to digest food, in obese adolescents. It's important to note that while resting metabolism and energy expenditure from physical activity are major contributors to total energy expenditure, dietary thermogenesis can also account for about 10% of our daily energy use. Some studies suggest that the thermic effect of food (TEF), or the increase in energy expenditure after eating, may be lower in individuals with obesity. This could potentially play a role in the development or maintenance of obesity. However, there's a lack of consensus on this topic, especially when it comes to children and adolescents. This study aims to fill this gap and explore whether TEF is indeed reduced in obese adolescents, which could help optimize their daily energy balance. The study will evaluate the effects of weight loss on dietary thermogenesis in obese adolescents. Participants will undergo a weight loss intervention, and their postprandial energy expenditure (PEE), or the energy used to digest food after a meal, will be measured. This will be compared with the PEE of adolescents with normal weight. The study also aims to understand how weight status, body composition, and the caloric composition of a meal might influence TEF in this population. The primary outcome of the study is to measure changes in PEE after weight loss.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.30 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Other 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 11 to 17 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.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Laboratoire AME2P, Université Clermont Auvergne
Aubière, FranceOpen Laboratoire AME2P, Université Clermont Auvergne in Google Maps