Actively Recruiting
The Effect of Time-Restricted Feeding on Body Composition and Some Metabolic Parameters in Obese Adolescents
Led by Sümeyra Başar · Updated on 2025-02-25
60
Participants Needed
1
Research Sites
43 weeks
Total Duration
On this page
Sponsors
S
Sümeyra Başar
Lead Sponsor
H
Health Institutes of Turkey
Collaborating Sponsor
AI-Summary
What this Trial Is About
Obesity is now recognized as a serious public health problem. It is known that obesity seen in adolescence is largely carried over to adulthood. Therefore, its treatment is important both in terms of protecting current health and preventing diseases in adulthood. Reducing energy intake plays an important role in the treatment of obesity. However, long-term adherence and effectiveness to energy restriction appear to be limited. Therefore, the need for interventions that are "effective in body weight loss" and "accessible, simple and lifestyle modification to increase dietary compliance" is clear. Time-restricted feeding is a specialized intermittent fasting protocol that includes consistent fasting and eating periods over a 24-hour cycle by supporting circadian rhythms. Especially in the adult population, positive effects of time-restricted feeding such as weight loss and blood glucose regulation are observed. However, there are limited data on this subject for adolescents. Today, the Mediterranean diet, which is one of the nutrition models that supports health, is a beneficial nutritional model that reduces body weight and obesity-related comorbidities by limiting total energy intake. However, no study has been found in the literature in which the effectiveness of time-restricted nutrition, which is a new and promising approach, and the Mediterranean diet, which is a sustainable diet model, are evaluated together. Therefore, in this study, it was aimed to evaluate the effects of planned time-restricted nutrition compatible with circadian rhythm and energy-restricted feeding planned according to the Mediterranean diet model on body composition and various metabolic parameters in obese adolescents. 60 obese adolescents aged 12-18 years will be included in this randomized controlled and parallel design study. Participants will be randomized to one of two treatment groups for a 12-week intervention. The time-restricted feeding group will form the intervention group of the study, and the energy-restricted feeding group will form the control group. Anthropometric measurements of the participants at the beginning and end of the study will be taken, and various biochemical parameters will be evaluated with the body composition and blood samples to be taken. As a result of the study, it is expected to determine the effectiveness of time-restricted feeding compared to energy-restricted feeding in terms of dietary compliance, body composition and biochemical changes.
CONDITIONS
Official Title
The Effect of Time-Restricted Feeding on Body Composition and Some Metabolic Parameters in Obese Adolescents
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adolescents aged 12-18 with puberty stage 5
- Obese adolescents with a metabolic disorder such as fatty liver, insulin resistance, prediabetes, or dyslipidemia (BMI ≥ 95th percentile for age)
- Stable body weight for 3 months before the study (weight change less than 4 kg)
- Own and can use a smartphone with Apple iOS or Android operating system
- Speak, read, and understand Turkish
You will not qualify if you...
- Presence of any endocrine disorder, metabolic, chronic or major psychiatric disease other than obesity, insulin resistance, dyslipidemia, prediabetes, or fatty liver
- Diagnosis of polycystic ovary syndrome (PCOS)
- Physical or mental disabilities
- Allergies, intolerances, or eating disorders
- Smoking or alcohol use
- Use of medications affecting study results, circadian rhythms, or metabolism (such as antidiabetics, steroids, beta blockers, adrenergic stimulating agents, laxatives)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Mustafa Eraslan and Fevzi Mercan Children's Hospital
Kayseri, Turkey (Türkiye), 38039
Actively Recruiting
Research Team
S
Sümeyra Başar
CONTACT
Z
Zeynep Caferoğlu Akın
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here