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NCT07055620Completed

Effects of Different Dietary Models on Eating Behavior and Obesity Management in Overweight and Obese Individuals

Effects of Different Dietary Models on Eating Behavior and Obesity Management in Overweight and Obese Individuals: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 25 Nov 2025

Brief summary (registry, in English)

The aim of this study is to examine the effects of different diet models (Mediterranean diet, time-restricted feeding and standard diet application) applied to overweight and obese individuals on eating behavior and obesity management. Sub-objectives can be listed as; Effects of different diet models on body composition, Effects of different diet models on dietary intake, Effects of different diet models on biochemical parameters (such as blood sugar, insulin resistance, lipid profile). As a result, this study aims to contribute to the development of individualized nutrition counseling programs by determining effective diet strategies in obesity.

Status (registry)
Completed
Study type
Interventional
Enrollment
75 (actual)
First submitted
19 Jun 2025
Start date
18 Apr 2025
Primary completion date
18 Jun 2025
Lead sponsor
Selcuk University
Diseases
Obesity
NCT number
NCT07055620

What you commit to

  • Study type: Interventional
  • Participants enrolled: 75
  • From 18 Apr 2025 to the primary completion date, 18 Jun 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Those who regularly use medications that affect metabolism,
  • Those who use insulin and oral antidiabetic medications,

Other illness

  • Those who have any chronic disease and are on a diet,
  • Those who have allergies or intolerances to any food components of the Mediterranean diet (walnuts, hazelnuts, peanuts, almonds, etc.),
  • Those who have a psychiatric disease diagnosed by a physician.

Other

  • Pregnant and breastfeeding women,
  • Those who could not attend one or more interview sessions,
  • Women who have entered menopause,
  • Individuals who want to apply another diet model,
  • Individuals who have a pacemaker or defibrillator implanted due to the theoretical possibility of interference with device activity due to the current field caused by impedance measurements,
  • Those who use vitamin/mineral supplements,
  • In order to understand the effectiveness of the diet, individuals will be asked to maintain their physical activity levels. Therefore, individuals who want to increase their physical activity levels in addition to the applied diet will not be included in the study.

Who the study is looking for

  • Being between 20-49 years old
  • Having a BMI value between 25 kg/m2- 35 kg/m2
  • Not having conditions that impair reality assessment ability and cognitive functions, preventing interviews or filling out scales
  • Being literate
  • Having a blood test done by a primary care physician within the last seven days
  • Agreeing to participate in the study and signing the informed consent form

Age in the registry: 20 years to 49 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Eda Ocak Nutrition and Diet Consultancy
Coordinator of this site? Confirm its status
KonyaTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.