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NCT07062315Enrolling by invitation

Impact of Chronotype-Based Time-Restricted Eating on Visceral Fat and Metabolic Health in Physically Inactive Adults With Central Obesity

Source: ClinicalTrials.gov · Last updated 31 Aug 2026

Brief summary (registry, in English)

Time-restricted eating (TRE) has gained attention as a promising dietary strategy for enhancing body composition and metabolic health. This innovative eating pattern involves confining daily food intake to a specific window, typically spanning 6-10 hours. Given the lack of consensus on the optimal TRE strategy, this research explores whether tailoring eating windows to individual chronotypes enhances TRE outcomes. This randomized controlled trial aims to evaluate the effects of chronotype-matched versus chronotype-unmatched TRE protocols, compared to a control group, over a 12-week period on visceral fat mass and other metabolic health outcomes in physically inactive adults with central obesity. Additionally, the study seeks to determine whether chronotype-matched TRE offers greater benefits in terms of visceral fat reduction and metabolic improvements compared to chronotype-unmatched TRE. Assessments will be conducted at baseline, and after the 12-week intervention.

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
90 (estimated)
First submitted
24 Jun 2025
Start date
31 Jul 2025
Primary completion date
Oct 2026
Lead sponsor
Chinese University of Hong Kong
Diseases
Obesity
NCT number
NCT07062315

What you commit to

  • Study type: Interventional
  • Planned participants: 90
  • From 31 Jul 2025 to the primary completion date, Oct 2026
  • 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

  • Individuals currently or chronically receiving pharmacological treatment for hypertension, diabetes, weight loss, or other metabolic conditions;

Other illness

  • Individuals with eating disorders;

Other

  • Night shift workers;
  • Female participants who are breast-feeding, pregnant, or attempting to become pregnant;
  • Individuals currently participating in other weight-management programs or following other prescribed diet programs.

Who the study is looking for

  • Chinese adults, male or female, aged between 18-65 years old;
  • BMI of 23 kg/m² or higher, with a waist circumference exceeding 80 cm for females and 90 cm for males;
  • Weight stability for at least three months prior to the start of the study;
  • Physically inactive, indicated by not meeting established WHO guidelines on physical activity and sedentary behavior (i.e., at least 150-300 minutes of moderate-intensity or at least 75-150 minutes of vigorous-intensity aerobic exercise; or an equivalent combination of moderate and vigorous-intensity activity throughout the week;
  • Baseline eating duration exceeding 10 hours per day;
  • Identified as either early or late chronotypes (Morningness-Eveningness Questionnaire)

Age in the registry: 18 years to 65 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
Department of Sports Science and Physical Education, The Chinese University of Hong Kong
Coordinator of this site? Confirm its status
Hong KongChinaUnknown status

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