Impact of Chronotype-Based Time-Restricted Eating on Visceral Fat and Metabolic Health in Physically Inactive Adults With Central Obesity
NCT ID: NCT07062315
Last Updated: 2025-07-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
NA
90 participants
INTERVENTIONAL
2025-07-31
2026-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect of Time-Restricted Feeding on Fat Loss and Cardiometabolic Risk Factors in Overweight Adults
NCT03459703
Effects of Early and Late Time-restricted Eating on Overweight Adults With Metabolic Syndrome
NCT06018415
Effects of Early and Delayed Time-restricted Eating in Adults With Overweight and Obesity
NCT04647149
Effect of Time-restricted Eating on Catecholamine-sensitivity of Adipose Tissue in Obese Adults
NCT04916730
Time Restricted Eating for Weight Management
NCT04692532
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Chronotype-matched TRE
Participants will eat ad libitum within an 8-hour eating window that match their chronotype.
Chronotype-matched time-restricted eating
A 12 weeks time-restricted eating intervention that match participants' chronotype
Chronotype-unmatched TRE
Participants will eat ad libitum within an 8-hour eating window that unmatch their chronotype.
Chronotype-unmatched time-restricted eating
A 12 weeks time-restricted eating intervention that not match participants' chronotype
Waitlist control
Participants in the waitlist control group will be instructed to maintain their previous eating or physical activity habits during the 12-week intervention. They will not receive any specific dietary advice or guidance. Weekly check-ins will be conducted to confirm continued participation and adherence. If they wish to participate, we will provide a suitable intervention after the duration of the study period.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Chronotype-matched time-restricted eating
A 12 weeks time-restricted eating intervention that match participants' chronotype
Chronotype-unmatched time-restricted eating
A 12 weeks time-restricted eating intervention that not match participants' chronotype
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. BMI of 23 kg/m² or higher, with a waist circumference exceeding 80 cm for females and 90 cm for males;
3. Weight stability for at least three months prior to the start of the study;
4. 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;
5. Baseline eating duration exceeding 12 hours per day;
6. Identified as either early or late chronotypes (Morningness-Eveningness Questionnaire)
Exclusion Criteria
2. Night shift workers;
3. Individuals with eating disorders;
4. Female participants who are breast-feeding, pregnant, or attempting to become pregnant;
5. Individuals currently participating in other weight-management programs or following other prescribed diet programs.
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Chinese University of Hong Kong
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Dai Zihan
Principal investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Department of Sports Science and Physical Education, The Chinese University of Hong Kong
Hong Kong, , China
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
NTEC-2025-189
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.