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Delayed Dinner InterventionNCT07109583

Impact of Dinner Timing on Human Behaviours and Health

A study testing Early dinner and Delayed dinner in people with Delayed Dinner Intervention, run by National Taiwan Normal University at 1 site in Taiwan.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The aim of this project is to investigate the impact of dinner timing on eating behaviors, physical activity and metabolic healthy in healthy adults Read more about this study

Who is it for?
Ages 20 to 50 yearsHealthy volunteers can take part
Conditions the study is for
Delayed Dinner Intervention
What is being tested?
Early dinner and Delayed dinner
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 siteTaiwan
Study dates
20 Aug 2025to 1 Jul 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 50 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • No regular exerciser in the last 3 months.
  • BMI between 18.5-27 kg/m².
  • Regular habit of eating three meals per day, with dinner consumed between 17:00 and 20:00.
  • No intentional weight change (>3%) in the past 3 months.
  • No special dietary practices (e.g., intermittent fasting).
  • Regular sleep (22:00-01:00), at least 6.5 hours per night.
  • Non-smoker and non-alcoholic.
  • Willing to maintain stable lifestyle and comply with protocol.

Who cannot join

  • Pregnancy, preparing for pregnancy or menopause.
  • Personal history of/existing diabetes, cardiovascular disease or metabolic diseases.
  • Diagnosed sleep disorders.
  • Taking medications influencing glucose metabolism.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Yung-Chih Chen contact

+886277496979

yc.chen@ntnu.edu.tw

Taiwan1 site, 1 recruiting
  • National Taiwan Normal University

    Taipei

    Recruiting

Other trials in Taiwan

About this study

Official title: Effects of Dinner Timing on Eating Behaviour, Physical Activity and Metabolic Health

The aim of this project is to investigate the impact of dinner timing on eating behaviors, physical activity and metabolic healthy in healthy adults

Read the detailed description

In the early dinner trial, participants will be required to eat dinner between 17:30 and 19:00 for a week. In the delayed dinner trial, participants will be required to eat dinner between 20:30 and 22:00 for a week. During the intervention, energy intake (3 days of weekday and 1 day of weekend), physical activity (7 days), glucose concentrations (7 days) and sleep (7 days) will be monitored continuously for both early and delayed dinner.

After intervention, body composition, cognition, food preference, metabolic health and resting metabolic rate will be measured.

Being tested
Early dinner, Delayed dinner
Keywords
Eating behaviour, Physical activity, Metabolic health
Medical subject headings
Feeding Behavior, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Early dinnerBehavioural

    Consume dinner between 17:30 and 19:00 for a week

  • Delayed dinnerBehavioural

    Consume dinner between 20:30 and 22:00 for a week

Study groups in NCT07109583
Study groupRoleWhat they receive
Early dinnerExperimentalConsume dinner between 17:30 and 19:00 for one week
Receives: Behavioral: Early dinner
Delayed dinnerExperimentalConsume dinner between 20:30 and 22:00 for one week
Receives: Behavioral: Delayed dinner

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Glucose responses

    Changes in blood glucose responses between early and delayed dinner intervention

    Measured: During 7 days of early dinner and 7 days of delayed dinner intervention

  2. Eating behaviour

    Meal choice (i.e., energy intake in kcal) between early and delayed dinner intervention

    Measured: During early dinner and delayed dinner intervention (3 days of weekday and 1 day of weekend)

Secondary outcomes (10)
  1. Sleep duration

    Changes in sleep duration between early and delayed dinner intervention using MotionWatch

    Measured: During 7 days of early dinner and 7 days of delayed dinner intervention

  2. Sleep quality

    Changes in sleep quality (efficiency, %) between early and delayed dinner intervention using MotionWatch

    Measured: During 7 days of early dinner and 7 days of delayed dinner intervention

  3. Physical activity level

    Changes in physical activity level (minutes) between early and delayed dinner intervention

    Measured: During 7 days of early dinner and 7 days of delayed dinner intervention

  4. Physical activity intensity

    Changes in physical activity intensity (%) between early and delayed dinner intervention using wearable product

    Measured: During 7 days of early dinner and 7 days of delayed dinner intervention

  5. Cognitive performance

    Changes in computerized cognitive performance (accuracy in %) after early and delayed dinner intervention

    Measured: Before and after early and delayed dinner intervention

  6. Food preference tests

    Changes in food preference after early and delayed dinner intervention

    Measured: Before and after early and delayed dinner intervention

  7. Resting resting metabolic rate

    Changes in resting metabolic rate (kcal) after early and delayed dinner intervention

    Measured: Before and after early and delayed dinner intervention

  8. Body composition

    Changes in body composition (fat mass in kg and percentage) after early and delayed dinner intervention using InBody

    Measured: Before and after early and delayed dinner intervention

  9. Blood pressure

    Changes in blood pressure (diastolic and systolic blood pressure in mmHg) after early and delayed dinner intervention

    Measured: Before and after early and delayed dinner intervention

  10. Pulse wave velocity

    Changes in pulse wave velocity (meter per second) after early and delayed dinner intervention

    Measured: Before and after early and delayed dinner intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Aug 2025
  2. Study start20 Aug 2025
  3. Primary completion1 Jul 2026 (estimated)
  4. Study completion1 Jul 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07109583
Sponsor's protocol ID
202203HM008-2
Status last verified
Jan 2026
First submitted
26 Jun 2025
Last updated
23 Jan 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Early dinner and Delayed dinner in people with Delayed Dinner Intervention, run by National Taiwan Normal University at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 23 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Yung-Chih Chen (+886277496979, yc.chen@ntnu.edu.tw), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Glucose responses (time frame: During 7 days of early dinner and 7 days of delayed dinner intervention). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jan 2026.

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