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Recruiting NCT07109583

Impact of Dinner Timing on Human Behaviours and Health

No phase Interventional Delayed Dinner Intervention

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Early dinner, Delayed dinner.
Who it may be relevant to
Registry conditions: Delayed Dinner Intervention. Basic parameters: 20 years — 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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

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.

Interventions

  • Behavioral Early dinner
    Consume dinner between 17:30 and 19:00 for a week
  • Behavioral Delayed dinner
    Consume dinner between 20:30 and 22:00 for a week

Primary outcome measures

  • Glucose responses [Time frame: During 7 days of early dinner and 7 days of delayed dinner intervention]
  • Eating behaviour [Time frame: During early dinner and delayed dinner intervention (3 days of weekday and 1 day of weekend)]
Secondary outcome measures (10)
  • Sleep duration [Time frame: During 7 days of early dinner and 7 days of delayed dinner intervention]
  • Sleep quality [Time frame: During 7 days of early dinner and 7 days of delayed dinner intervention]
  • Physical activity level [Time frame: During 7 days of early dinner and 7 days of delayed dinner intervention]
  • Physical activity intensity [Time frame: During 7 days of early dinner and 7 days of delayed dinner intervention]
  • Cognitive performance [Time frame: Before and after early and delayed dinner intervention]
  • Food preference tests [Time frame: Before and after early and delayed dinner intervention]
  • Resting resting metabolic rate [Time frame: Before and after early and delayed dinner intervention]
  • Body composition [Time frame: Before and after early and delayed dinner intervention]
  • Blood pressure [Time frame: Before and after early and delayed dinner intervention]
  • Pulse wave velocity [Time frame: Before and after early and delayed dinner intervention]

Eligibility criteria

Inclusion criteria

  • 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.

Exclusion criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Crossover
Masking
Open label
Primary purpose
Basic science

Study locations

Taiwan · 1 center
  • National Taiwan Normal University — Taipei

Identifiers

NCT: NCT07109583 · 202203HM008-2

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗