Effect of Circadian Timing of a Standardized Meal on Postprandial Glucose Response in Healthy Adults
1 other identifier
interventional
32
1 country
1
Brief Summary
This randomized crossover study aims to investigate the effect of circadian timing of a standardized meal (morning versus evening consumption) on postprandial glucose response in healthy adults. Postprandial glucose will be assessed using the incremental area under the curve (iAUC) over 120 minutes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 15, 2026
CompletedFirst Submitted
Initial submission to the registry
April 16, 2026
CompletedFirst Posted
Study publicly available on registry
April 22, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 30, 2026
April 22, 2026
April 1, 2026
2 months
April 16, 2026
April 16, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Incremental Area Under the Curve (iAUC) for Postprandial Glucose
The primary objective of this study is to investigate the effect of circadian timing of a standardized test meal (morning versus evening consumption) on postprandial glucose response in healthy adults, assessed as the incremental area under the curve (iAUC) for capillary blood glucose over 120 minutes following meal consumption
Baseline to 120 minutes after consumption of the standardized test meal
Secondary Outcomes (3)
Peak Postprandial Glucose (Morning vs Evening)
Baseline to 120 minutes after consumption of the standardized test meal
Time to Peak Glucose (Morning vs Evening)
Baseline to 120 minutes after consumption of the standardized test meal
Postprandial Glucose Profile (Morning vs Evening)
Baseline, 15, 30, 60, 90, and 120 minutes after consumption of the standardized test meal
Other Outcomes (3)
Night Eating Behavior
Baseline
Sleep Duration and Quality
Baseline
Chronotype
Baseline
Study Arms (2)
Morning Meal Condition
EXPERIMENTALParticipants will consume a standardized test meal in the morning following an overnight fasting period of at least 8 hours. Postprandial glucose will be measured over 120 minutes.
Evening Meal Condition
EXPERIMENTALParticipants will consume the same standardized test meal in the evening following a standardized fasting period of at least 8 hours prior to the test meal. Postprandial glucose will be measured over 120 minutes.
Interventions
The standardized test meal provided 50 g of carbohydrates of weighed portions of white bread and jam, served with 200 mL of water.
Eligibility Criteria
You may qualify if:
- Healthy adults aged 18 years and older
- Able and willing to provide informed consent
- Able to comply with study procedures
You may not qualify if:
- Diagnosis of diabetes or any metabolic disorder affecting glucose regulation
- Use of any medications
- Pregnant or breastfeeding women
- Night shift workers or individuals with irregular sleep patterns
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- King Faisal Universitylead
- Saudi Food and Drug Authoritycollaborator
Study Sites (1)
King Faisal University
Al-Ahsa, Eastern Province, 31982, Saudi Arabia
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 16, 2026
First Posted
April 22, 2026
Study Start
April 15, 2026
Primary Completion (Estimated)
May 30, 2026
Study Completion (Estimated)
May 30, 2026
Last Updated
April 22, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share
De-identified individual participant data (IPD) collected in this study will not be made publicly available. Data will be used for research purposes by the study investigators only