NCT07545330

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

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
32

participants targeted

Target at P25-P50 for not_applicable

Timeline
1mo left

Started Apr 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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 Progress51%
Apr 2026May 2026

Study Start

First participant enrolled

April 15, 2026

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

April 16, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 22, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 30, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 30, 2026

Last Updated

April 22, 2026

Status Verified

April 1, 2026

Enrollment Period

2 months

First QC Date

April 16, 2026

Last Update Submit

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

EXPERIMENTAL

Participants 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.

Other: Standardized Test Meal

Evening Meal Condition

EXPERIMENTAL

Participants 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.

Other: Standardized Test Meal

Interventions

The standardized test meal provided 50 g of carbohydrates of weighed portions of white bread and jam, served with 200 mL of water.

Evening Meal ConditionMorning Meal Condition

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

King Faisal University

Al-Ahsa, Eastern Province, 31982, Saudi Arabia

Location

Central Study Contacts

Wafa Alotaibi, PhD

CONTACT

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

Locations