NCT07610759

Brief Summary

This study aims to characterize how individuals differ in their metabolic response to food intake, specifically focusing on early diet-induced thermogenesis (DIT). DIT refers to the increase in energy expenditure that occurs after eating and reflects the body's metabolic response to processing nutrients. Healthy adult participants will complete a single laboratory visit under standardized conditions. Resting metabolic rate will first be measured, followed by consumption of a standardized liquid meal (550 kcal). Energy expenditure will then be continuously monitored for 3 hours using indirect calorimetry. The primary objective is to quantify inter-individual variability in early postprandial thermogenesis. Rather than estimating total daily energy expenditure, this study focuses on the early metabolic response following meal ingestion. Findings will improve understanding of differences in metabolic efficiency between individuals and support future research in metabolism and personalized nutrition.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
12mo left

Started Jun 2026

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 Progress4%
Jun 2026Jun 2027

First Submitted

Initial submission to the registry

May 13, 2026

Completed
15 days until next milestone

First Posted

Study publicly available on registry

May 28, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

June 1, 2026

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2027

Last Updated

May 28, 2026

Status Verified

May 1, 2026

Enrollment Period

1 year

First QC Date

May 13, 2026

Last Update Submit

May 27, 2026

Conditions

Keywords

Diet-induced thermogenesisPostprandial metabolismEnergy expenditureMetabolic variabilityIndirect calorimetryStandardized meal

Outcome Measures

Primary Outcomes (1)

  • Early Diet-Induced Thermogenesis Area Under the Curve

    Area under the curve for diet-induced thermogenesis over 180 minutes after consumption of the standardized liquid meal. DIT will be calculated as postprandial energy expenditure minus baseline resting energy expenditure and expressed as kcal/180 min.

    From meal completion to 180 minutes post-meal

Secondary Outcomes (5)

  • Mean Diet-Induced Thermogenesis

    From meal completion to 180 minutes post-meal

  • Peak Diet-Induced Thermogenesis

    From meal completion to 180 minutes post-meal

  • Time to Peak Diet-Induced Thermogenesis

    Time from completion of the standardized liquid meal to the maximum observed increase in energy expenditure, expressed in minutes.

  • Percent Increase in Energy Expenditure Above Baseline

    From meal completion to 180 minutes post-meal

  • Fat-Free Mass-Normalized Diet-Induced Thermogenesis

    From meal completion to 180 minutes post-meal

Study Arms (1)

Healthy Adult Participants

EXPERIMENTAL

Healthy adults (≥18 years) participating in a single laboratory visit. All participants undergo resting metabolic rate assessment, consume a standardized liquid meal (550 kcal), and complete continuous postprandial energy expenditure measurement using indirect calorimetry under controlled conditions.

Other: Standardized Liquid Meal

Interventions

Consumption of a standardized liquid meal (\~550 kcal) under controlled laboratory conditions, followed by continuous measurement of energy expenditure using indirect calorimetry for assessment of postprandial thermogenesis. The procedure is used for measurement purposes only and is not intended as a therapeutic intervention.

Also known as: Ensure®
Healthy Adult Participants

Eligibility Criteria

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

You may qualify if:

  • Adults aged ≥18 years
  • Stable body weight (±2 kg over the previous 3 months)
  • Generally healthy individuals
  • Ability to comply with study procedures, including fasting and remaining at rest - during measurements

You may not qualify if:

  • Use of medications known to affect metabolism (e.g., GLP-1 receptor agonists, systemic corticosteroids, uncontrolled thyroid disease)
  • Insulin-treated diabetes
  • Pregnancy or lactation
  • Acute illness at the time of testing
  • Inability to comply with pre-test requirements (e.g., fasting, avoiding caffeine, alcohol, or physical activity)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sylvan Adams Sport Science Institute

Tel Aviv, 6428607, Israel

Location

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Model Details: All participants undergo a single standardized protocol including baseline resting metabolic rate assessment, consumption of a standardized liquid meal, and continuous postprandial energy expenditure measurement under controlled laboratory conditions.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator - Professor

Study Record Dates

First Submitted

May 13, 2026

First Posted

May 28, 2026

Study Start

June 1, 2026

Primary Completion (Estimated)

June 1, 2027

Study Completion (Estimated)

June 1, 2027

Last Updated

May 28, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Locations