Inter-Individual Variability in Early Diet-Induced Thermogenesis After a Standardized Meal
1 other identifier
interventional
30
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jun 2026
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
First Submitted
Initial submission to the registry
May 13, 2026
CompletedFirst Posted
Study publicly available on registry
May 28, 2026
CompletedStudy Start
First participant enrolled
June 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2027
May 28, 2026
May 1, 2026
1 year
May 13, 2026
May 27, 2026
Conditions
Keywords
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
EXPERIMENTALHealthy 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.
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.
Eligibility Criteria
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
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- 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