NCT06537401

Brief Summary

The purpose of this study is to understand how the body's response after a meal is influenced by insulin and sugar in the blood. The primary question this study seeks to address is what is the effect of reduced insulin sensitivity on postprandial metabolic flexibility to an oral glucose tolerance test. We will recruit 50 adults (ages 20-45; 50% female) who are otherwise healthy (no known clinical diagnosis) into our non-randomized crossover trial to determine the effect of changes in insulin sensitivity on metabolic response to feeding. Insulin sensitivity will be decreased using a three-day high-fat diet (HFD) with extra calories. Whole-body metabolism will be measured during a standard 75-gram oral glucose tolerance test (OGTT). Metabolic response to feeding (e.g. OGTT) will be compared before and after the HFD and compared with the control diet to understand the effect of decreased insulin sensitivity on the metabolic response to feeding. The role of biological sex as a moderator of the effect of increased insulin resistance on postprandial metabolic flexibility will also be investigated

Trial Health

57
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Trial Health Score

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

Enrollment
2

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Aug 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

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

August 1, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 5, 2024

Completed
7 days until next milestone

Study Start

First participant enrolled

August 12, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
Last Updated

August 26, 2025

Status Verified

August 1, 2025

Enrollment Period

5 months

First QC Date

August 1, 2024

Last Update Submit

August 21, 2025

Conditions

Keywords

MetabolismFeedingSubstrate OxidationMetabolic FlexibilityHigh Fat DietInsulin Sensitivity

Outcome Measures

Primary Outcomes (1)

  • Postprandial Metabolic Flexibility

    Mean difference respiratory exchange ratio during an oral glucose tolerance test following a high fat diet

    3 Days

Study Arms (1)

Hypercaloric, High Fat Diet

EXPERIMENTAL

For three calendar days participants will be asked to track all foods they eat and beverages they drink (habitual diet) in a mobile application. Following the three days following the habitual diet, participants will consume 165% of their estimated daily energy needs with 65% of those calories coming from fat.

Behavioral: Hypercaloric, High Fat Diet

Interventions

Participants will select meals from a list of sample breakfast, lunch, and dinner options from grocery stores. Typical intake will be estimated as 160-170% of resting metabolic rate, which will then be multiplied by 1.65 as the target calorie intake for the HFD. Target fat intake will be 65% of the HFD calorie target. To ensure participants will achieve the desired calorie and fat intake, they will also be provided with pre-made nutrient shakes and half-and-half. Participants will supplement their food intake with one to three shakes per day for each of the three days, depending on the fat and calorie content of the foods they select. They will be asked to add half-and-half equally between across the shakes.

Hypercaloric, High Fat Diet

Eligibility Criteria

Age20 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Males or Females between the ages of 20 and 45 years
  • Body mass index (BMI) of 18.5-29.9 kg/m2
  • Low risk for medical complications as determined by physical activity readiness questionnaire (PARQ).
  • Low risk for food insecurity via the Hunger Vital Sign screener

You may not qualify if:

  • Currently taking any antioxidant supplementation, prescription non-steroidal anti- inflammatory drugs, antibiotics, steroids, probiotics, medications for management of cholesterol, diabetes, body weight/obesity, or are undergoing transgender hormone therapy.
  • Currently pregnant (verified by urine pregnancy test)
  • Any history of disordered eating (i.e., anorexia nervosa, bulimia nervosa, binge eating disorder, etc.) or high risk for disordered eating via validated questionnaire (SCOFF)
  • Any history of gastrointestinal diseases (i.e., gastroesophageal reflux disease, irritable bowel syndrome, Celiac disease, Crohn's disease, or lactose intolerance)
  • Allergies to wheat or gluten, milk, soy, tree nuts (e.g., almonds, walnuts, pecans), or peanuts.
  • Followed a ketogenic diet within the last three months
  • Instructed by a medical provided to avoid a high-fat diet due to cardiovascular disease risk.
  • Cardiorespiratory fitness (VO2max) greater than the 90th percentile for age and sex

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

George Washington University School of Public Health

Washington D.C., District of Columbia, 20052, United States

Location

MeSH Terms

Conditions

ObesityInsulin ResistanceGlucose Intolerance

Interventions

Diet, High-Fat

Condition Hierarchy (Ancestors)

OverweightOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and SymptomsHyperinsulinismGlucose Metabolism DisordersMetabolic DiseasesHyperglycemia

Intervention Hierarchy (Ancestors)

DietNutritional Physiological PhenomenaDiet, Food, and NutritionPhysiological Phenomena

Study Officials

  • Matthew D Barberio, PhD

    George Washington University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Model Details: Non-Randomized Crossover
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor, Department of Exercise and Nutrition Science

Study Record Dates

First Submitted

August 1, 2024

First Posted

August 5, 2024

Study Start

August 12, 2024

Primary Completion

December 31, 2024

Study Completion

December 31, 2024

Last Updated

August 26, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

Locations