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Clinical Trials in Denmark / NCT07255807
Recruiting Not applicable

Defining the Human Insulin Resistance Molecular Network; SIGNATURE

NCT07255807 · tracked via the Priya Life Science Denmark tracker
Phase
Not applicable
Started
2026-01-09
Last updated
2026-08-17

Condition(s) studied

Metabolic HealthInsulin Sensitivity/Resistance

Investigational drug(s) / intervention(s)

Physical InactivityHypercaloric High-Fat Diet

Physical Inactivity: Participants assigned to the physical inactivity intervention will reduce their daily physical activity to fewer than 1,500 steps per day for 14 consecutive days. This strict limitation significantly decreases overall movement and muscle activity, mimicking a sedentary lifestyle. The aim is to assess the short-term effects of reduced physical activity on insulin sensitivity and related metabolic processes. Compliance will be monitored using activity trackers and daily logs. Baseline metabolic and physiological assessments will be repeated after the intervention to evaluate changes.

Hypercaloric High-Fat Diet: Participants assigned to the high-fat diet intervention will consume a hypercaloric diet rich in fat for 3 consecutive days. The diet is designed to significantly increase caloric intake and fat consumption beyond habitual levels to induce short-term metabolic stress. This intervention aims to assess how a brief period of high-fat overfeeding affects insulin sensitivity and related molecular pathways. Participants' dietary intake will be carefully controlled and monitored to ensure adherence. Baseline metabolic and physiological assessments will be repeated after the intervention to evaluate changes.

Study summary

The goal of this intervention study is to learn more about what causes insulin resistance in otherwise healthy adults, and how short-term changes in physical activity or diet may influence it. The study includes healthy male and female participants aged 25 to 55 years, who meet specific health criteria.

The main questions it aims to answer are:

Does the cause of insulin resistance vary between individuals due to their genes and lifestyle?

Can the investigators identify different types (sub-phenotypes) of insulin resistance at the molecular level?

Researchers will compare groups who either reduce their physical activity for 14 days or consume a high-fat diet for 3 days, to see how these changes affect insulin sensitivity and related biological markers.

Participants will:

* Complete a health screening and be assessed for eligibility
* Undergo baseline testing to measure insulin sensitivity, physical activity, diet, and metabolic health
* Be randomly assigned to one of two short-term interventions (14 days of reduced physical activity, or 3 days of a high-fat, high-calorie diet)
* Repeat selected tests after the intervention to assess changes

This study will help researchers better understand how lifestyle and biology interact in the development of insulin resistance, even in people who are otherwise healthy.

Eligibility

Sex
ALL
Min age
25 Years
Max age
55 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Age: 25-55 years * Body Mass Index (BMI): 18-30 kg/m² * Healthy (no diagnosed chronic diseases) * Able and willing to comply with study procedures Exclusion Criteria: * Smoking or nicotine use, current or within the past 5 years * Alcohol intake exceeding 10 units per week * Hemoglobin A1c (HbA1c) \> 48 mmol/mol (indicative of diabetes or prediabetes) * Chronic diseases (e.g., cardiovascular disease, diabetes, etc.) * Chronic medication use, including hormonal treatments * High physical activity levels (more than 3 hours per week of moderate to vigorous exercise) * Pregnancy or within 3 months postpartum * Breastfeeding or within 3 months of cessation * Abnormal routine blood markers (as defined in lab screening) * Blood donation within the past 2 months

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
August Krogh Building Copenhagen Denmark Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07255807 on ClinicalTrials.gov ↗ ← All trials in Denmark