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Not yet recruiting NCT07255807

Defining the Human Insulin Resistance Molecular Network; SIGNATURE

No phase Interventional Metabolic Health Insulin Sensitivity/Resistance

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Physical Inactivity, Hypercaloric High-Fat Diet.
Who it may be relevant to
Registry conditions: Metabolic Health, Insulin Sensitivity/Resistance. Basic parameters: 25 years — 55 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Denmark
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

sIgnatuRe: Defining the Human Insulin Resistance Molecular Network

Overview

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.

Detailed description

This intervention study aims to uncover the molecular mechanisms that underlie insulin resistance in otherwise healthy adults and to explore how short-term lifestyle changes may influence these mechanisms. Insulin resistance is a key feature in the development of type 2 diabetes and other metabolic diseases, but it does not arise uniformly across individuals. The overarching hypothesis is that insulin resistance has multiple underlying causes that differ between individuals, depending on genetic variation and modifiable lifestyle factors such as physical activity and diet.

A total of 80 healthy participants-40 males and 40 females aged between 25 and 55 years-will be recruited. All participants must have a body mass index (BMI) between 18 and 30 and meet strict inclusion and exclusion criteria to minimize confounding variables. Participants will be free of chronic disease, non-smokers, have limited alcohol intake, and not engage in high levels of physical activity. This controlled approach ensures a more accurate assessment of the variables under investigation.

At baseline, all participants will undergo comprehensive phenotyping, including assessments of habitual physical activity, dietary intake, glucose tolerance, and whole-body insulin sensitivity. This will allow the researchers to categorize sub-phenotypes of insulin resistance at both the physiological and molecular level.

Following baseline testing, 40 of the 80 participants will undergo one of two short-term interventions designed to stress metabolic pathways associated with insulin sensitivity:

* Reduced physical activity: Participants will significantly decrease their daily physical activity for 14 days. * High-fat diet: Participants will consume a hypercaloric high-fat diet for 3 consecutive days.

The aim of these interventions is to test how short-term negative lifestyle changes impact insulin action and related molecular markers, and whether these responses vary between individuals with different phenotypic and genetic profiles.

After the intervention period, selected metabolic tests will be repeated to assess changes in insulin sensitivity and molecular signaling. The primary outcome measure is whole-body insulin action, assessed using gold-standard physiological methods. Exploratory outcomes include identifying cellular and molecular mechanisms contributing to insulin resistance, and understanding the interaction between gene expression and lifestyle responses.

By combining deep phenotyping with short-term interventions, this study will generate new insights into the biological diversity of insulin resistance. Ultimately, this may contribute to the development of more individualized strategies for the prevention and treatment of metabolic diseases.

Interventions

  • Behavioral 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 an
  • Behavioral 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. Ba

Primary outcome measures

  • Whole-body insulin action [Time frame: Baseline characterization & immediately following intervention (either 14 days of physical inactivity or 3 days of hypercaloric high-fat diet)]
Secondary outcome measures (3)
  • Identification of proteins and posttranslational modification of proteins in blood as well as skeletal muscle and adipose tissue biopsies [Time frame: Baseline & immediately following the intervention (14 days of physical inactivity or 3 days of hypercaloric high-fat diet)]
  • Whole-Body Glucose Tolerance [Time frame: Baseline & immediately following the intervention (14 days of physical inactivity or 3 days of hypercaloric high-fat diet)]
  • Beta Cell Function [Time frame: Baseline & immediately following the intervention (14 days of physical inactivity or 3 days of hypercaloric high-fat diet)]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Basic science

Study locations

Denmark · 1 center
  • August Krogh Building — Copenhagen

Identifiers

NCT: NCT07255807 · SIGNATURE · NNF24OC0085866

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗