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Can your weight speed up aging? new study investigates

NCT ID NCT06511297

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study aims to understand how obesity and aging are connected by looking at blood markers in 650 young and older adults with or without obesity. Participants will provide blood samples and undergo imaging tests to measure biological age and fat distribution. The goal is to lay the groundwork for future treatments and lifestyle changes to prevent age-related diseases.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 650 people

The number the study aims to enrol. It can still change while the study runs.

Started

May 2025

Expected to finish

Jan 2036

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Community sample from eastern Austria.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Group 1 - Lean, young adults (n = 150) * Age 18 - 35 years * Body mass index (BMI) ≥ 18.5 and ≤ 24.9 kg/m2 (≥ 12 months) Group 2 - Overweight, young adults (n = 150) * Age 18 - 35 years * BMI ≥ 28kg/m2 (≥ 12 months) Group 3 - Lean, older adults (n = 150) * Age ≥ 60 years * BMI ≥ 18.5 and ≤ 24.9 kg/m2 (≥ 3 years) Group 4 - Overweight, older adults (n = 150) * Age ≥ 60 years * BMI ≥ 28 kg/m2 (≥ 3 years) * Subgroup A (n=75): with pre-existent cardiovascular disease defined as: history of myocardial infarction or evidence of coronary artery disease irrespective of revascularization status or history of ischemic or hemorrhagic stroke or presence of peripheral artery disease or heart failure with preserved ejection fraction (NYHA Class I-II). * Subgroup B (n=75): without pre-existent cardiovascular disease Group 5 - Nonagenerians Age ≥ 90 (n = 50) * Age ≥ 90 years * BMI ≥ 18.5 kg/m2 (≥ 3 years) Exclusion Criteria: Group 1 - Lean, young adults (n = 150) * Highly physical active (i.e. \> 5 times sporting activity / week with moderate to high intensity \[heart rate 140 - 200bpm\]) * Special diets (i.e. ketogenic diet and time-restricted eating) * Clinically significant metabolic or endocrine disorders * Claustrophobia * drug abuse, alcohol \> 15 drinks/week * Heart failure, cardiovascular disease, immunosuppressive therapies, chronic inflammatory diseases and active oncologic conditions * Metal implants that prohibit 3T MRI * Pregnancy or breastfeeding Group 2 - Overweight, young adults (n = 150) * Highly physical active (i.e. \> 5 times sporting activity / week with moderate to high intensity \[heart rate 140 - 200bpm\]) * Special diets (i.e. ketogenic diet and time-restricted eating) * Active anti-obesity treatment (e.g. glucagon-like peptide 1 (GLP-1) analogues, polyagonists, naltrexone and bupropion) * Clinically significant metabolic or endocrine disorders * Claustrophobia * drug abuse, alcohol \> 15 drinks/week * Heart failure, cardiovascular disease, immunosuppressive therapies, chronic inflammatory diseases and active oncologic conditions * Metal implants that prohibit 3T MRI * Pregnancy or breastfeeding Group 3 - Lean, older adults (n = 150) * Highly physical active (i.e. \> 5 times sporting activity / week with moderate to high intensity \[heart rate 140 - 200bpm\]) * Special diets (i.e. ketogenic diet and time-restricted eating) * Diabetes, overt hypo/hyperthyroidism * Claustrophobia * drug abuse, alcohol \> 15 drinks/week * Metal implants that prohibit 3T MRI * Known severe cardiovascular diseases (i.e. PAD IIa or higher, advanced heart failure = left ventricular ejection fraction (LVEF) \< 35% or NYHA Class III-IV) * No previous heart failure, cardiovascular disease, immunosuppressive therapies, chronic inflammatory diseases and active oncologic conditions up until the age of 35 years. * Life-threatening conditions with a life expectancy of less than 1 year or any other condition that would jeopardize proband safety/adherence while participating in this trial. Group 4 - Overweight, older adults (n = 150) * Special diets (i.e. ketogenic diet and time-restricted eating) * Diabetes, overt hypo/hyperthyroidism * Active anti-obesity treatment (e.g. GLP-1 analogues, polyagonists, naltrexone and bupropion) * Claustrophobia * drug abuse, alcohol \> 15 drinks/week * Metal implants that prohibit 3T MRI * No previous heart failure, cardiovascular disease, immunosuppressive therapies, chronic inflammatory diseases and active oncologic conditions up until the age of 35 years. * Life-threatening conditions with a life expectancy of less than 1 year or any other condition that would jeopardize proband safety/adherence while participating in this trial. Group 5 - "healthy" Nonagenerians Age ≥ 90 (n = 50) * Claustrophobia * Clinically significant cognitive impairment compromising study adherence * Metal implants that prohibit 3T MRI * Life-threatening conditions with a life expectancy of less than 1 year or any other condition that would jeopardize proband safety/adherence while participating in this trial.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Medical University of Graz

    RECRUITING

    Graz, Styria, Austria

  • Medical University of Vienna

    RECRUITING

    Vienna, State of Vienna, Austria

More trials for these conditions

Other studies related to the condition(s) this trial covers.