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Which exercise best trims belly fat and heart risk?

NCT ID NCT00917917

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 03, 2026 · Last updated Aug 04, 2026 · Updated 1 time

Summary

This trial tests whether the type of physical activity—resistance, endurance, or a mix—combined with a low-calorie diet can reduce belly fat and cardiovascular risk in people with metabolic syndrome. Adults aged 50-70 with metabolic syndrome are randomly assigned to one of three exercise groups, all following the same restrictive diet. After an initial training period, participants follow the program at home and are monitored for a year. The main goal is to see which exercise approach most effectively shrinks abdominal circumference, a key marker of metabolic syndrome.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
A combined program of physical activity (resistance, endurance, or both) and a restrictive diet (500-700 kcal/day)
What this could lead to
If successful, this could identify the most effective type of exercise to pair with diet for reducing belly fat and cardiovascular risk in people with metabolic syndrome, potentially improving long-term health outcomes.
What could go wrong
The trial is relatively small and the results may not apply to everyone. Long-term adherence to diet and exercise is often challenging, and the benefits may diminish once participants return to their normal routines.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

150 people

The number who actually took part.

Start date

May 2009

Finished

Oct 2011

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.

Ages

50 to 70 years

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: * 50-70 years old from both sexes * with metabolic syndrome * affiliated to a social security system * able to practice maximal physical exercises based on VO2 max * able to sign inform consent Exclusion Criteria: * recent (6 month) major health conditions and patients with recurrent health problems (1 per year) * patients who are not capable to perform VO2 max without abnormalities * dyserection treated patients * patients with insufficient comprehensive ability to feel questionnaire and/or to change habits

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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.

Contacts and locations

Locations

  • CHU Clermont-Ferrand

    Clermont-Ferrand, 63003, France

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