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Which exercise is best after a heart attack? study seeks answers

NCT ID NCT04190394

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study compared two types of exercise training for people who had a heart attack: continuous moderate exercise and intermittent high-intensity exercise. One hundred participants completed an 8-week program, and researchers used ultrasound to measure changes in heart function. The goal was to see if one type of exercise improves heart muscle movement more than the other.

What this could mean

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

Active substance
exercise training program
What this could lead to
If successful, this could help doctors choose the best type of exercise program for heart attack recovery.
What could go wrong
This is a small, completed study with 100 participants, so results may not apply to everyone. It compares two exercise types, not a new drug or treatment.

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

100 people

The number who actually took part.

Started

Mar 2020

Finished

Jul 2023

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

18 to 75 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: * patient must have given free informed consent and signed the consent form * patient must be affiliated to or be covered by a health insurance scheme. * patient must be an adult aged ≥ 18 to ≤ 75 years old. * Patient must have had a first episode of myocardial infarction treated via medical treatment or by revascularization like a percutaneous transluminal angioplasty (only if the patient has had complete revascularization) at least 6 weeks previously. Exclusion Criteria: * The patient is participating in another intervention study or has taken part in another interventional study in the past 3 months * The patient is in an exclusion period determined by a previous study * The patient is often under curatorship, tutorship or advisorship. * It is impossible to give the patient clear information * The patient refuses to sign the consent form * The patient is pregnant, about to give birth or breastfeeding * The patient has a contraindication for retraining * The patient has a prosthetic heart valve * The patient has severe valve disorder * The patient requires cardiac stimulation * The patient has an automatic implantable defibrillator * The patient has sinus tachycardia, sinus bradycardia or sinus arrhythmia * The patient has non-controlled high blood pressure * The patient has a ventricular ejection fraction \< 45% * The patient has already participated in a cardiac rehabilitation program less than a year before * The patient has a relapse of myocardial ischaemia during the study

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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

  • Clinique Lavarin, Centre de Rééducation Cardiaque,1 Rue Mère Térésa,

    Avignon, Vaucluse, 84000, France

  • Nîmes University Hospital

    Nîmes, Gard, 30000, France

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