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Prepping the body before heart surgery: could exercise shorten hospital stays?

NCT ID NCT07704086

Disease control Sponsor: Hospital Universitario 12 de Octubre Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 15, 2026 · Last updated Jul 16, 2026 · Updated 1 time

Summary

This trial tests whether a prehabilitation program — including exercise, education, and breathing techniques — helps people recover faster after planned heart surgery. The study enrolls adults scheduled for surgery for coronary artery disease, valve problems, or other heart conditions. Researchers measure functional capacity and quality of life after surgery, and track how long participants stay in the hospital.

What this could mean

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

Active substance
a prehabilitation program combining physical exercise, health education, and respiratory physiotherapy
What this could lead to
If it works, this program could help people recover faster after heart surgery, spend fewer days in the hospital, and feel better sooner.
What could go wrong
This is a small, early-stage trial, so results may not apply to all heart surgery patients. The program requires extra effort before surgery, and not everyone may benefit equally.

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

86 people

The number who actually took part.

Started

Jun 2024

Finished

Jul 2026

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 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Adults aged 18 years or older. * Scheduled for elective cardiac surgery for one or more of the following indications: * Coronary artery disease. * Valvular heart disease. * Chronic thromboembolic pulmonary hypertension. * Aortic disease. Exclusion Criteria: \- Cognitive impairment that prevents understanding the study procedures or completing the intervention.

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Conditions

The condition(s) this trial relates to.

aortic disorder chronic thromboembolic pulmonary hypertension coronary artery disorder heart valve disorder

As listed by the trial registrant

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

Aortic diseases Chronic thromboembolic pulmonary hypertension Coronary artery disease Valvular heart disease

Contacts and locations

Locations

  • Hospital Universitario 12 de Octubre

    Madrid, Madrid, 28041, Spain

  • Universidad Complutense de Madrid

    Madrid, Madrid, Spain

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