Pre-surgery exercise program may help high-risk heart patients leave the hospital sooner

NCT ID NCT07725887

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Recruitment status, easiest to join first

Recruiting now This study
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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.
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Paused for now. It may or may not start again.
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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 Results may not be published yet.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)

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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
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Status unknown
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First seen Jul 24, 2026 · Last updated Jul 24, 2026

Summary

This trial tests whether a structured physiotherapy program started at least two days before coronary artery bypass grafting (CABG) and continued after surgery can improve recovery in high-risk patients. Participants are adults scheduled for elective CABG who meet at least three high-risk criteria, such as low heart function, multiple blocked arteries, or older age. The study compares the pre-and-post-surgery program to the same program given only after surgery, with the main goal of measuring hospital length of stay.

What this could mean

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

Active substance
a structured inpatient physiotherapy program including breathing exercises, incentive spirometry, bronchial hygiene, progressive mobilization, and postural exercises
What this could lead to
If it works, starting physiotherapy before surgery could shorten hospital stays and improve recovery for high-risk heart bypass patients.
What could go wrong
This is a single-center trial with 100 participants, so results may not apply broadly. The program adds extra effort before surgery, which some patients may find difficult.

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

About 100 people

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

Started

Jul 2026

Expected to finish

Jan 2027

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.

Ages

18 to 90 years

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 to undergo elective coronary artery bypass grafting (CABG). * High-risk patients meeting at least three of the following criteria: Left ventricular ejection fraction (LVEF) \<40%. Three-vessel coronary artery disease. More than two comorbidities. History of smoking. Age \>65 years. \- Able and willing to provide written informed consent. Exclusion Criteria: * Planned redo CABG surgery. * Severe neurological or orthopedic conditions limiting mobilization. * Severe cognitive impairment. * Hemodynamic instability. * Contraindications to mobilization or exercise. * Inability to complete at least two days of the preoperative physiotherapy program.

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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

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  1. The places running it

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  2. The official record

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Contacts and locations

Locations

  • Bezmialem Vakif University

    RECRUITING

    Istanbul, Eyupsultan, Turkey (Türkiye)

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