Pre-surgery exercise program may help high-risk heart patients leave the hospital sooner
NCT ID NCT07725887
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
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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
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 90 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Bezmialem Vakif University
RECRUITINGIstanbul, Eyupsultan, Turkey (Türkiye)
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