Can heart surgery rehab move from hospital to home?
NCT ID NCT07811102
First seen Sep 09, 2026 · Last updated Sep 10, 2026 · Updated 1 time
Summary
Researchers are testing whether a hybrid cardiac rehabilitation programme can help adults recover after heart surgery. Participants start with two weeks of supervised exercise at the hospital, then continue training at home for six weeks using heart-rate monitors, a cloud care platform, weekly phone calls and text messages. The trial compares this approach with standard centre-based rehabilitation, which involves eight weeks of supervised sessions at the hospital. The main measure is change in peak oxygen uptake, a marker of fitness, after eight weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- hybrid cardiac rehabilitation, a programme that starts supervised exercise in hospital and continues at home with heart-rate monitoring and remote support
- What this could lead to
- If it works, patients recovering from heart surgery could complete rehabilitation at home with remote monitoring instead of attending hospital for every session.
- What could go wrong
- This is a small pilot study of 30 people, so it can only estimate whether the approach is worth testing in a larger trial. Home-based exercise may not suit everyone, and remote supervision may not match in-person care.
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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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30 people
The number who actually took part.
- Started
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Jun 2023
- Finished
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Mar 2025
- 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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20 to 75 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 * Aged 20 to 75 years. * Admitted to the department of cardiovascular surgery and undergoing cardiac surgery during the index admission. * Meeting the indications for cardiac rehabilitation. * Classified as low risk (Class B) for exercise training according to the 2013 American Heart Association exercise standards, that is, clinically stable coronary artery disease, valvular heart disease, congenital heart disease, cardiomyopathy, or an abnormal exercise test not reaching high-risk criteria. * Able to self-monitor exercise intensity. Exclusion Criteria * An irreversible condition causing exercise intolerance or limiting exercise capacity. * Persistent atrial fibrillation or non-sustained ventricular tachycardia within the preceding six months, an implanted defibrillator, or any other rhythm that could compromise the reliability of home heart-rate recording. * Hypertrophic cardiomyopathy or recent myocarditis. * New York Heart Association class III or IV; angina or ischaemic electrocardiographic change during moderate-intensity exercise; a fall in systolic blood pressure during exercise; non-sustained ventricular tachycardia; previous cardiac arrest; or any condition judged by the physician to be potentially life-threatening. * During the study, reported adverse symptoms or escalation of exercise-training risk to Class C or D, including suspected angina, abnormal dyspnoea, vomiting or syncope, or an emergency department visit or readmission. * Unable to operate the communication and exercise applications independently. * Declined to take part in testing.
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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
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Cheng Hsin General Hospital
Taipei, 11220, Taiwan
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