New program aims to boost recovery after heart bypass surgery
NCT ID NCT07392021
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a recovery program for people who have had coronary artery bypass surgery. The program includes education, activity guidance, and follow-up support from nurses. Researchers want to see if it helps patients feel more confident and recover better compared to standard care alone. About 60 adults in Thailand will take part.
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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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60 people
The number who actually took part.
- Started
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Aug 2025
- Expected to finish
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Aug 2026
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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20 years and older
- 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: * Thai patients undergoing elective first-time on-pump coronary artery bypass graft (CABG) surgery alone or combined with valve surgery * If age \>60 years, participants must pass cognitive screening using the 6-Item Cognitive Impairment Test (6-CIT) * New York Heart Association (NYHA) functional class I-III * Left ventricular ejection fraction (LVEF) \>30% * Independent in activities of daily living and able to perform the 6-minute walk test (6MWT) Exclusion Criteria: * Severe or acute comorbidities within 24 hours prior to surgery (e.g., chronic obstructive pulmonary disease, renal failure, acute myocardial infarction, severe arrhythmia) * Severe postoperative complications or unstable vital signs (e.g., major bleeding, significant arrhythmia, embolism, need for dialysis, extracorporeal membrane oxygenation) * Disability or limited ambulation or mobility assessed prior to hospital discharge * Failure of extubation within 3 days after surgery or requirement for reoperation
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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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Rajavithi Hospital, Ministry of Public Health, Thailand
Bangkok, Bangkok, 10400, Thailand
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Other studies related to the condition(s) this trial covers.
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