Walk your way to recovery: early exercise after bypass shows promise

NCT ID NCT07230561

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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 Results may not be published yet.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
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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 ยท Last updated Jun 27, 2026

Summary

This study tested whether a structured early exercise program helps people recover better after coronary artery bypass surgery. Forty adults who had their first bypass surgery were split into two groups: one received standard hospital care plus supervised exercise starting within 24 hours, and the other received standard care only. The exercise group did 30-minute sessions twice a day for 5 days, including walking, cycling, and light strength training. Researchers measured fitness, muscle strength, quality of life, and mood to see if early exercise leads to a faster and better recovery.

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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

40 people

The number who actually took part.

Started

Jul 2024

Finished

Jan 2025

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

40 to 85 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: * age between 40 and 85 years; * undergoing first-time CABG surgery; * no diagnosed psychiatric disorders or musculoskeletal diseases and did not require any assistive mobility devices; * ability to communicate in Mandarin or Taiwanese; * agreed to participate and provided written informed consent after receiving a comprehensive explanation of this trial. Exclusion Criteria: * preoperative use of continuous 24-hour nitroglycerin infusion or inotropic agents; * undergoing emergency cardiac surgery or requiring admission to the intensive care unit preoperatively; * occurrence of major intraoperative complications (e.g., major hemorrhage, stroke, requirement for resuscitation, or severe delirium).

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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

  • Far Eastern Medical Foundation Far Eastern Memorial Hospital

    New Taipei City, 220, Taiwan

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Other studies related to the condition(s) this trial covers.