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Getting heart surgery patients moving sooner may speed recovery

NCT ID NCT07276971

Symptom relief Sponsor: Hulya BULUT Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jul 23, 2026 · Updated 2 times

Summary

This study tested a safe early mobilization plan for 60 patients who had coronary artery bypass surgery. The plan included gentle activities like sitting up, deep breathing, and walking starting the day of surgery. The goal was to see if this approach could reduce dizziness, improve oxygen levels, and shorten hospital stays compared to usual care.

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

60 people

The number who actually took part.

Started

Oct 2023

Finished

Dec 2023

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 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: Hemodynamic stability, defined as: Resting heart rate \<110/min Mean arterial pressure between 60-110 mmHg Oxygen saturation (SpO₂) \>88% Receiving dopamine infusion ≤5 mcg/kg/min at the time of enrollment No auditory, speech, or visual impairments No neurological contraindications (e.g., cerebrovascular accident \[CVA\], ataxia, multiple sclerosis \[MS\]) No orthopedic contraindications that prevent mobilization (e.g., fractures or sequelae) Provided informed consent to participate in the study Age ≥18 years Able to speak Turkish Literate patients Exclusion Criteria: Requirement for intra-aortic balloon pump (IABP) support Postoperative cerebrovascular events High-dose inotropic drug infusion in the early postoperative period: Dopamine ≥10 mcg/kg/min Norepinephrine ≥0.5 mcg/kg/min Concurrent dopamine and norepinephrine infusion Severe arrhythmias preventing mobilization, including: Sinus tachycardia ≥120/min Rapid atrial fibrillation Ventricular tachycardia Ventricular fibrillation Advanced chronic obstructive pulmonary disease (COPD) or bronchiectasis Diagnosed anxiety disorders

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Conditions

The condition(s) this trial relates to.

coronary artery disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Coronary artery bypass graft Nursing

Contacts and locations

Locations

  • Guven Hospital

    Ankara, Turkey (Türkiye)

More trials for these conditions

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