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Simple breathing trick may help heart surgery patients sleep better

NCT ID NCT07470034

Symptom relief Sponsor: Sanko University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether adding a diaphragm release technique to standard cardiac rehabilitation could improve sleep quality and lung function in 30 patients who had coronary artery bypass surgery. One group received standard rehab plus the diaphragm release, while the other received standard rehab alone. Researchers measured breathing, sleep, muscle strength, and pain levels during recovery.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
diaphragm release technique
What this could lead to
If it works, this simple technique could help heart surgery patients sleep better and breathe easier during recovery.
What could go wrong
This is a very small, completed study with only 30 participants, so results may not apply to everyone. The technique is non-invasive and low-risk.

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

30 people

The number who actually took part.

Started

Aug 2025

Finished

Feb 2026

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 to 65 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 under 65 years * Undergoing minimally invasive coronary artery bypass graft (CABG) surgery * Hemodynamically stable * Ambulatory (able to walk) * Willing to participate in the study and provide written informed consent * Mini-Mental State Examination (MMSE) score ≥ 25 Exclusion Criteria: * History of cerebrovascular events (stroke, TIA) * Orthopedic problems preventing walking * Uncontrolled diabetes * Uncontrolled hypertension * Severe visual impairment * Other diseases limiting participation in exercise training (pulmonary, neurological, metabolic, etc.) * Verbal or auditory cooperation problems

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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.

Cardiac rehabilitation Coronary artery bypass

Contacts and locations

Locations

  • Sanko Unıversıty

    Gaziantep, şehitkamil, 27500, Turkey (Türkiye)

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