Virtual reality yoga may calm patients before a painful heart surgery step

NCT ID NCT07794709

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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 Results may not be published yet.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
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Expanded access (paused)
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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.

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Status unknown
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First seen Aug 31, 2026 · Last updated Sep 01, 2026 · Updated 1 time

Summary

This trial tests whether virtual reality-based breathing yoga can reduce pain and anxiety in adults before chest tube removal after cardiac surgery. Participants are randomly assigned to either watch breathing yoga videos through VR glasses for 15-20 minutes before the procedure, or receive standard care. Researchers measure pain and anxiety levels before and after chest tube removal to see if the VR intervention helps.

What this could mean

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

Active substance
Virtual reality-based breathing yoga
What this could lead to
If it works, this could give cardiac surgery patients a drug-free way to reduce pain and anxiety during a stressful procedure.
What could go wrong
The trial is small and early, so results may not apply broadly. The intervention may not significantly reduce pain or anxiety compared to standard 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

52 people

The number who actually took part.

Started

Aug 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

18 to 70 years

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: * Aged 18-70 years * Underwent coronary artery bypass grafting or valve surgery * Willing to participate in the study * Mobilized and extubated on the second postoperative day * Able to communicate without cognitive, sensory, or verbal impairment * No diagnosed psychiatric disorder * No vertigo * No diagnosis of hypertension and not receiving antihypertensive treatment * Not receiving sedative or anxiolytic medication * No major intraoperative or postoperative complications, such as severe bleeding, nausea, or vomiting Exclusion Criteria: \- Remained intubated on the second postoperative day

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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

  • Prof. Dr. Cemil Tascioglu City Hospital

    Istanbul, Istanbul, 34010, Turkey (Türkiye)

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