Virtual reality yoga may calm patients before a painful heart surgery step
NCT ID NCT07794709
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
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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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52 people
The number who actually took part.
- Started
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Aug 2024
- Finished
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Jan 2025
- 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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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * 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
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Prof. Dr. Cemil Tascioglu City Hospital
Istanbul, Istanbul, 34010, Turkey (Türkiye)
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