Meditation before heart surgery may lower stress hormones
NCT ID NCT07379944
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether listening to guided meditation audio can reduce stress and anxiety in people having open-heart surgery. About 72 adults will either receive meditation sessions or standard care. Researchers will measure stress hormones, blood sugar, and anxiety levels before and after surgery to see if meditation helps.
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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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About 72 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- 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 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 18 years or older * Scheduled to undergo open-heart surgery * ASA physical status I-II * First-time cardiac surgery * On-pump, median sternotomy technique planned * Mild to moderate intraoperative hypothermia protocol * No diagnosed psychiatric disorder * Not using psychotropic medications * No endocrine disorders affecting cortisol (e.g., Addison's disease, Cushing's syndrome) * Not taking corticosteroid medications * Glasgow Coma Score = 15 postoperatively * No perioperative complications that may interfere with participation * Able and willing to provide informed consent Exclusion Criteria: * Prolonged or complicated surgery * Withdrawal of consent at any stage * Postoperative altered consciousness (GCS \< 15) * Perioperative administration of corticosteroids * Severe intraoperative complications * Surgery cancelled or rescheduled * Hearing impairment preventing participation in auditory intervention * Any condition clinically judged by the investigator to interfere with study participation
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Gaziantep University
Gaziantep, Şehitkamil, 27310, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Heart bypass surgeons test which vein layout keeps grafts open
- Can a group program teach teens to cope before therapy starts?
- A soft patch that watches your heart beat in real time
- Could a Patient's playlist take the sting out of nerve testing?
- Zapping the ear: a new way to stop Post-Surgery heart rhythm problems?