Could a personal playlist calm nerves during heart surgery?
NCT ID NCT07786961
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This trial tests whether listening to a personalized music playlist during coronary interventional procedures can reduce anxiety and pain. About 208 adults with acute coronary syndrome will be randomly assigned to either standard care or standard care plus music through wireless earphones throughout the procedure. Researchers will measure anxiety levels, pain, blood pressure, heart rate, and oxygen saturation to see if music makes a difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- personalized music playlist delivered via wireless earphones during the procedure
- What this could lead to
- If effective, this simple, drug-free approach could become a standard addition to heart procedures, easing anxiety and pain without extra medication.
- What could go wrong
- The trial is relatively small and open-label, so results may be influenced by patient expectations. Music may not meaningfully reduce anxiety or pain for everyone.
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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About 208 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2029
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 to 80 years
- 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.
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: * age \>18 years; * provision of written informed consent and ability to understand the informed consent form. Exclusion Criteria: * patients with ST-segment elevation myocardial infarction (STEMI); * patients with very-high-risk non-ST-segment elevation myocardial infarction (NSTEMI), as classified according to the 2023 European Society of Cardiology (ESC) Guidelines; * patients in cardiogenic shock; * presence of hearing impairment or deafness, assessed through clinical history; * patients unable to express their musical preferences; * patients with resuscitated cardiac arrest; * use of antipsychotic medications, assessed through clinical history; * history of epilepsy, assessed through clinical history.
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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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SS Annunziata Hospital, Sassari
Sassari, Sardinia, 07100, Italy
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