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NCT07786961Not yet recruiting

Music Medicine in Coronary Interventional Cardiology Procedures

Effects of Music Medicine in Patients Undergoing Coronary Interventional Cardiology Procedures

Source: ClinicalTrials.gov · Last updated 26 Aug 2026

Brief summary (registry, in English)

The purpose of the study is: to evaluate the effectiveness of a personalized Music Medicine intervention in patients undergoing invasive coronary interventional cardiology procedures. The study will compare patients who listen to a personalized music playlist through wireless earphones throughout the procedure with patients receiving standard care without music. The primary objective is to assess whether Music Medicine reduces state anxiety, measured using the State-Trait Anxiety Inventory (STAI-Y1). Secondary objectives are to evaluate its effects on access-site crossover, procedural pain, blood pressure, heart rate, and oxygen saturation. The study will also assess adverse reactions, withdrawals, patient satisfaction with the intervention, and, in the Music Medicine group, patients' perceived experience through a semi-structured qualitative interview. The study is designed as a prospective, single-center, open-label, randomized controlled trial with two parallel groups and a 1:1 allocation ratio, enrolling 208 participants. The question the study is trying to answer is: whether listening to a personalized music playlist during an invasive coronary interventional cardiology procedure, in addition to standard care, reduces state anxiety compared with standard care alone, and whether it also improves other relevant procedural outcomes, including pain, the need for access-site crossover, blood pressure, heart rate, and oxygen saturation, without interfering with routine clinical care

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
208 (estimated)
First submitted
20 Aug 2026
Start date
1 Sept 2026
Primary completion date
31 Aug 2029
Lead sponsor
Azienda Ospedaliero Universitaria di Sassari
NCT number
NCT07786961

What you commit to

  • Study type: Interventional
  • Planned participants: 208
  • From 1 Sept 2026 to the primary completion date, 31 Aug 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • use of antipsychotic medications, assessed through clinical history;

Other illness

  • 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;
  • presence of hearing impairment or deafness, assessed through clinical history;
  • patients with resuscitated cardiac arrest;
  • history of epilepsy, assessed through clinical history.

Other

  • patients in cardiogenic shock;
  • patients unable to express their musical preferences;

Who the study is looking for

  • age \>18 years;
  • provision of written informed consent and ability to understand the informed consent form.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
SS Annunziata Hospital, Sassari
Coordinator of this site? Confirm its status
SassariItalyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.