AzTrials
AzTrials

Acute Coronary SyndromeMUSICORNCT07786961

Music Medicine in Coronary Interventional Cardiology Procedures

A study testing Music Medicine intervention in people with Acute Coronary Syndrome, run by Azienda Ospedaliero Universitaria di Sassari at 1 site in Italy.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The purpose of the study is: to evaluate the effectiveness of a personalized Music Medicine intervention in patients undergoing invasive coronary interventional cardiology procedures. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Acute Coronary Syndrome
What is being tested?
Music Medicine intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
208 participants
Where
1 siteItaly
Study dates
1 Sep 2026to 31 Oct 2029
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

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

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Valentina Micheluzzi, PhD contact

+39 3401753630

valentina.micheluzzi@aousassari.it

Italy1 site
  • SS Annunziata Hospital, Sassari

    Sassari, Sardinia, 07100

    Valentina Micheluzzi, PhD, +39 3401753630, valentina.micheluzzi@aousassari.it

Other trials in Italy

About this study

Official title: Effects of Music Medicine in Patients Undergoing Coronary Interventional Cardiology Procedures

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

Read the detailed description

Coronary interventional cardiology procedures include invasive percutaneous procedures such as coronary angiography and percutaneous coronary intervention. These procedures are performed in the cardiac catheterization laboratory and may last approximately 30 to 120 minutes, depending on the clinical situation and procedural complexity. Although they are routinely performed and are essential for the diagnosis and treatment of coronary artery disease, the procedural environment, arterial access, manipulation of catheters and guidewires, and uncertainty related to the intervention may be associated with anxiety, discomfort, and pain.

Procedure-related anxiety may have both psychological and physiological consequences. Activation of autonomic and neuroendocrine stress responses may influence cardiovascular parameters and may also increase the perception of procedural pain. Pain itself may have procedural implications. In particular, during transradial procedures, pain and discomfort may contribute to radial artery spasm, which can make catheter manipulation more difficult and, in some cases, require a change to another arterial access site.

Pharmacological strategies, including analgesic and sedative medications, may be used when clinically indicated to manage anxiety, discomfort, and pain during invasive cardiac procedures. However, complementary non-pharmacological approaches may provide additional support without replacing or modifying standard clinical treatment.

Music Medicine refers to the structured use of music within healthcare by trained healthcare professionals according to a defined protocol. In this study, Music Medicine is considered a complementary, patient-centered intervention intended to make the procedural experience more comfortable while preserving all aspects of routine medical and nursing care. Previous research in cardiovascular settings has suggested that music-based interventions may have beneficial effects on psychological distress, anxiety, pain, blood pressure, heart rate, and overall patient well-being. Music has also been studied during angiographic and cardiac catheterization procedures, but evidence concerning a fully personalized music intervention delivered throughout coronary interventional procedures remains limited.

MUSICOR is a prospective, single-center, open-label, randomized controlled study conducted at the Cardiac Catheterization Laboratory of the University Hospital of Sassari, Italy. A total of 208 participants undergoing invasive coronary interventional cardiology procedures will be enrolled and randomly allocated in a 1:1 ratio to either a Music Medicine group or a standard-care group.

Participants will be recruited consecutively during hospitalization. After enrollment and completion of baseline study procedures, participants will be assigned to one of the two study groups using a computer-generated random allocation sequence. The randomization sequence will be prepared by a data manager who is not involved in participant recruitment or clinical management. Allocation will be implemented using sequentially numbered, opaque, sealed envelopes in order to prevent advance knowledge of group assignment. Because participants in the intervention group will listen to music and healthcare professionals must manage the music-delivery system, blinding of participants and clinical staff is not feasible.

### Music Medicine Intervention

Participants assigned to the Music Medicine group will receive a personalized music intervention in addition to routine clinical care.

Before the coronary procedure, a healthcare professional trained in Music Medicine and in the research protocol will discuss the participant's musical preferences. Rather than prescribing a predetermined genre of music, the intervention is centered on the individual participant's preferences. Participants will be encouraged to select music that they personally associate with relaxation, calmness, reassurance, or enjoyment.

The participant may identify individual songs directly or may initially indicate preferred artists, genres, or types of music from which appropriate tracks can then be selected. The final choice of music will remain patient-centered. The participant will also be able to determine the sequence in which the selected tracks are played.

A personalized playlist will then be prepared according to the participant's selections. Before the coronary procedure begins, trained healthcare personnel will verify the audio system, prepare the playlist, and position wireless earphones. Playback will begin before or at the start of the invasive procedure and will continue throughout the procedure according to the predefined sequence selected by the participant.

The audio system is designed so that the use of music does not prevent communication between the participant and the healthcare team. Medical and nursing staff will remain able to communicate with the participant during the procedure through the study communication system whenever clinically necessary. Participants will therefore remain in contact with the clinical team and able to communicate needs or discomfort during the intervention.

The music intervention will not determine or modify any diagnostic, interventional, pharmacological, or therapeutic decision. The arterial access site, procedural technique, use of medications, administration of analgesia or sedation, and any additional treatment will continue to be determined exclusively by the treating physicians according to the participant's clinical condition and routine clinical practice.

The Music Medicine intervention may be discontinued at any time if requested by the participant or if interruption is considered necessary for clinical or procedural reasons. At completion of the coronary procedure, the earphones will be removed and the disposable components of the system will be discarded and replaced before use with another participant.

### Standard-Care Group

Participants assigned to the control group will undergo the coronary procedure according to the routine clinical and nursing care provided in the Cardiac Catheterization Laboratory of the University Hospital of Sassari.

Standard care includes routine preparation for the procedure, continuous clinical monitoring, monitoring of vital signs, medical and nursing assistance throughout the procedure, and administration of pharmacological treatment, including analgesic and/or sedative medication when clinically indicated.

The arterial access site, procedural strategy, interventional techniques, and any additional treatment will be selected according to the participant's clinical condition, physician judgment, and current clinical practice.

Participants in the standard-care group will not wear study earphones and will not listen to either a personalized playlist or other music as part of the study during the coronary procedure. Apart from the Music Medicine intervention, clinical care will be comparable between the two study groups.

### Study Assessments and Data Collection

The study includes a baseline assessment before the coronary procedure and a post-procedure assessment after completion of the intervention.

At baseline, sociodemographic and clinically relevant information will be recorded to characterize the study population. These data include demographic characteristics and selected cardiovascular and clinical variables, such as cardiovascular risk profile, current medical therapy, left ventricular function, body mass index, functional status, and comorbidity burden.

Study assessments will examine psychological, procedural, and physiological aspects of the participant's experience before and after the coronary procedure. The study will also document procedural information relevant to arterial access and any need to change the initially selected access site.

All study data will be entered into a dedicated electronic database using the REDCap platform.

### Patient Experience Component

In addition to the quantitative comparison between the two randomized groups, MUSICOR includes a qualitative component intended to provide a more detailed understanding of how participants experience personalized music during an invasive coronary procedure.

Participants who receive the Music Medicine intervention will be asked about their satisfaction with the intervention. They will also take part in an individual semi-structured interview conducted after the coronary procedure, at a time compatible with their clinical condition.

The interview will be conducted by a psychologist using an open-ended and non-directive approach and will be audio-recorded for subsequent transcription and analysis. Participants will be encouraged to describe the experience in their own words.

The interview will explore several aspects of the intervention, including expectations before the procedure, the meaning attributed to listening to music, perceived emotional and physical effects, the importance of being able to personalize the playlist, comfort and acceptability of the earphones, communication with healthcare professionals while listening to music, perception of the catheterization laboratory environment and passage of time, and any positive, negative, or neutral aspects of the experience.

Participants will also be invited to describe whether they would choose to use personalized music again during a similar future procedure and to provide suggestions regarding music selection, playlist preparation, listening methods, or communication with clinical staff.

The qualitative component is intended to complement the quantitative findings by identifying aspects of acceptability, feasibility, and patient experience that may not be fully captured through standardized measurements.

### Analysis

Quantitative analyses will follow an intention-to-treat approach. Baseline characteristics of the study groups will be summarized using descriptive statistics, and the comparability of the randomized groups will be examined using appropriate statistical tests.

For repeatedly assessed continuous variables, the principal analysis will consider both treatment group and time, as well as the interaction between treatment group and time, in order to determine whether changes occurring across the coronary procedure differ between participants receiving Music Medicine and those receiving standard care. Between-group estimates will be reported with measures of statistical uncertainty and effect size where appropriate. Additional regression analyses may be performed to examine relationships between clinical or demographic characteristics and study variables.

The qualitative interviews will be analyzed using inductive qualitative content analysis. Transcripts will be read repeatedly and relevant meaning units will be identified, condensed, coded, and progressively organized into subcategories and descriptive categories. Where supported by the data, broader themes may also be identified.

The qualitative analysis will primarily focus on the manifest content of participants' accounts while also considering underlying meanings when clearly supported by the interview material. Analytical decisions and changes to the coding structure will be documented to promote transparency and traceability.

The integration of quantitative and qualitative information is intended to provide a more complete understanding of both the measurable effects of personalized Music Medicine and the way in which patients perceive and experience this intervention during coronary interventional cardiology procedures.

MUSICOR is therefore designed not only to determine whether personalized Music Medicine has measurable effects during invasive coronary procedures, but also to assess whether this approach is acceptable and practical within the cardiac catheterization laboratory environment. If the intervention proves beneficial and feasible, it could support the development of a simple, patient-centered complementary strategy that can be incorporated alongside established clinical care without interfering with medical decision-making or procedural management.

Being tested
Music Medicine intervention
Keywords
Music Medicine, Acute Coronary Syndrome, Percutaneous Coronary Intervention, Coronary Angiography
Medical subject headings
Acute Coronary Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Music Medicine interventionOther

    Also called Music Therapy

    The patient will listen to selected music with characteristics associated with relaxation, calmness, and personal enjoyment, with the aim of reducing anxiety and pain. A healthcare professional will prepare the playlist in the sequence selected by the patient and password-protect it on an MP3 device connected to Spotify. The patient will listen to the playlist through wireless earphones throughout the coronary interventional cardiology procedure.

Study groups in NCT07786961
Study groupRoleWhat they receive
Music Medicine armExperimentalPatients randomly allocated to the intervention group will listen to a personalized music playlist throughout the entire invasive cardiac procedure. The personalized playlist will be prepared as follows: a) On the day before the procedure, a healthcare professional trained in Music Medicine and in the study protocol will ask the patient which music they would like to listen to during the cardiac procedure. The healthcare professional will explain that the selected music should have characteristics associated with relaxation, calmness, and personal enjoyment, with the aim of reducing anxiety and pain. The patient will listen to the playlist through wireless earphones. b) The healthcare professional will prepare the playlist in the sequence selected by the patient and password-protect it on an MP3 device connected to Spotify. c) Before the procedure begins, a healthcare professional trained in Music Medicine and in the study protocol will place the earphones on the patient, access th
Receives: Other: Music Medicine intervention
Standard Care ArmNo interventionPatients randomized to the control group will undergo the coronary cardiac procedure according to the standard clinical care routinely provided in the Cardiac Catheterization Laboratory of the University Hospital of Sassari (AOU Sassari). Standard care will include the usual preparation of the patient for the procedure, clinical and vital-sign monitoring, nursing and medical care throughout the procedure, and administration of pharmacological therapies, including analgesics and/or sedatives when clinically indicated, according to the operator's judgment and current clinical practice. The arterial access site, technical aspects of the procedure, and any additional treatment will be determined exclusively on the basis of the patient's clinical condition and routine care procedures. During the procedure, patients in the standard-care group will not use earphones and will not listen to either a personalized music playlist or any other music.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mean Change From Baseline in State Anxiety Score Assessed by the State-Trait Anxiety Inventory (STAI-Y1)

    State anxiety will be assessed using the State-Trait Anxiety Inventory, State subscale (STAI-Y1). The STAI-Y1 consists of 20 items rated on a 4-point Likert scale. The total score ranges from 20 to 80, with higher scores indicating greater state anxiety. The outcome will be expressed as the mean change in STAI-Y1 total score from baseline to immediately after the coronary interventional cardiology procedure.

    Measured: At baseline immediately before the procedure and immediately after completion of the procedure, up to 120 minutes

Secondary outcomes (8)
  1. Number of Participants Requiring Access-Site Crossover During the Coronary Interventional Cardiology Procedure

    Access-site crossover is defined as the need to change from the initially selected arterial access site to another arterial access site during the coronary interventional cardiology procedure. The occurrence of crossover and the alternative arterial access site used will be recorded.

    Measured: During the coronary interventional cardiology procedure, up to 120 minutes

  2. Mean Procedural Pain Score Assessed by the Visual Analog Scale (VAS)

    Procedural pain will be assessed using the Visual Analog Scale (VAS), consisting of a 10-cm horizontal line ranging from 0 ("no pain") to 10 ("worst possible pain"). Immediately after the procedure, participants will indicate the overall level of pain experienced throughout the entire coronary interventional cardiology procedure. Higher scores indicate greater pain.

    Measured: immediately after the cardiology procedure, up to 120 minutes

  3. Mean Change From Baseline in Heart Rate

    Heart rate will be measured using a digital monitor and recorded in beats per minute. The outcome will be expressed as the mean change in heart rate from baseline to immediately after the coronary interventional cardiology procedure.

    Measured: At baseline immediately before the procedure and immediately after completion of the procedure, up to 120 minutes

  4. Number of Participants With Adverse Reactions

    Adverse reactions occurring in study participants will be recorded at the post-procedure assessment. The number of participants experiencing an adverse reaction and the type of reaction will be documented.

    Measured: Immediately after the cardiology procedure,up to 120 minutes

  5. Number of Participants Who Withdraw From the Study

    The number of participants who withdraw from the study will be recorded. The reason for withdrawal, when available, will also be documented.

    Measured: From enrollment through completion of the post-procedure assessment, up to 1 day

  6. Mean Change From Baseline in Peripheral Oxygen Saturation (SpO2)

    Peripheral oxygen saturation (SpO2) will be measured using a digital monitor and recorded as a percentage. The outcome will be expressed as the mean change in SpO2 from baseline to immediately after the coronary interventional cardiology procedure.

    Measured: At baseline immediately before the procedure and immediately after completion of the procedure, up to 120 minutes

  7. Mean Change From Baseline in Systolic Blood Pressure

    ystolic blood pressure will be measured using a digital monitor and recorded in millimeters of mercury (mmHg). The outcome will be expressed as the mean change in systolic blood pressure from baseline to immediately after the coronary interventional cardiology procedure.

    Measured: At baseline immediately before the procedure and immediately after completion of the procedure, up to 120 minutes

  8. Mean Change From Baseline in Diastolic Blood Pressure

    Diastolic blood pressure will be measured using a digital monitor and recorded in millimeters of mercury (mmHg). The outcome will be expressed as the mean change in diastolic blood pressure from baseline to immediately after the coronary interventional cardiology procedure.

    Measured: At baseline immediately before the procedure and immediately after completion of the procedure, up to 120 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Aug 2026
  2. Study start1 Sep 2026 (estimated)
  3. Primary completion31 Aug 2029 (estimated)
  4. Study completion31 Oct 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
208 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07786961
Sponsor's protocol ID
AOSassari_MM
Acronym
MUSICOR
Status last verified
Aug 2026
First submitted
20 Aug 2026
Last updated
26 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Spielberger, C. D., Gorsuch, R. L., Lushene, R., Vagg, P. R., & Jacobs, G. A. (1983). Manual for the State-Trait Anxiety Inventory (Form Y). Consulting Psychologists Press.

  • Pedrabissi, L., & Santinello, M. (1989). Inventario per l'ansia di "stato" e di "tratto": Nuova versione italiana dello STAI, forma Y: Manuale. Organizzazioni Speciali.

  • Kokalj Palandačić, A., Učman, S., Novak Šarotar, B., & Lainščak, M. (2023). The manifestation of anxiety in patients undergoing elective coronary angiography. European Psychiatry, 66(S1), S69. https://doi.org/10.1192/j.eurpsy.2023.233

  • Weeks BP, Nilsson U. Music interventions in patients during coronary angiographic procedures: a randomized controlled study of the effect on patients' anxiety and well-being. Eur J Cardiovasc Nurs. 2011 Jun;10(2):88-93. doi: 10.1016/j.ejcnurse.2010.07.002. Epub 2010 Aug 3.

    PubMed 20685168
  • Wang YR, Hung YY, Lu SF. Effect of music-based interventions on anxiety and stress-related vital signs in patients undergoing cardiac catheterization: A systematic review and meta-analysis. Complement Ther Med. 2024 Oct;85:103078. doi: 10.1016/j.ctim.2024.103078. Epub 2024 Aug 28.

    PubMed 39209008
  • Su SF, Yeh WT. Music Interventions in Percutaneous Coronary Procedures: A Meta-Analysis. Clin Nurs Res. 2021 Feb;30(2):135-145. doi: 10.1177/1054773819883171. Epub 2019 Oct 18.

    PubMed 31625397
  • Moon JR, Song J, Huh J, Kang IS, Kim JH, Park SW, Chang SA. The effects of music intervention on anxiety and stress responses in adults with CHD undergoing cardiac catheterisation. Cardiol Young. 2023 Feb;33(2):213-220. doi: 10.1017/S1047951122000439. Epub 2022 Mar 14.

    PubMed 35285439
  • Micheluzzi V, Burrai F, Casula M, Serra G, Al Omary S, Merella P, Casu G. Effectiveness of virtual reality on pain and anxiety in patients undergoing cardiac procedures: A systematic review and meta-analysis of randomized controlled trials. Curr Probl Cardiol. 2024 May;49(5):102532. doi: 10.1016/j.cpcardiol.2024.102532. Epub 2024 Mar 19.

    PubMed 38503359
  • Hawker GA, Mian S, Kendzerska T, French M. Measures of adult pain: Visual Analog Scale for Pain (VAS Pain), Numeric Rating Scale for Pain (NRS Pain), McGill Pain Questionnaire (MPQ), Short-Form McGill Pain Questionnaire (SF-MPQ), Chronic Pain Grade Scale (CPGS), Short Form-36 Bodily Pain Scale (SF-36 BPS), and Measure of Intermittent and Constant Osteoarthritis Pain (ICOAP). Arthritis Care Res (Hoboken). 2011 Nov;63 Suppl 11:S240-52. doi: 10.1002/acr.20543. No abstract available.

    PubMed 22588748
  • Bradt J, Dileo C, Potvin N. Music for stress and anxiety reduction in coronary heart disease patients. Cochrane Database Syst Rev. 2013 Dec 28;2013(12):CD006577. doi: 10.1002/14651858.CD006577.pub3.

    PubMed 24374731

Questions about this trial

What is this clinical trial studying?

A study testing Music Medicine intervention in people with Acute Coronary Syndrome, run by Azienda Ospedaliero Universitaria di Sassari at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 26 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Valentina Micheluzzi, PhD (+39 3401753630, valentina.micheluzzi@aousassari.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Mean Change From Baseline in State Anxiety Score Assessed by the State-Trait Anxiety Inventory (STAI-Y1) (time frame: At baseline immediately before the procedure and immediately after completion of the procedure, up to 120 minutes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07786961, which also lists 10 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Aug 2026.

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