ClinicalTrials.gg
Not yet recruitingNCT07786961MUSICORUpdated Aug 26, 2026

Music Medicine in Coronary Interventional Cardiology Procedures

An interventional study of Music Medicine intervention in Acute Coronary Syndrome, sponsored by Azienda Ospedaliero Universitaria di Sassari. Not yet recruiting at 1 site in Italy. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-08-26.

Sponsored by Azienda Ospedaliero Universitaria di Sassari · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
208
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study 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. 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.

02

Conditions studied

  • Acute Coronary Syndrome

Keywords

  • Music Medicine
  • Acute Coronary Syndrome
  • Percutaneous Coronary Intervention
  • Coronary Angiography
03

In context

Acute Coronary Syndrome

1,488 studies on the registry are indexed under Acute Coronary Syndrome; 273 are open to participants now.

This study's planned enrollment of 208 is close to the median of 200 across 865 interventional studies indexed under Acute Coronary Syndrome.

Browse Acute Coronary Syndrome studies →

Lead sponsor

Azienda Ospedaliero Universitaria di Sassari is the lead sponsor of 8 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

Exclusion criteria

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.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
208 participants (estimated)

Study arms

  • Experimental
    Music Medicine arm

    Patients 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

    Other: Music Medicine intervention

  • No intervention
    Standard Care Arm

    Patients 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.

Interventions

  • OtherMusic Medicine intervention

    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.

    Also known as: Music Therapy

06

What researchers measure

Primary outcomes

  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.

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

Secondary outcomes

  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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

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

07

Study locations

1 site
08

References and documents

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 ↗

Individual participant data

Plan to share: Undecided

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Sep 2026; primary completion for Aug 2029, 35 months later.

Of 210 non-industry interventional studies with no phase under Acute Coronary Syndrome, half reached primary completion within 34 months of starting (the median), counting those still running; a quarter within 17 and three quarters within 46. This study's planned 35 months is close to that.

Counting every sponsor, half of 225 studies reached it within 34 months; a quarter within 18 and three quarters within 46.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 20, 2026
First posted
Aug 26, 2026
StartEst.
Sep 1, 2026
Primary completionEst.
Aug 31, 2029
CompletionEst.
Oct 31, 2029
Last update
Aug 26, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 26, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07786961
Lead sponsor
Azienda Ospedaliero Universitaria di Sassari
Responsible party
Valentina Micheluzzi (Principal Investigator, Azienda Ospedaliero Universitaria di Sassari) — Principal investigator
First posted
Aug 26, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Aug 31, 2029 (estimated)
Completion
Oct 31, 2029 (estimated)
Last update
Aug 26, 2026

Study contacts

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

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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