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Perioperative AnxietyNCT07206186

Effect of Music on Patient Comfort

A study testing Music in people with Perioperative Anxiety, run by Medical University of Vienna at 1 site in Austria.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

Perioperative anxiety remains a prevalent and significant concern for patients undergoing surgery, with substantial impacts on postoperative pain perception, patient satisfaction and recovery. Historically, anxiolytics (e.g. Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Perioperative Anxiety
What is being tested?
Music
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteAustria
Study dates
5 Jun 2025to 1 Sep 2026
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 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Written informed consent
  • Elective ophthalmological surgery under general anesthesia (e.g. strabismus surgery, cataract surgery or other lens surgery, glaucoma surgery, keratoplasty or other corneal transplantation, vitrectomy or other retinal surgery, lacrimal duct surgery)
  • Age: 18-70 years
  • ASA score I-II (American Society of Anesthesiologists)

Who cannot join

  • Pre-existing psychiatric disorder (e.g. anxiety disorder, PTSD, depression)
  • Chronic pain patients
  • Language barrier
  • Anticipated difficult airway
  • Pregnancy

Trial locations and contacts

1 site in 1 country.

Austria1 site
  • Medical University of Vienna

    Vienna, State of Vienna, 1090

Other trials in Austria

About this study

Official title: Music Listening During Anesthesia Induction and Emergence: Assessing Its Role in Enhancing Patient Comfort

Perioperative anxiety remains a prevalent and significant concern for patients undergoing surgery, with substantial impacts on postoperative pain perception, patient satisfaction and recovery. Historically, anxiolytics (e.g. benzodiazepines) were often routinely administered preoperatively in this context, accepting the potential negative side effects of pharmacotherapy. In recent literature, there is an increasing focus on alternative, non-pharmacological methods for anxiety reduction, such as music, music therapy, virtual reality, and hypnosis.

Music can represent an effective and cost-efficient option to reduce perioperative anxiety and stress. Most randomized controlled trials on this topic (music group vs. non-music group) have been conducted in pediatric patient populations, often showing significant results (i.e. significantly less anxiety in the music group, measured using standardized scales or inventories). In adult patient populations, considerably fewer randomized controlled trials with music interventions for perioperative anxiety reduction have been conducted so far.

Read more

This study aims to evaluate the role of music during anesthesia induction and emergence for perioperative anxiety reduction in a randomized controlled trial. Patients will be randomized preoperatively into either the intervention group (50 patients, music) or the control group (50 patients, no music), and a baseline level of preoperative anxiety will be assessed using the State-Trait Anxiety Inventory (STAI). In the intervention group, music of the patient's choice will be played starting from their arrival in the operating room during anesthesia induction, and again after the end of surgery during emergence from anesthesia. Afterwards, the effects of the music intervention on the patients' subjective well-being will be assessed in the intervention group postoperatively before discharge from the recovery room using four specific questions. In both groups, the State Anxiety Inventory (SAI) portion of the STAI will also be administered and the results compared.

In addition, the NASA Task Load Index will be administered to the attending anesthesiologists in both groups to evaluate whether the subjective workload of the anesthesiologists changes as a result of the music intervention.

Being tested
Music
Keywords
Perioperative Anxiety, Music, Music intervention, State Trait Anxiety Inventory (STAI), NASA Task Load Index, Anesthesia, Patient Comfort

What participants receive

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

  • MusicOther

    Music as per patient choice

Study groups in NCT07206186
Study groupRoleWhat they receive
Music groupExperimentalAfter randomization, the intervention group will be asked which type of music they would like to listen to during anesthesia induction and emergence. Upon arrival in the operating room, the selected music will be played from a wireless speaker at approximately 50-60 dB. The volume will be continuously monitored using a sound level meter and adjusted as needed. The music will stop once the airway is secured by the attending anesthetist (i.e. following endotracheal intubation or placement of a laryngeal mask). Music will resume after the surgery is completed, the bandage (if required) has been applied, and the administration of anesthetic medication has ceased. Music will be paused again after anesthesia emergence as the patient leaves the operating room.
Receives: Other: Music
Control groupNo interventionThe control group will not receive music during anesthesia induction or emergence. However, the State Trait Anxiety Inventory (STAI) will be administered preoperatively as well as the State Anxiety Inventory (SAI) portion of the STAI postoperatively.

What is being measured

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

  1. Impact of listening to self-selected music during anesthesia induction and emergence on patient well-being

    The primary objective of this randomized controlled trial is to assess the impact of listening to self-selected music during anesthesia induction and emergence on patient well-being, as measured by four specific questions:

    1. I enjoyed listening to the music I chose, during the anesthesia induction and emergence.
    2. Listening to the music I chose, during anesthesia induction and emergence had an anxiety relieving effect.
    3. Listening to the music I chose, during anesthesia induction and emergence had a stress-relieving effect.
    4. The next time I have a general anesthesia, I would like to listen to self-selected music during anesthesia induction and emergence.

    These questions will be answered using a Likert scale (strongly disagree - disagreee - neither agree nor disagree - agree - strongly agree).

    Measured: Postoperatively before discharge from the post-anesthesia care unit (PACU)

Secondary outcomes (6)
  1. Sex-specific differences regarding the primary objective

    Measured: Postoperatively before discharge from the post-anesthesia care unit (PACU)

  2. State Trait Anxiety Inventory (STAI)

    State Anxiety Inventory (SAI): pre- and postoperatively Trait Anxiety Inventory (TAI): preoperatively

    Measured: Pre- and postoperatively

  3. NASA Task Load Index (attending anesthesiologist)

    The NASA Task Load Index will be completed twice by the attending anesthesiologist in the presence of the study team: once after anesthesia induction, once patient stability and adequate anesthesia are confirmed, and again after anesthesia delivery, once the patient is stable in the post-anesthesia care unit (PACU) and all relevant information has been relayed to the PACU team.

    Measured: After anesthesia induction + after handover to the post-anesthesia care unit (PACU) team

  4. Attempts at airway management

    Intubation attempts Attempts to place a laryngeal mask

    Measured: After anesthesia induction

  5. Adverse events

    Including but not limited to:

    Difficult intubation > 3 attempts Respiratory complications (e.g. bronchospasm, laryngospasm) Hemodynamic complications (severe hypotension (MAP >50 for more than 5 minutes), severe bradycardia (heart rate < 40)) Cardiac arrest

    Measured: During surgery

  6. Postoperative pain in the post-anesthesia care unit (PACU)

    Opioid equivalents Non-opioid analgetic medication

    Measured: During the stay in the post-anesthesia care unit (PACU)

Timeline

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

  1. First posted3 Oct 2025
  2. Study start5 Jun 2025
  3. Primary completion9 Apr 2026
  4. Study completion1 Sep 2026 (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
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07206186
Sponsor's protocol ID
1166/2025
Status last verified
Jul 2026
First submitted
25 Sep 2025
Last updated
20 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Music in people with Perioperative Anxiety, run by Medical University of Vienna at 1 site in Austria.

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 4 inclusion and 5 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: under way, not looking for participants, as of the sponsor's last update on 20 Jul 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 Austria. 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?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Impact of listening to self-selected music during anesthesia induction and emergence on patient well-being (time frame: Postoperatively before discharge from the post-anesthesia care unit (PACU)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 20 Jul 2026.

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