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Enrolling by invitation NCT07639788

The Impact of Classical Music on Performance in Robotic Surgery Simulation

No phase Interventional Surgical Surgical Behaviour in the Operating Room Da Vinci Robot da Vinci SP Surgical System

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Exposure to Classical Music.
Who it may be relevant to
Registry conditions: Surgical, Surgical Behaviour in the Operating Room, Da Vinci Robot, da Vinci SP Surgical System. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Austria
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

In this experimental crossover study using the da Vinci simulator, the aim is to investigate how classical music influences the surgical performance of medical students. Following a brief training phase, participants complete standardized tasks under two conditions (no music vs. classical music). Performance is assessed using an objective trainer score. The study is conducted in a risk-free simulation environment, the stimuli are standardized, participation is voluntary, and data are collected in a pseudonymized manner. The goal is to obtain evidence-based insights into the effects of music and distraction on training and the working environment in robotic surgery.

Interventions

  • Behavioral Exposure to Classical Music
    Exposure to Classical Music through headphones while performing standardized exercises on the da Vinci robotic surgery simulator.

Primary outcome measures

  • Da Vinci Surgical Performance Score [Time frame: Once after each cycle (estimated: 15 minutes per cycle) of performing the standardized simulated surgical tasks (once with and once without exposure to Classical Music), the Performance Score will be measured by the simulation system.]
Secondary outcome measures (2)
  • Subjective Performance Score 1 [Time frame: After each cycle (estimated: 15 minutes per cycle)of performing the standardized simulated surgical tasks (once with and once without exposure to Classical Music), the Subjective Performance Score will be measured by the SURG-TLX.]
  • Subjective Performance Score 2 [Time frame: After each cycle (estimated: 15 minutes per cycle) of performing the standardized simulated surgical tasks (once with and once without exposure to Classical Music), the Subjective Performance Score will be measured by the additional questionnaire.]

Eligibility criteria

Inclusion criteria

The study includes adult (≥ 18 years) medical students between the first completed and the twelfth completed semester. Prior experience in robotic surgery or with training simulators is not required; however, basic familiarity with the use of technical devices is necessary. Furthermore, participants must have sufficient knowledge of German or English to provide informed consent and fully understand the instructions.

Exclusion criteria

  • Lack of capacity to provide informed consent
  • Insufficient language proficiency (German/English)
  • Known hypersensitivity to noise
  • Hearing or balance disorders
  • Conditions that significantly affect attention or motor skills (e.g., tremor, myopathies)
  • Acute illnesses that may impair participation, substance influence, or severe fatigue
  • Direct dependency or evaluative relationship with members of the study team

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Crossover
Masking
Single blind
Primary purpose
Basic science

Study locations

Austria · 1 center
  • Medical University of Vienna — Vienna

Identifiers

NCT: NCT07639788 · 1041/2026

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗