About this trial
Noise in hospital environments, particularly in operating rooms, poses challenges to both patient comfort and healthcare professionals' performance. Among the sources of noise, anesthesia monitoring alarms are essential for patient safety, yet no clear guidelines exist regarding their optimal sound level. Excessive alarm volume may increase distraction and cognitive load, especially for surgical trainees, potentially impairing their focus and performance during procedures. This randomized pilot interventional study aims to evaluate the impact of anesthesia alarm sound intensity on the mental workload of surgical trainees performing simulated surgeries. Participants will be randomly assigned to conditions with either an optimized alarm volume or a higher standard volume during simulated tasks. Cognitive load will be assessed using objective physiological measures such as heart rate variability and pupillometry, as well as subjective evaluations with tools like the NASA-TLX and SURG-TLX scales. The primary goal is to determine whether an optimized alarm sound level can reduce cognitive strain without compromising vigilance required for patient safety. Findings from this study are expected to provide evidence-based recommendations for auditory ergonomics in operating rooms, ultimately improving working conditions for surgical teams and enhancing both training and patient safety.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Surgical residents or experienced surgeons;
Surgeons with normal hearing;
Surgeons capable of performing surgical sutures (regardless of skill level);
Surgeons able and willing to follow all study procedures according to the protocol;
Disqualifiers
Surgeons undergoing beta-blocker treatment;
Surgeons with known cardiac pathology;
Surgeons who do not consent to participate in the study;
Surgeons with known hearing problems;
Trial design
Single group
Treatments tested in this trial
effects of sound
Other interventionThe surgical trainees will perform four 15-minute surgical sequences in a controlled environment, with varying sound levels (64, 67, 73, and 75 dB(A)) randomized across the sequences to assess the surgeons' responses.
Treatment groups
Trial outcomes
Primary outcomes
Impact of the optimal sound intensity level during a surgical procedure
Assessment of heart and respiratory rate variability parameters
Secondary outcomes
Interference with the surgical procedure
Measurement using the SURG-TLX (Surgical Task Load Index) questionnaire
Mental workload of the surgical trainee
Measurement using the SURG-TLX scale.
Locations
Sponsors and contacts
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