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人耳听不到的 20 千赫兹超声对人体的影响。第二部分:双盲随机激发试验研究

Effects of very high-frequency sound and ultrasound on humans. Part II: A double-blind randomized provocation study of inaudible 20-kHz ultrasound.

机构信息

Faculty of Engineering and Physical Sciences, University of Southampton, University Road, Southampton SO17 1BJ, United Kingdom.

Department of Audiology and Hearing Therapy, Royal South Hants Hospital, Brinton's Terrace, Southampton SO14 0YG, United Kingdom.

出版信息

J Acoust Soc Am. 2018 Oct;144(4):2521. doi: 10.1121/1.5063818.

Abstract

Some people have reported symptoms such as nausea, dizziness, and headaches that they attribute to ultrasound (US) emitted by devices in public places. The primary aim of the present study was to investigate whether inaudible US can provoke adverse symptoms compared to a sham presentation, under double-blind conditions. A second aim was to investigate whether the expectation of US being present could provoke adverse symptoms (a nocebo response). The US stimulus was a 20 kHz tone presented continuously for 20 min set to at least 15 dB below the participants' detection threshold, giving a typical sound pressure level (SPL) of 84 dB. No evidence that US provoked symptoms was found, but there was evidence of small nocebo effects. A case study on an individual with high self-reported sensitivity to US gave similar results. The present study did not reproduce the severe symptoms reported previously by some members of the public; this may be due to the SPL or duration of the stimulus, or strength of the nocebo stimulus. These findings cannot be used to predict outcomes from exposures to sounds that are audible to the individual in question, or to sounds with higher SPLs, longer durations, or different frequency content.

摘要

一些人报告了一些症状,如恶心、头晕和头痛,他们将这些症状归因于公共场所设备发出的超声波(US)。本研究的主要目的是在双盲条件下,调查不可听的 US 是否会引起与假刺激相比的不良症状。第二个目的是调查对 US 存在的期望是否会引起不良症状(反安慰剂反应)。US 刺激是一种 20 kHz 的音调,连续播放 20 分钟,设置为至少低于参与者检测阈值 15 dB,典型的声压级(SPL)为 84 dB。没有证据表明 US 引起了症状,但有证据表明存在轻微的反安慰剂效应。对一个自我报告对 US 高度敏感的个体的案例研究得出了类似的结果。本研究没有复制先前一些公众报告的严重症状;这可能是由于刺激的 SPL 或持续时间,或反安慰剂刺激的强度。这些发现不能用于预测个体可听到的声音暴露或 SPL 更高、持续时间更长或频率内容不同的声音的结果。

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