Masalski Marcin, Grysiński Tomasz, Kręcicki Tomasz
Department and Clinic of Otolaryngology, Head and Neck Surgery, Faculty of Postgraduate Medical Training, Wroclaw Medical University, Wrocław, Poland.
Department of Biomedical Engineering, Faculty of Fundamental Problems of Technology, Wroclaw University of Science and Technology, Wrocław, Poland.
JMIR Mhealth Uhealth. 2018 Jan 10;6(1):e10. doi: 10.2196/mhealth.7800.
Hearing screening tests based on pure-tone audiometry may be conducted on mobile devices, provided that the devices are specially calibrated for the purpose. Calibration consists of determining the reference sound level and can be performed in relation to the hearing threshold of normal-hearing persons. In the case of devices provided by the manufacturer, together with bundled headphones, the reference sound level can be calculated once for all devices of the same model.
This study aimed to compare the hearing threshold measured by a mobile device that was calibrated using a model-specific, biologically determined reference sound level with the hearing threshold obtained in pure-tone audiometry.
Trial participants were recruited offline using face-to-face prompting from among Otolaryngology Clinic patients, who own Android-based mobile devices with bundled headphones. The hearing threshold was obtained on a mobile device by means of an open access app, Hearing Test, with incorporated model-specific reference sound levels. These reference sound levels were previously determined in uncontrolled conditions in relation to the hearing threshold of normal-hearing persons. An audiologist-assisted self-measurement was conducted by the participants in a sound booth, and it involved determining the lowest audible sound generated by the device within the frequency range of 250 Hz to 8 kHz. The results were compared with pure-tone audiometry.
A total of 70 subjects, 34 men and 36 women, aged 18-71 years (mean 36, standard deviation [SD] 11) participated in the trial. The hearing threshold obtained on mobile devices was significantly different from the one determined by pure-tone audiometry with a mean difference of 2.6 dB (95% CI 2.0-3.1) and SD of 8.3 dB (95% CI 7.9-8.7). The number of differences not greater than 10 dB reached 89% (95% CI 88-91), whereas the mean absolute difference was obtained at 6.5 dB (95% CI 6.2-6.9). Sensitivity and specificity for a mobile-based screening method were calculated at 98% (95% CI 93-100.0) and 79% (95% CI 71-87), respectively.
The method of hearing self-test carried out on mobile devices with bundled headphones demonstrates high compatibility with pure-tone audiometry, which confirms its potential application in hearing monitoring, screening tests, or epidemiological examinations on a large scale.
基于纯音听力测定的听力筛查测试可以在移动设备上进行,前提是这些设备经过专门校准。校准包括确定参考声级,并且可以相对于听力正常者的听力阈值进行。对于制造商提供的设备以及捆绑的耳机,参考声级可以针对同一型号的所有设备一次性计算出来。
本研究旨在比较使用特定型号、生物学确定的参考声级校准的移动设备测量的听力阈值与纯音听力测定获得的听力阈值。
通过在耳鼻喉科诊所患者中进行面对面提示,线下招募试验参与者,这些患者拥有配备捆绑耳机的安卓移动设备。通过一个开放获取的应用程序“听力测试”在移动设备上获得听力阈值,该应用程序包含特定型号的参考声级。这些参考声级先前是在与听力正常者的听力阈值相关的未控制条件下确定的。参与者在隔音室中在听力学家的协助下进行自我测量,测量内容包括确定设备在250Hz至8kHz频率范围内产生的最低可听声音。将结果与纯音听力测定进行比较。
共有70名受试者参与试验,其中男性34名,女性36名,年龄在18 - 71岁之间(平均36岁,标准差[SD]11)。移动设备上获得的听力阈值与纯音听力测定确定的阈值有显著差异,平均差异为2.6dB(95%CI 2.0 - 3.1),标准差为8.3dB(95%CI 7.9 - 8.7)。差异不大于10dB的数量达到89%(95%CI 88 - 91),而平均绝对差异为6.5dB(95%CI 6.2 - 6.9)。基于移动设备的筛查方法的敏感性和特异性分别计算为98%(95%CI 93 - 100.0)和79%(95%CI 71 - 87)。
在配备捆绑耳机的移动设备上进行听力自我测试的方法与纯音听力测定具有高度兼容性,这证实了其在听力监测、筛查测试或大规模流行病学检查中的潜在应用。