Comparing Self-Fitting Strategies for Over-the-Counter Hearing Aids: A Crossover Clinical Trial.

IF 6 1区 医学 Q1 OTORHINOLARYNGOLOGY
Megan Knoetze, Vinaya Manchaiah, Karina De Sousa, David R Moore, De Wet Swanepoel
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引用次数: 0

Abstract

Importance: Fewer than 20% of US adults with hearing loss use hearing aids due to barriers like high cost. Over-the-counter (OTC) hearing aids offer a potential solution, incorporating self-fitting strategies via smartphone apps. Self-fitting strategies have been validated for Food and Drug Administration (FDA)-approved OTC hearing aids compared with prescription-based approaches. However, no direct comparative analysis exists between in situ audiometry and self-adjustment strategies using self-fitting OTC (OTC-SF) hearing aids.

Objective: To compare self-adjustment and in situ audiometry self-fitting strategies in OTC-SF hearing aids for adults with mild to moderate hearing difficulties.

Design settings and participants: A crossover, within-participant pseudorandomized clinical trial was conducted between July and November 2023. Twenty-eight participants were pseudo-randomly assigned to 1 of the 2 self-fitting strategies, and they experienced both interventions for 4 consecutive weeks.

Interventions: The self-adjustment group manually adjusted settings, including overall gain and spectral tilt, using Lexie B2 hearing aids, while the in situ audiometry group used Lexie B2 Plus hearing aids (Lexie Hearing by hearX Group), with an automated fitting based on in situ tests conducted through the app.

Main outcomes and measures: The primary outcome was Abbreviated Profile of Hearing Aid Benefit (APHAB). Secondary outcomes were International Outcome Inventory for Hearing Aids (IOI-HA), speech-in-noise tests (DIN and QuickSIN), and real-ear measurements (REMs). Measures were completed at baseline and after the 4-week field trial using each strategy.

Results: Twenty-eight participants (mean [SD] age, 60.2 [12.0] years) were included; 14 men and 14 women. Self-adjustment and in situ audiometry strategies produced no clinically meaningful differences across various outcome measures, including overall APHAB benefit (Cohen d = 0.2; 95% CI, -0.2 to 0.6) and overall IOI-HA satisfaction (Rosenthal r = 0.0; 95% CI, -0.3 to 0.2). Self-adjustment users reported higher satisfaction (Rosenthal r = -0.4; 95% CI, -0.6 to -0.1) and longer daily use (Rosenthal r = -0.3; 95% CI, -0.5 to 0.0) compared with those using in situ audiometry. No clinically meaningful differences were observed in speech-in-noise benefit and real-ear measurements.

Conclusion and relevance: In this clinical trial of OTC-SF hearing aids, self-adjustment and in situ audiometry strategies resulted in similar outcomes. However, self-adjustment may produce higher satisfaction and longer daily use, highlighting the potential advantages of active user involvement in the fitting process. Further investigation is needed for long-term outcomes.

Trial registration: ClinicalTrials.gov Identifier: NCT05782153.

比较非处方助听器的自我验配策略:交叉临床试验。
重要性:由于高昂的费用等障碍,只有不到 20% 的美国成人听力损失患者使用助听器。非处方(OTC)助听器提供了一种潜在的解决方案,它通过智能手机应用程序采用了自我装配策略。经美国食品和药物管理局(FDA)批准的非处方助听器与处方助听器相比,自我验配策略已得到验证。然而,目前还没有对现场测听和使用自配 OTC(OTC-SF)助听器的自我调节策略进行直接比较分析:比较轻度至中度听力障碍成人使用 OTC-SF 助听器进行自我调整和原位测听的自我验配策略:在 2023 年 7 月至 11 月期间进行了一项交叉、参与者内伪随机临床试验。28 名参与者被伪随机分配到两种自我验配策略中的一种,并在连续 4 周内体验两种干预方法:自我调整组使用 Lexie B2 助听器手动调整设置,包括总体增益和频谱倾斜度,而原位测听组使用 Lexie B2 Plus 助听器(Lexie Hearing by hearX Group),根据通过应用程序进行的原位测试进行自动验配:主要结果和测量指标:主要结果是助听器效益简表(APHAB)。次要结果为国际助听器结果量表(IOI-HA)、噪声言语测试(DIN 和 QuickSIN)以及真耳测量(REMs)。在基线和使用每种策略进行为期 4 周的现场试验后完成测量:共有 28 名参与者(平均 [SD] 年龄为 60.2 [12.0] 岁),其中男性 14 人,女性 14 人。在各种结果测量中,自我调整和原位测听策略没有产生有临床意义的差异,包括 APHAB 的总体收益(Cohen d = 0.2;95% CI,-0.2 至 0.6)和 IOI-HA 的总体满意度(Rosenthal r = 0.0;95% CI,-0.3 至 0.2)。与使用原位测听的用户相比,自我调整用户的满意度更高(Rosenthal r = -0.4;95% CI,-0.6 至 -0.1),每日使用时间更长(Rosenthal r = -0.3;95% CI,-0.5 至 0.0)。在噪声言语效益和实耳测量方面没有观察到有临床意义的差异:在这项 OTC-SF 助听器临床试验中,自我调节和现场测听的结果相似。然而,自我调节的满意度更高,日常使用时间更长,这凸显了用户积极参与验配过程的潜在优势。对于长期效果还需要进一步调查:试验注册:ClinicalTrials.gov Identifier:试验注册:ClinicalTrials.gov Identifier:NCT05782153。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.10
自引率
5.10%
发文量
230
期刊介绍: JAMA Otolaryngology–Head & Neck Surgery is a globally recognized and peer-reviewed medical journal dedicated to providing up-to-date information on diseases affecting the head and neck. It originated in 1925 as Archives of Otolaryngology and currently serves as the official publication for the American Head and Neck Society. As part of the prestigious JAMA Network, a collection of reputable general medical and specialty publications, it ensures the highest standards of research and expertise. Physicians and scientists worldwide rely on JAMA Otolaryngology–Head & Neck Surgery for invaluable insights in this specialized field.
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