Maryn Youri, Dedry Marie, de Mahieu Valentine, Fournier-Foch Julie
European Institute for ORL-HNS, Department of Otorhinolaryngology and Head & Neck Surgery, Sint-Augustinus GZA, Wilrijk, Antwerp, Belgium; Department of Rehabilitation Sciences, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium; School of Logopedics, Faculty of Psychological and Educational Sciences, Université Catholique de Louvain, Louvain-La-Neuve, Belgium; Department of Speech-Language Pathology and Audiology, University College Ghent, Ghent, Belgium; Phonanium, Lokeren, Belgium.
School of Logopedics, Faculty of Psychological and Educational Sciences, Université Catholique de Louvain, Louvain-La-Neuve, Belgium; Psychological Sciences Research Institute, Université Catholique de Louvain, Louvain-la-Neuve, Belgium; Institute of Neuroscience, Université Catholique de Louvain, Brussels, Belgium.
J Voice. 2024 Sep 7. doi: 10.1016/j.jvoice.2024.08.023.
OBJECTIVES/HYPOTHESIS: To develop sham voice treatment techniques to be used in voice treatment outcome research, and to investigate their effectiveness as sham. This entails that the techniques induce no changes in voice or voice physiology, yet still lead to a perception of efficacy.
Prospective randomized blinded controlled study.
Three distinct sham intervention protocols (SIPs) were conceptualized as placebic comparators for three common voice treatment approaches with focus on vocalization (SIP1), respiration (SIP2), and manipulation (SIP3). Forty-eight female students participated in the study. Each participant attended ten 30-minute sessions over 5weeks, including a baseline evaluation, three sessions of one SIP, an inter-SIP voice assessment, three sessions of a second SIP, and a final post-SIP assessment. Auditory-perceptual and instrumental voice evaluations were used as voice treatment outcome measures. The participants' perception of voice-related quality of life was evaluated using the French Voice Handicap Index (VHI). Frequentist as well as Bayesian statistical methods were applied for group comparisons. The effects of combining two SIPs, the potential influence of SIP order, and experimenter/clinician effects, were also investigated.
The respiration-based SIP2 showed changes only in sound intensity level on a sustained vowel across the three sham intervention sessions. In contrast, the vocalization-based SIP1 impacted sound intensity level on a sustained vowel, sound intensity level on read text, and maximum phonation time. The manipulation-based SIP3 affected smoothed cepstral peak prominence on read text, Acoustic Voice Quality Index, and Dysphonia Severity Index. SIP2 thus demonstrated the highest alignment with the study's objectives, followed by SIP1 and SIP3. GRBASI ratings revealed no statistical differences for any SIP. VHI decreased significantly after all three SIPs. Combining the SIPs generally replicated the effects observed when each SIP was used individually. There was no order effect or experimenter/clinician effect on the results.
This study demonstrated significant changes in participants' perceived voice quality (measured with VHIFr) across various SIPs, despite minimal impact on objective voice function measures. Further investigation is necessary to establish one or more protocols as genuinely sham interventions.
目的/假设:开发用于嗓音治疗效果研究的假嗓音治疗技术,并研究其作为安慰剂的有效性。这意味着这些技术不会引起嗓音或嗓音生理学的变化,但仍会导致疗效的感知。
前瞻性随机双盲对照研究。
三种不同的假干预方案(SIPs)被概念化为三种常见嗓音治疗方法的安慰剂对照,重点分别为发声(SIP1)、呼吸(SIP2)和手法操作(SIP3)。48名女学生参与了该研究。每位参与者在5周内参加10次30分钟的课程,包括一次基线评估、三种SIP之一的三次课程、SIP间嗓音评估、第二种SIP的三次课程以及最终的SIP后评估。听觉感知和仪器嗓音评估用作嗓音治疗效果指标。使用法语嗓音障碍指数(VHI)评估参与者对嗓音相关生活质量的感知。采用频率学派和贝叶斯统计方法进行组间比较。还研究了两种SIP联合使用的效果、SIP顺序的潜在影响以及实验者/临床医生的影响。
基于呼吸的SIP2在三个假干预课程中仅在持续元音的声强水平上显示出变化。相比之下,基于发声的SIP1影响持续元音的声强水平、朗读文本的声强水平以及最大发声时间。基于手法操作的SIP3影响朗读文本的平滑谐波峰值突出度、声学嗓音质量指数和嗓音障碍严重程度指数。因此,SIP2与研究目标的一致性最高,其次是SIP1和SIP3。GRBASI评分显示任何SIP均无统计学差异。所有三种SIP后VHI均显著下降。联合使用SIP通常会重现单独使用每种SIP时观察到的效果。结果不存在顺序效应或实验者/临床医生效应。
本研究表明,尽管对客观嗓音功能指标影响极小,但在各种SIP中,参与者感知的嗓音质量(用VHIFr测量)有显著变化。需要进一步研究以确定一种或多种方案作为真正的假干预措施。