跳至主要内容
临床试验/NCT04762043
NCT04762043Unknown不适用

EMG Voice Restoration

Altec Inc.2 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2021年2月12日最近更新:
适应症

试验速览

阶段
不适用
发起方
Altec Inc.
入组人数
28
试验地点
2
主要终点
Pitch Recognition Accuracy

研究概览

简要总结

This study will evaluate the ability of MyoVoice to replace natural speech. Referred to generally as an Augmentative and Alternative Communication (AAC) device, MyoVoice uses electrical signals recorded non-invasively from speech muscles (electromyographic, or EMG, signals) to restore communication for those with vocal impairments that resulted from surgical treatment of laryngeal and oropharyngeal cancers.

详细描述

Over 7.5 million people worldwide are unable to vocalize effectively. Among these individuals are cancer survivors who underwent oropharyngeal/laryngeal surgery and must rely on AAC systems such as text-to-speech applications or artificial voice prostheses as substitutes for their natural voice. Yet most of these devices struggle to convey the expressive attributes of speech (prosody), leading to poor comprehension and a lack of emotional content. The clinical trial will investigate the feasibility of MyoVoice-a novel AAC device that uses surface EMG signals to extract patterns for understanding vocabulary and expressive attributes from articulatory musculature during silently mouthed speech-to effectively restore conversational capabilities for individuals living with vocal impairments due to surgical treatment of laryngeal and oropharyngeal cancers. Patients who underwent a total laryngectomy will be asked to communicate with a conversational partner by silently mouthing words using MyoVoice. The device performance will be evaluated in terms of its ability to accurately and quickly translate articulatory muscle activity into audible speech. MyoVoice will also be compared to that of conventional electrolaryngeal speech aids (i.e., artificial larynx) to evaluate device ease-of-use, functional efficacy, and social reception.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
25 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Control Subjects:
  • Primary English speaker
  • No history of speech, language, cognitive, or hearing disorders
  • Normal hearing (able to pass a bilateral hearing screening using a threshold of 25 dB HL at 125, 250, 500, 1000, 2000, 4000, and 8000 Hz based on the American Speech-Language-Hearing Association)
  • Capable of signed informed consent
  • Laryngectomy Subjects:
  • At least 6 months S/P total laryngectomy
  • Proficient electrolarynx (EL) speaker
  • Primary English speaker
  • Sufficiently available and sufficiently healthy to comply with multiple test sessions lasting 4-6 hours
  • Capable of signed informed consent

排除标准

  • Control Subjects:
  • Inability to understand spoken English or follow simple instructions
  • History of speech, language, cognitive, or hearing disorders
  • Inability to provide written informed consent
  • Laryngectomy Subjects:
  • Inability to understand spoken English or follow simple instructions
  • Loss of adequate sEMG sensor sites for recording from muscles of articulation due to Cancer treatment
  • Skin disorders or radiation/surgical scarring that prevent the use of medical-grade adhesive tapes for securing sensors
  • Inability to provide written informed consent
  • Any other medical or psychological condition that is based on the opinion of the investigators will prevent participation in the experiment (e.g., the candidate may have an illness that makes them fatigue easily or have difficulty to attend to visual cues)

结局指标

主要结局

Pitch Recognition Accuracy

时间窗: 30 mins to 2 hours

Percent accuracy between recognized (sEMG) and ground-truth (acoustic) estimates of fundamental frequency (perceptually known as vocal pitch). Accuracy is estimated on a continuous scale from 0 to 100%.

Loudness Recognition Accuracy

时间窗: 30 mins to 2 hours

Percent accuracy between recognized (sEMG) and ground-truth (acoustic) estimates of intensity level (perceptually related to vocal loudness). Accuracy is estimated on a continuous scale from 0 to 100%.

Speech Naturalness

时间窗: 30 mins to 1 hour

Percent naturalness between MyoVoice and electrolarynx speech samples. Speech naturalness is defined based on one's "preference for how \[the audio\] sounds in terms of rate, rhythm, intonation and voice quality." Naturalness is estimated on a continuous scale from 0 to 100%.

次要结局

未报告次要终点

研究者

发起方
Altec Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验