Computer-Assisted Speech Training for Hearing Aid Users

Hearing Impairment Clinical Trial

Official title: Effect of Computer-Assisted Speech Training on Speech Recognition and Subjective Benefits for Hearing Aid Users With Severe to Profound Prelingual Hearing Loss

Status Completed

Clinical Trial Summary

Computer-assisted speech training is a speech recognition training system developed for cochlear implant users. With minimal facilities and skills, cochlear implant users can conduct this training at home. The purpose of this study was to apply this system to adolescent and young adult hearing aid users with prelingual severe to profound hearing loss.

Clinical Trial Description

Introduction Sensorineural hearing loss (SNHL) is a disability affecting people worldwide, and the prevalence is expected to increase due to prolonged life expectancy. SNHL has a significant negative impact on the quality of life, especially in prelingually deafened children. Except for certain diseases such as sudden deafness or endolymphatic hydrops, which may be treated or alleviated by medication or surgery, most patients with SNHL have to wear hearing aids or undergo cochlear implantation to regain hearing. However, for many individuals these measures do not satisfactorily resolve communication problems, because hearing is only the first step in a series of events leading to communication. Between hearing and communication lie the important skills of listening and comprehension, and to achieve successful communication it has been suggested that patients receiving amplification should be offered some type of audiological rehabilitation. It has been reported that older subjects do not spontaneously acclimatize to wearing a hearing aid, or that the effects are either small or nonexistent, which emphasizes the importance of rehabilitation after wearing a hearing aid. Unfortunately, not everyone with SNHL in Taiwan receives this kind of rehabilitation. The reasons for this may be: (a) methods of rehabilitation are not familiar to all clinicians or speech pathologists; (b) there is a shortage of clinicians or speech pathologists to provide such time-consuming rehabilitation; (c) hearing impaired patients may be unable to afford or are unwilling to dedicate time to rehabilitation; and (d) it is difficult to measure the improvements provided by rehabilitation.

Recently, rehabilitative training procedures have been garnering interest due to technological advances enabling a hearing aid user to perform the procedures while at home using a personal computer. Burk et al trained young normal-hearing and older hearing-impaired listeners with digitally recorded training materials using a computer. The results showed that older hearing-impaired listeners were able to significantly improve their word-recognition abilities through training with one talker, and to some degree achieve the same level as young normal-hearing listeners. In addition, the improved performance was maintained across talkers and across time.

The computer-aided speechreading training (CAST) system was developed to simulate a face-to-face training intervention and was designed to be one component of a comprehensive aural rehabilitation program for preretirement adults with acquired mild-to-moderate hearing loss. The aim of the training was to enhance speechreading skills to complement auditory speech perception. Throughout the training, the learner views a monitor that shows either a computer-generated screen or a videotaped recording of the teacher. CAST was designed to be used by a clinician to extend rather than to replace existing rehabilitative techniques.

Computer-based training has also been applied to the rehabilitation of cochlear implant users. Before the development of computer-based training, some studies assessed the effects of limited training on the speech-recognition skills of poorer-performing cochlear implant users. Busby et al conducted ten 1-hour speech perception and production training sessions, and the results demonstrated minimal changes in perceptual abilities in three cochlear implant users. Dawson and Clark conducted one 50-minute training session per week for 10 weeks, and four of five subjects showed some measure of improvement. The limited success of these attempts to improve the speech-recognition abilities of cochlear implant users was thought to be due to an inadequate amount of training. More intensive training of cochlear implant users was predicted to be effective, because in normal hearing populations training has been shown to successfully improve speech segment discrimination and identification, and recognition on spectrally shifted speech. Fu et al reported encouraging results in the rehabilitation of cochlear implant users using a computer-assisted speech training system which they also called CAST, although this was different to the CAST system of Pichora-Fuller and Benguerel. The CAST system of Fu et al, developed at the House Ear Institute, contains a large database of training materials and can be installed on personal computers, and so with minimal facilities and skills, cochlear implant users can conduct the training at home, and clinicians or speech pathologists can monitor the subject's test score and training progress. The results demonstrated that after moderate amounts of training (1 hour per day, 5 days per week), all 10 postlingually deafened adult cochlear implant users in the study had significant improvements in vowel and consonant-recognition scores. Wu et al applied the CAST system to 10 Mandarin-speaking children (three hearing aid users and seven cochlear implant users). After training for half an hour a day, 5 days a week, for a period of 10 weeks, the subjects showed significant improvements in vowel, consonant and Chinese tone performance. This improved performance was largely retained for 2 months after the training had been completed. Stacey and Summerfield also used computer-based auditory training to improve the perception of noise. The results confirmed that the training helped to overcome the effects of spectral distortions in speech, and the training materials were most effective when several talkers were included.

Based on these previous studies, cochlear implant users can improve their speech recognition ability after training with a CAST system. If this system is also effective for hearing aid users, and especially prelingually deafened patients, the CAST system will have a substantially positive impact, as there are many more hearing aid users than cochlear implant users.

The purpose of this study was to train prelingually deafened adolescents and young adults with CAST and measure the benefits objectively and subjectively. The objective benefits were measured using published speech recognition tests [13], and the subjective benefits were measured using client-oriented scale of improvement (COSI).

Materials and Methods Subjects Fifteen hearing aid users with prelingual severe to profound hearing loss participated in this study. Another six hearing aid users with a similar age and hearing average were included as the control group. The inclusion criteria for the study subjects and controls were: (1) age above 15 years; (2) wearing a hearing aid for at least for 2 years after hearing loss was diagnosed; (3) basic ability to operate a computer; (4) Mandarin Chinese speaker; and (5) motivation to undertake the training program. The exclusion criteria were: (1) aided hearing average worse than 70 dBHL; (2) unable to operate a computer. Before training with CAST, all participants received unaided and aided sound field audiometry. Table 1 shows the basic information of the 21 participants.

Client-oriented scale of improvement (COSI) We use a COSI questionnaire to evaluate subjective benefits. Before training with the CAST system, both the training and control groups were asked to identify up five specific situations in which they would like to cope better. At the end of the training, for each situation they were asked (A) how much better (or worse) they could now hear, and (B) how well they were now able to cope. For scaling purposes, the responses were assigned scores from 1 to 5, with 5 corresponding to "much better" and "almost always", 4 corresponding to "better" and "most of the time", 3 corresponding to "slightly better" and "half the time", 2 corresponding to "no difference" and "occasionally", and 1 corresponding to "worse" and "hardly ever", for questions A and B, respectively. Question A was defined as an "improvement", and question B was defined as "final ability". The total scores of the five situations were compared between the training and control groups.

Test materials and procedures The speech recognition test materials including monosyllabic words, disyllabic spondee words, vowels, consonants and Chinese tone recognition tests were recorded onto a CD-ROM at Melody Medical Instruments Corp. by a male and female speaker. The test materials were displayed on a laptop computer connected to a GSI 61TM clinical audiometer (Grason-Stadler, USA) at an output level of 70 dBHL. The testing procedure was performed in a double-walled, sound-treated room.

Monosyllabic Chinese word recognition test materials included four blocks of 25 Chinese words. For each speech recognition test, 50 words were selected resulting in a set of 50 tokens. After a monosyllabic Chinese word was displayed, the participants were asked to write down the word. Four different sets of open-set tests were generated for each speech recognition test. Disyllabic Chinese spondee-word recognition test materials included two blocks of Chinese spondee-words, each block containing 36 Chinese spondee-words. For each speech recognition test, one block was selected resulting in a set of 36 tokens. After a Chinese spondee-word was displayed, the participants were asked to write down the word. Four different sets of open-set test were generated via changing the order of the materials for each speech recognition test.

Vowel recognition test materials included 16 Chinese words. Vowel recognition was measured using a 4-alternative, forced-choice procedure in which Chinese characters were shown on the choice list. For each speech recognition test, the order of the words was changed. Thus, four different sets of closed-set tests were generated. Consonant recognition test materials included 21 Chinese words. Consonant recognition was measured using a 4-alternative, forced-choice procedure in which a Chinese character was shown on the choice list. For each speech recognition test, the order of the words was changed, and thus four different sets of closed-set tests were generated. Chinese tone recognition test materials included 50 Mandarin Chinese words. The participants were asked to write down the Chinese tone (tone: 1: flat; 2: rising; 3: falling-rising; 4: falling) after the Chinese word was displayed. For each speech recognition test, the order of the words was changed, and thus four different sets of open-set tests were generated.

Before training, both groups underwent a series of speech recognition tests as baseline data. The training group then started training whereas the control group did not receive any training. Every 4 weeks, the participants returned to the lab for another series of speech recognition tests using different test materials. Every participant had received a total of four speech recognition tests by the end of the study.

Training tools and procedures CAST software developed at the House Ear Institute and distributed by Melody Medical Instrument Corp. was used as the training tool. The training group was instructed to train at home following the program for at least 1 hour per day, 3 days a week, for 12 successive weeks. The control group did not receive any training and returned to the lab every 4 weeks for speech recognition tests. For each participant in the training group, a baseline speech recognition test was performed after the software had been installed into his or her personal computer. The results were analyzed by the software which then automatically generated a targeted training program. The software contained a large amount of information including pure tone, vowel recognition, consonant recognition, tone recognition, speaker recognition, environmental sounds, occasional words and occasional sentences. The subjects were asked to focus on pure tone, vowel recognition, consonant recognition and tone recognition training. The subjects started the training at a level generated by the computer software. There were usually five levels of difficulty in each training category, and each level consisted of several training sessions. For pure tone recognition training, the subjects were asked to choose the sound different to the others. Visual feedback was provided as to whether the response was correct or incorrect. After a training session had been completed, the score was calculated. If the score exceeded 80, the training proceeded to a higher level. If the score did not exceed 80, the training session was repeated until the score exceeded 80. At a higher level of training sessions, the differences between speech features in the response choices were reduced. For vowel recognition training, the subjects were asked to choose the vowel different to the others. After the subjects had progressed beyond the 3-alternative forced-choice discrimination task, they were trained to identify final vowels. Similar training procedures were used for consonant and tone recognition training.

Each subject in the training group was asked to register on the Melody Medical Instrument Corp. website, and his or her username and password were provided to us. Therefore, we were able to monitor the total time spent training, and the training time and score for each exercise. If the subjects did not reach the required amount of time and training sessions, we contacted their family and encouraged them to do more training.

Statistical methods All statistical analyses were performed with SAS software (Version 9.1.3, SAS Institute Inc., Cary, NC, U.S.A.) and R software (Version 2.7). Two-sided p values of 0.05 or less were considered to be statistically significant. Continuous data were expressed as mean ± standard deviation (SD) unless otherwise specified. Percentages were calculated for categorical variables. Two-sample t tests or Wilcoxon rank-sum tests were used to compare the means or medians of continuous data between two groups, whereas the chi-squared test or Fisher's exact test was used to analyze categorical proportions between two groups.

In addition to univariate analyses, the data of the five speech recognition tests were analyzed by fitting multiple marginal linear regression models using generalized estimating equations. If the first-order autocorrelation (i.e., AR(1)) structure fit the repeated measures data well, the model-based standard error estimates were used in the generalized estimating equations analysis; otherwise, the empirical standard error estimates were reported. In addition, the data of COSI were analyzed by fitting multiple linear regression models.

Basic model-fitting techniques for variable selection, goodness-of-fit assessment, and regression diagnostics were used in our regression analyses to ensure the quality of the results. In stepwise variable selection, all of the univariate significant and non-significant covariates were considered, and both the significance levels for entry and for stay were set to 0.15 or larger. The goodness-of-fit measure, the coefficient of determination (R2), was computed for all of the linear regression models, which is the square of the correlation between the observed response variable and the predicted value. It had a value between 0 and 1, with a larger value indicating a better fit of the multiple linear regression model to the observed continuous data. In addition, the variance inflation factor was examined to detect potential multicollinearity problems (defined as a value ≥ 10). ;

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Deafness
• Hearing Impairment
• Hearing Loss

• NCT number: NCT02092337
• Study type: Interventional
• Source: National Taiwan University Hospital
• Status: Completed
• Phase: N/A
• Start date: June 2007
• Completion date: March 2008