Use of Electropalatography to Improve Speech Sound Production
Hearing Impairment
About this trial
This is an interventional treatment trial for Hearing Impairment
Eligibility Criteria
Inclusion Criteria:
- All participants in this study will be at least 3 years post-implant and they must use the implants consistently.
- Participants who have adventitious/acquired hearing loss must have had normal hearing through their 18th year.
- Participants with congenital hearing loss will have received oral or total communication education, worn hearing aids and consider themselves to be "oral deaf" adults.
Exclusion Criteria:
- Individuals who do not meet this criteria will be excluded from the protocol.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Congenitally deaf
Adventitiously deaf
Prior and post speech training, participants will read aloud a standard paragraph (Rainbow passage), complete a traditional speech test (Goldman Fristoe Test of Articulation - 3) to assess the sounds of the English language in all word positions (initial, medial, final) and read a list of consonant-vowel-consonant (CVC) combinations. Individual treatment will be provided once a week for 10 consecutive weeks. Traditional speech intervention with visual biofeedback from the EPG will be used. Auditory feedback will be provided through the participants own cochlear implant.
Prior and post speech training, participants will read aloud a standard paragraph (Rainbow passage), complete a traditional speech test (Goldman Fristoe Test of Articulation - 3) to assess the sounds of the English language in all word positions (initial, medial, final) and read a list of CVC combinations. Individual treatment will be provided once a week for 10 consecutive weeks. Traditional speech intervention with visual biofeedback from the EPG will be used. Auditory feedback will be provided through the participants own cochlear implant.