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Auditory Diagnostics and Error-based Treatment

Auditory Diagnostics and Error-based Treatment - AuDiET

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON51557
Enrollment
45
Registered
2022-03-29
Start date
2022-05-30
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

deafness hearing loss

Interventions

Two distinct interventions are planned for the lower performing CI users, one concerning adjustments to their CI fitting and one concerning personalized auditory training.

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: * Adult (over 18 years old at the time of inclusion) * Post-lingually deafened (the subject had a good mastery of spoken language before onset of deafness) * Native Dutch speaker * Implanted, either unilaterally or bilaterally, with a Cochlear Implant manufactured by Cochlear Ltd (i.e., a Nucleus ® implant). * Implanted with one of the following implants: CI422, CI512, CI522, CI532, CI24R, CI24RE. * Implanted for at least 12 months.

Exclusion criteria

Exclusion criteria: A potential subject for the CI user group who meets any of the following criteria will be excluded from participation in this study: * Known abnormally formed cochlea * Known pre-implantation ossification of the cochlea * Severe cognitive disorders affecting their ability to understand spoken language * Intense facial nerve stimulation * Unaddressed electrode tip foldover * More than 4 electrodes deactivated because of malfunction (open/short circuit) or lack of response * Additional illnesses or handicaps that could impact the ability to participate in the study, at the clinician*s discretion.

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the level of improvement of phoneme and word recognition score on the individual scale after the interventions.

Secondary

MeasureTime frame
The secondary endpoints are: 1. the results of the exploratory analyses performed on the correlation between the spectrotemporal assessment test and the subjects* error profile. 2. the results of the exploratory analyses performed on the differences between error patterns in phoneme and word recognition tests, both between and within subjects. 3. The results of the SUS/IMI questionnaires concerning the individualized training app

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Aug 9, 2026