Bilateral Hearing Loss, Sensorineural Hearing Loss, Bilateral
Conditions
Keywords
Cochlear implant, Bimodal fitting, Anatomy-based fitting
Brief summary
Main objective: For a bimodal fitting (hearing aid (HA) + cochlear implant (CI)): Comparison of a tonotopy based fitting strategy (TFS4) to a default fitting strategy (FS4) for the speech recognition in noise. Secondary objectives: Comparison of TFS4 to FS4 for speech recognition in quiet. Comparison of TFS4 to FS4 for the auditory skills experienced by the subject.
Detailed description
Introduction: Cochlear implantation allows the rehabilitation of profound bilateral deafness, restoring speech perception and verbal communication when the traditional hearing aid no longer provides satisfactory hearing gain. A cochlear implant includes an electrode array and its functioning is based on the principle of cochlear tonotopy: Each electrode encodes a frequency spectrum according to its position in the cochlea (high frequencies are assigned to the basal electrodes and low frequencies to the apical electrodes). The cochlear implant thus breaks down the frequency spectrum into a number of frequency bands via bandpass filters corresponding to the number of electrodes in the implant. During the fitting these bands can be modified by the audiologist. Bimodal hearing refers to the use of a CI in one ear with a HA on the contralateral side. This association allows for adults and children a better perception of speech in quiet and in noise, a better perception of music, hearing comfort, better sound quality, better localization of sound and, consequently, a better quality of life compared to unilateral CI alone. However, there is great variability in the integration process; while some bimodal users show substantial benefits, others receive little or no benefit. This variability could be due to the mismatch of frequencies (tonotopic shift) between the CI and the contralateral HA. Recently MED-EL has developed an "anatomy-based fitting" (ABF) strategy based on the tonotopy that allows, from a postoperative scanner, to calculate the theoretical characteristic frequency of neurons stimulated by each electrode contact and to transmit this information to the fitting software of the CI. This strategy (TFS4) could therefore allow a better integration of information in bimodal hearing and in particular improve the speech recognition in noise compared to a default strategy (FS4). Main objective: For a bimodal fitting (hearing aid (HA) + cochlear implant (CI)): Comparison of a tonotopy based fitting strategy (TFS4) to a default fitting strategy (FS4) for the speech recognition in noise. Secondary objectives: Comparison of TFS4 to FS4 for speech recognition in quiet. Comparison of TFS4 to FS4 for the auditory skills experienced by the subject. Plan of the study: It is a prospective open monocentric randomized crossover study: Measures will be done on the patient at 6 weeks and 12 weeks post-activation.
Interventions
DEVICEFS4 then TFS4 (cochlear implant)
Cochlear implant with default fitting then with tonotopy-based fitting
DEVICETFS4 then FS4 (cochlear implant)
Cochlear implant with tonotopy-based fitting then with default fitting
Sponsors
MED-EL Elektromedizinische Geräte GesmbH
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
DOUBLE (Subject, Investigator)
Masking description
Double blind study: The patient and the Investigator don't know the fitting.
Intervention model description
Crossover Assignment Two arms A and B: Arm A: Bimodal patient's fitting with default fitting (FS4) --\> 6 weeks use --\> tests and bimodal patient's fitting with tonotopy-based fitting (TFS4) --\> 6 weeks use --\> tests; Arm B: Bimodal patient's fitting with TFS4 --\> 6 weeks use --\> tests and bimodal patient's fitting with FS4 --\> 6 weeks use --\> tests
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adult patient (\>= 18 years old) speaking French * Patient who fulfils the criteria for cochlear implantation
Exclusion criteria
* retro-cochlear pathology: auditory neuropathy, vestibular schwannoma * patient with residual hearing \< 70 dB hearing level (HL) at 500 Hz and 1000 Hz on the contralateral ear
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Speech recognition in noise | at 6 weeks post-activation | The speech recognition in noise is evaluated with the French Matrix test (Framatrix) \[S. Jansen et al. Comparison of three types of French speech-in-noise tests: a multi-center study. Int J Audiol, 51 (3) (2012), pp. 164-173\]. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Speech recognition in quiet | at 6 weeks post-activation | Cochlear list of Lafon: list of 51 phonems (17 words). Speech recognition score on 50. |
| Auditory skills experienced by the patient | at 6 weeks post-activation | Auditory skills experienced by the patient are evaluated with the short form of the French version of the speech spatial qualities scale (SSQ) with of 15 questions describing various real-world auditory situations \[Moulin et al. Ear \& Hearing 2019;40;938-950\]. |
Countries
France
Contacts
CONTACTVincent Péan, PhD
PRINCIPAL_INVESTIGATORAlexandre Karkas, Pr
Centre Hospitalier Universitaire de Saint Etienne
Outcome results
None listed