- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06737185
Comparison of Speech Understanding Between Tonotopy-based Fitting and Setting Based on Evolutionary Algorithms
Comparison of Speech Understanding Between Tonotopy-based Fitting and Evolutionary Algorithm-based Setting: a Prospective Cross-sectional Study
Main objective:
Compare speech recognition in noise with tonotopic setting (FS4T) and with tonotopic fitting modified by evolutionary algorithm (EAFS4T) in adult patients implanted for 6 months or more with a MED-EL cochlear implant with FS4T.
Secondary objectives:
Comparison of FS4T and EAFS4T settings
- for speech recognition in quiet
- for subjective auditory spatial perception
- for subjective auditory and musical perception
Study Overview
Status
Conditions
Intervention / Treatment
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. The fitting software developed by the manufacturers proposed a default fitting with a lower limit between 100 and 250 Hz according to the brands and an upper limit of about 8500 Hz. The frequency bands assigned to each electrode follow a logarithmic scale with the high frequencies for the basal electrodes and the low frequencies for the apical electrodes. This distribution takes into account the number of active electrodes but does not take into account the anatomy and the natural cochlear tonotopy specific to each patient. Several studies have analyzed the anatomical variations of the cochlear dimensions: size of the cochlea and the ratio between the contact surfaces of the electrodes with the cochlea are variable from one patient to another. The insertion depth during surgery is also variable due to parameters related to the patients as well as to the operator, which seems to impact the understanding of speech in noise. Mathematical algorithms have recently been developed to estimate the cochlear tonotopy of each patient from a CT scan assessment. CT imaging of the implanted ear combined with 3D reconstruction software, provides cochlear length measurements Using this approach it is possible to measure the position of each electrode relative to the cochlear apex. Recently, MED-EL (Austria) has developed a new approach based on CT-scan and tuning of the frequencies associated with each electrode using anatomical information of position of the electrodes in the cochlea: this fitting is called anatomy-based fitting.
A tonotopy-based fitting allows for better results in pitch perception or speech perception in noise or musical perception. However, there is a large variability in the results observed between patients. This variability could be due to the individual characteristics of the listeners (neuronal survival, current propagation and spread, duration of deafness, lack of cortical plasticity).
A modification of frequency allocations in the setting could take into account this individual variability and improve speech discrimination and music perception. Saadoun et al. (2022) studied on 27 subjects the effect of an adjustment of frequency allocation by an evolutionary algorithm (EA) approach and showed an improvement in speech perception in noise compared to a default setting (not based on tonotopy) for patients implanted for more than 6 months in a bimodal situation (with a contralateral prosthesis). We therefore propose to use evolutionary algorithms to modify the tonotopy-based fitting and improve the perception in noise of implanted patients.
Main objective:
Compare speech recognition in noise with tonotopic setting (FS4T) and tonotopic fitting modified by evolutionary algorithm (EAFS4T) in adult patients implanted for 6 months or more with a MED-EL cochlear implant with FS4T.
Secondary objectives:
Comparison of FS4T and EAFS4T settings
- for speech recognition in quiet
- for subjective auditory spatial perception
- for subjective auditory and musical perception
Plan of the study: It is a prospective open monocentric transversal study.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Vincent Péan, PhD
- Phone Number: +33 603592974
- Email: vincent.pean@medel.com
Study Locations
-
-
-
Dijon, France, 21000
- Recruiting
- CHU
-
Contact:
- Alexis BOZORG GRAYELI, Pr
- Phone Number: 0380293758
- Email: alexis.bozorggrayeli@chu-dijon.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: EA arm
at 6 month post-activation: evolutionary algorithms to modify the tonotopy-based fitting FS4T to give EAFS4T fitting. Participant wears EAFS4T during 6 weeks. |
Comparison of FS4T and EAFS4T
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Speech recognition in noise
Time Frame: 6 weeks after EAFS4T fitting
|
HINT-5 min test. Noise level: 60 dB SPL. Speech level: adaptive with the answers of the participant. Result: speech-to-noise ratio (speech reception threshold, SRT50) for 50% of intelligibility in noise. Test with EAFS4T and with FS4T. |
6 weeks after EAFS4T fitting
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Speech recognition in quiet
Time Frame: 6 weeks after EAFS4T fitting
|
One list of 10 disyllabic words (Fournier lists) at 65 dB SPL. The participant has to repeat the word emitted. Result: score on 10. Test with EAFS4T and with FS4T |
6 weeks after EAFS4T fitting
|
|
Subjective auditory spatial perception
Time Frame: at EAFS4T fitting (6 months after cochlear implant activation) and 6 weeks after EAFS4T fitting
|
SSQi15 questionnaire (" Speech, Spatial, and Qualities of hearing scale ", SSQ). The questionnaire consists of 15 questions describing various real-world hearing situations. The subject answers each question with a score on a visual analogue scale graduated from 0 to 10 ranging from "not at all" to "yes perfectly". The result obtained is composed of
Questionnaire with FS4T (at EAFS4T fitting) and with EAFS4T (6 weeks after EAFS4T fitting) |
at EAFS4T fitting (6 months after cochlear implant activation) and 6 weeks after EAFS4T fitting
|
|
Subjective assessment of auditory perception
Time Frame: at EAFS4T fitting (6 months after cochlear implant activation) and 6 weeks after EAFS4T fitting
|
Assessment of sound quality in silence and in noise with 4 statements. Likert scale from 1 to 5. Score on 20. Likert scale with FS4T (at EAFS4T fitting) and with EAFS4T (6 weeks after EAFS4T fitting) |
at EAFS4T fitting (6 months after cochlear implant activation) and 6 weeks after EAFS4T fitting
|
|
Subjective assessment of musical perception
Time Frame: at EAFS4T fitting (6 months after cochlear implant activation) and 6 weeks after EAFS4T fitting
|
Six questions from the Munich Music Self-Questionnaire [Stark et al. 2003].
Questionnaire with FS4T (at EAFS4T fitting) and with EAFS4T (6 weeks after EAFS4T fitting)
|
at EAFS4T fitting (6 months after cochlear implant activation) and 6 weeks after EAFS4T fitting
|
Collaborators and Investigators
Investigators
- Principal Investigator: Alexis BOZORG GRAYELI, Pr, Centre Hospitalier Universitaire Dijon
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MEDEL_algoevIC_Dijon_study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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