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Impact of Microphone Positioning on Auditory Performance in Cochlear Implant Users (MICLO)

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Withdrawn

Conditions

Cochlear Prosthesis Implantation

Treatments

Behavioral: Likert scale
Behavioral: Quality of life questionnaire
Behavioral: French Matrix Test
Behavioral: SPHERE protocol
Device: Modification of active microphone positioning

Study type

Interventional

Funder types

Other

Identifiers

NCT04677517
69HCL20_1013

Details and patient eligibility

About

The construction of our auditory space requires several prerequisites, including localization abilities in 3D (azimuth, elevation and distance). These abilities rely on the proper development and functionality of the auditory system to extract various acoustic cues from our environment. Extraction and analysis of these auditory cues are based on the synchronous use of ears, called binaurality. Other natural behaviours are useful to precisely determine the location of a sound source: visual information and head movements.

The slightest anatomical-functional change (e.g. unilateral hearing loss, malformation of the pinna) can disturb spatial hearing abilities. Many patients with hearing loss are fitted with a hearing aid (HA) or a cochlear implant (CI) to ensure the best speech understanding. However, this auditory rehabilitation remains insufficient to restore a good perception of spatial hearing. One of the key point to improve sound localization seems to be microphone positioning on hearing aids. Several questions remain on the optimal microphone positioning.

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 to 75 inclusive
  • Regular follow-up in the Ear Nose and Throat department of the Edouard Herriot hospital in Lyon
  • Post-lingual deafness
  • Fitted with two Advanced Bionics (AB) cochlear implants (Naïda Q70 or Naïda Q90 processor) Or fitted with one AB cochlear implant and a contralateral hearing aid
  • Fitted with the latest implant for more than 1 year
  • Normal or corrected vision
  • Able to understand experimental instructions
  • Affiliated with a social security scheme

Exclusion criteria

  • Oculomotor disorder
  • Bilateral vestibular areflexia
  • Adult subject to a legal protection measure (guardianship, curatorship)

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Implanted patients
Experimental group
Description:
All the participants are patients with post-lingual deafness and fitted with cochlear implants
Treatment:
Device: Modification of active microphone positioning
Behavioral: SPHERE protocol
Behavioral: French Matrix Test
Behavioral: Quality of life questionnaire
Behavioral: Likert scale

Trial contacts and locations

1

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Central trial contact

Valérie GAVEAU, PhD; Eric TRUY, Professor

Data sourced from clinicaltrials.gov

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