Spatial Hearing Perception in Bilateral Cochlear Implant Children (SPHERIC1)

December 13, 2025 updated by: Hospices Civils de Lyon

Spatial hearing in cochlear implant (CI) users is a challenging investigation field since no studies have explored yet spatial auditory perception in three-dimensional space (3D). Moreover auditory rehabilitation after cochlear implantation is totally devoted to speech rehabilitation to date.

A novel methodology based on virtual reality and 3D motion capture protocol in an immersive reality system has recently been developed to evaluate and record spatial hearing abilities of norm-hearing (NH) listeners and CI adults in 3D. The results revealed worse sound localization in 3D for CI users compared to NH participants, and interestingly noted that head movements could improve sound localization performances, leading to a possible track for auditory rehabilitation.

The aim of this study is to explore spatial hearing in CI children with the protocol already tested in CI adults. This protocol will be adapted to children over eight years old. Children will have to perform a sound localization task in 3D without any feedback of performances. The knowledge improvement in pediatric sound localization will lead to develop a specific spatial rehabilitation in cochlear implant children.

Study Overview

Study Type

Interventional

Enrollment (Actual)

36

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Bron, France, 69676
        • Centre de Recherche en Neuroscience de Lyon (CRNL)
      • Lyon, France, 69437
        • Hôpital Edouard Herriot

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

4 years to 13 years (Child)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria for cochlear implant children:

  • Age between 8 and 17 included
  • second cochlear implant issued within more than 2 years
  • mean speech recognition over 80% with two cochlear implants
  • normal visual acuity with or without correction
  • abilities to understand experimental instructions
  • a consent form signed by parents or guardian
  • registered with a social security scheme

Exclusion Criteria for cochlear implant children:

  • neurologic or psychiatric trouble
  • visual trouble
  • bilateral vestibular areflexia

Inclusion Criteria for normal hearing children:

  • Age between 8 and 17 included
  • normal visual acuity with or without correction
  • abilities to understand experimental instructions
  • a consent form signed by parents or guardian
  • registered with a social security scheme

Exclusion Criteria for normal hearing children:

  • neurologic or psychiatric trouble
  • visual trouble
  • bilateral vestibular areflexia

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: cochlear implant children
18 cochlear implant children wil include in this study

Normal hearing children and cochlear implant children will have to localize a sound source in three dimensional space by using a virtual reality system (Neuro immersion platform). The experiment will last thirty minutes.

For normal hearing children, this experience will be performed at the inclusion visit.

For cochlear implant children, this experience will be performed 28 days (+/- 2 days) after inclusion.

For cochlear implant children and their parents, a SSQ questionnaire will be given and completed during the first visit (at the inclusion).

This questionnaire offers a version for parents of children with hearing loss ("SSQ Parents CI") and a version for the children themselves ("SSQ Children CI").

The SSQ questionnaire for Parents of CI children is composed of three distinct sections (A, B and C).

Each section will be filled separately by parents of CI children with one of the study collaborators during 3 telephone calls spaced 1 week apart. Thus, section A will be completed 7 days (+/- 2 days) after inclusion , section B 14 days (+/- 2 days) after inclusion, and section C 21 days (+/- 2 days) after inclusion.

Other: normal hearing children
18 normal hearing children wil include in this study

Normal hearing children and cochlear implant children will have to localize a sound source in three dimensional space by using a virtual reality system (Neuro immersion platform). The experiment will last thirty minutes.

For normal hearing children, this experience will be performed at the inclusion visit.

For cochlear implant children, this experience will be performed 28 days (+/- 2 days) after inclusion.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
measure of the spatial hearing deficit matching the distance between the hand pointing error and the sound source position in space
Time Frame: thirty minutes
Data from spatial sound perception will be recorded in three dimensional space (azimuth, elevation, and depth). First, the pointing error will be computed separately for azimuth, elevation, and depth, in terms of constant error (absolute and signed) and variable error. Then, these separate errors will be combined into a cumulative error "D", hence summarizing all three dimensions of space, and taking into account absolute and variable error in one measure.
thirty minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
measure of head and eye movements in three dimensional space with a motion tracking system (virtual reality system including a Head-Mounted display) to evaluate their roles in spatial hearing performances.
Time Frame: thirty minutes
Head and eye movements will be recorded in three dimensional space with a motion tracking system (virtual reality system including a Head-Mounted display). The cumulative error "D" will be calculated in two different conditions: first, participant's head will be fixed during sound emission and then, head and eyes will be free to move. If the cumulative error "D" significantly decreases when head movements are free, we could say that head movements allow/help improving spatial hearing performances.
thirty minutes
impact of age at cochlear implantation on spatial hearing deficit
Time Frame: thirty minutes
spatial hearing deficit will be correlated to the age at cochlear implantation
thirty minutes
change of the pupil diameter during a sound localization task
Time Frame: thirty minutes
Pupil diameter will be recorded with an eye tracking system during all experiment
thirty minutes
correlation between a clinical score (SSQ) and sound localization performances
Time Frame: 28 days
The SSQ questionnaire is a clinical subjective scale adapted to parents and cochlear implant children. It allows evaluating hearing performances in daily life. The questionnaire is divided into 3 main items (A: speech; B: spatial hearing; C: other qualities of hearing) comprising questions with rating scores out of ten. For example, a zero score corresponds to bad hearing abilities. We will therefore correlate the mean score of all questions out of ten to the cumulative error "D".
28 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Eric TRUY, PUPH, Hospices Civils de Lyon

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 24, 2019

Primary Completion (Actual)

November 18, 2019

Study Completion (Actual)

November 18, 2019

Study Registration Dates

First Submitted

October 8, 2018

First Submitted That Met QC Criteria

November 8, 2018

First Posted (Actual)

November 13, 2018

Study Record Updates

Last Update Posted (Estimated)

December 19, 2025

Last Update Submitted That Met QC Criteria

December 13, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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