Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
Healthy Volunteers
NCT04733950

Cochlear Implanted Listening Effort and Hearing Attention

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-01-13

170

Participants Needed

1

Research Sites

219 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Cochlear implant users perceive mainly sound amplitude modulation cues. Processing of these amplitude modulations can be subject to interferences, so that the perception of a modulation in a target sound can be impaired by a superimposed sound if this sound contains a similar modulation. Such phenomenon, which is observed both in subjects with normal-hearing and in cochlear-implant users, could be explained by difficulties to direct attention to relevant information in complex sound signals. Selective auditory attention also plays a crucial role in speech comprehension in cocktail-party situations where the speech of multiple talkers get mixed at the ear of a listener. Cochlear implant users typically struggle in these cocktail-party situations and report intense listening effort. The present clinical trial aims at evaluating the contribution of selective auditory attention for sound modulations to the listening effort of patients with cochlear implants and of healthy volunteers with normal-hearing during speech perception under cocktail-party-like conditions. Selective auditory attention abilities of patients and controls will be assessed using a psychoacoustical test whereby their ability to detect a target sound amplitude modulation will be measured both in the absence and in the presence of an interfering (i.e. distracting) amplitude modulation occurring in a distant spectral region from that of the target. The effect of this distractor's presence on modulation detection performance will serve as a behavioural index of the subject's auditory attention capacities. The attentional capacity index will then be tested as a predicting factor for the listening effort of the subject during a speech-in-noise consonant identification task. Listening effort will be measured from the pupil dilation response to the presented speech units (pseudowords). This study will enhance our understanding of cochlear implant user's perception and listening effort and will serve as a basis for prognostic tests of listening effort and of implantation success for cochlear implant candidates, based on a simple measurement of auditory attentional abilities.

CONDITIONS

Official Title

Cochlear Implanted Listening Effort and Hearing Attention

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 80 years old
  • Mother tongue is French
  • Normal vision with or without correction
  • No eye diseases such as cataracts, nystagmus, amblyopia, or macular degeneration
  • Not taking psychotropic drugs or drugs affecting the parasympathetic nervous system
  • No history of neurological diseases such as head trauma or stroke
  • Signed informed consent before participation
  • For cochlear implant patients: having a unilateral Oticon Medical cochlear implant used for 6 months or more
  • For cochlear implant patients: disyllabic word recognition score of at least 40% on average in silence
  • For cochlear implant patients: disyllabic word recognition score not exceeding 30% on the opposite ear alone, aided or not, in silence
  • For volunteers with normal hearing: confirmed normal tonal audiometry for age
Not Eligible

You will not qualify if you...

  • Eye diseases such as cataracts, nystagmus, amblyopia, or macular degeneration
  • Taking psychotropic drugs or drugs affecting the parasympathetic nervous system
  • Neurological diseases or history affecting cognitive function or eye movement stability
  • No social security affiliation or entitlement
  • Under State Medical Assistance
  • Under legal protection such as tutorship, curatorship, or family authorization

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Trial Site Locations

Total: 1 location

1

Assistance Publique-Hôpitaux de Paris

Paris, France, 75013

Actively Recruiting

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Research Team

I

Isabelle MOSNIER, MD

CONTACT

D

Dorothée ARZOUNIAN, Ph. D

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

FACTORIAL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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