Actively Recruiting
Role of Selective Attention for Sound Modulations in the Listening Effort of Patients With Cochlear Implants
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-01-13
170
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to understand how selective auditory attention affects listening effort in adults with cochlear implants compared to adults with normal hearing. It focuses on how these individuals perceive sound amplitude modulations, especially in challenging listening situations like cocktail parties where multiple voices mix. The study investigates how well participants can focus on important sound cues despite distracting modulations and how this relates to their effort when recognizing speech. Participants include adults with cochlear implants used for at least six months and healthy volunteers with normal hearing. The study involves psychoacoustic tests where participants detect target sound modulations amid distractions using a forced-choice task. Pupil diameter is measured to assess listening effort during speech perception tests, including recognition of consonants in silence and with interfering speech. Tests are done in a soundproof booth using specialized equipment and implant processors. Participants take part in a session lasting about 1 hour and 40 minutes, including consent, hearing tests, psychoacoustic tasks, and speech recognition with eye-tracking to measure pupil size. The study measures auditory attention capacity and listening effort, analyzing correlations between these factors. Results aim to improve understanding of cochlear implant users' hearing challenges and support development of prognostic tests for listening effort and implant success.
CONDITIONS
Brief Title
Cochlear Implanted Listening Effort and Hearing Attention
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 80 years
- 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 medications affecting the parasympathetic nervous system
- No neurological conditions like head trauma or stroke affecting cognitive functions or eye movements
- For cochlear implant patients: unilateral Oticon Medical 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% in the opposite ear, aided or not
- For healthy volunteers: normal tonal audiometry for their age
You will not qualify if you...
- Eye pathologies such as cataracts, nystagmus, amblyopia, or macular degeneration
- Taking psychotropic drugs or medications affecting the parasympathetic nervous system
- Neurological diseases or history affecting cognition or eye movement stability
- Not affiliated with a social security scheme or under State Medical Assistance
- Under legal protection such as tutorship, curatorship, or family authorization
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) for consent, eligibility confirmation, and baseline assessments
Duration - 1 session lasting approximately 1 hour and 40 minutes
Participants undergo a series of psychoacoustic tests and speech recognition tasks to evaluate auditory attention and listening effort. This includes amplitude modulation detection tasks and consonant identification tests with and without interfering speech.
1 in-person session, with a possible second session if tests are not completed
Trial Site Locations
Total: 1 location
1
Assistance Publique-Hôpitaux de Paris
Paris, France, 75013
Actively Recruiting
Research Team
I
Isabelle MOSNIER, MD
D
Dorothée ARZOUNIAN, Ph. D
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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