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Investigating Auditory Processing in the Users of Auditory Brainstem and Cochlear Implants

Investigating Auditory Processing in the Users of Auditory Brainstem and Cochlear Implants

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05810220
Enrollment
200
Registered
2023-04-12
Start date
2018-12-02
Completion date
2026-12-31
Last updated
2025-12-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Deafness

Brief summary

This is a basic investigational research study conducted with hearing impaired adults and children who use cochlear implant or auditory brainstem implant (ABI) devices. The study will evaluate different aspects of hearing and auditory processing in the users of implantable auditory devices.

Interventions

DEVICEElectrode-Neural Interface

Measurements taken from the electrode-neural interface will be used to guide elimination of poorly functioning ABI electrodes and improve speech perception outcomes.

Sponsors

Cochlear Americas
CollaboratorUNKNOWN
NYU Langone Health
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
2 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Hearing impaired adult and or child (above 2 years old) who uses ABIs or cochlear implants. * No diagnosis of any other communicative or cognitive disorder other than hearing impairment. The individual must be able to visit the lab in order to participate in behavioral and electrophysiological experiments. * Patients' implant device must have useable electrodes that do not result in uncomfortable or unpleasant non-auditory sensation.

Exclusion criteria

* Diagnosed cognitive or communicative disorders (other than hearing impairment) * Severe neurological disorders * No useable electrodes in their implants

Design outcomes

Primary

MeasureTime frameDescription
Percent of Correctly-Identified Speech MaterialsDay 1 (Visit 1 - Average visit length is about 3 hours)Participants will listen to speech sounds and indicate what sentence or word they heard. The outcome is the percent of speech sounds that are correctly identified.
Percent of Correctly-Identified Stimuli Characteristics when Two or More Stimuli are PresentedDay 1 (Visit 1 - Average visit length is about 3 hours)Two or more stimuli will be presented to participants, who will indicate which one is louder, which is higher pitched, or which one is different. The outcome is the percent of stimuli characteristics that are correctly identified.

Countries

United States

Contacts

Primary ContactMahan Azadpour
Mahan.Azadpour@nyulangone.org2122637785

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026