Actively Recruiting

Age: 18Years - 85Years
All Genders
ID07114744

Early Cochlear Implant Use

Led by NYU Langone Health · Updated on 2025-08-11

25

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

Sponsors

N

NYU Langone Health

Lead Sponsor

N

National Institute on Deafness and Other Communication Disorders (NIDCD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research focuses on adults using cochlear implants, specifically studying how their ability to distinguish simple sounds changes and relates to improved speech understanding. It aims to measure and describe these changes over the first year after cochlear implant activation, including both new users and those experienced with the same stimulation strategy. The study is observational and seeks to quantify progress in sound perception and speech comprehension during early implant use. Participants will complete about 25 test sessions at home during the first three months after cochlear implant activation using take-home computers and test equipment. These tests assess how well they can discriminate sounds varying in frequency and timing. After this home testing period, participants will visit the laboratory for three additional tests up to one year post-activation to track continued changes in speech perception. During the study, participants will undergo repeated speech perception tests to measure changes in their correct responses from baseline to one year. Researchers will monitor progress through self-completed home tests and lab visits. The total participation time includes the initial three months of frequent testing followed by periodic assessments up to one year after implant activation, allowing detailed observation of hearing improvements over time.

CONDITIONS

Brief Title

Early Cochlear Implant Use

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 85 years
  • Postlingually deaf cochlear implant users
  • Severe or profound hearing loss
  • No other diagnosed communicative or cognitive disorders
  • New users with no prior cochlear implant experience
  • Users who have used the same stimulation strategy since initial activation without ongoing improvements
Not Eligible

You will not qualify if you...

  • Diagnosed cognitive or communicative disorders other than deafness
  • Younger than 18 years
  • Older than 85 years

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Approximately 3 months

Participants complete take-home tests to assess speech perception improvement over time.

About 25 self-completed test sessions at home

Trial Site Locations

Total: 1 location

1

NYU Langone Health

New York, New York, United States, 10016

Actively Recruiting

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Research Team

A

Ariel E. Hight, PhD

M

Mario A. Svirsky, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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