Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
Healthy Volunteers
NCT07279441

Cochlear Implants and Listening Effort: the Interaction of Cognitive and Sensory Constraints

Led by NYU Langone Health · Updated on 2025-12-12

460

Participants Needed

2

Research Sites

260 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 study examines how cochlear implant users understand and comprehend speech in realistic communication situations. Through six experiments measuring listening effort via pupillometry and discourse comprehension, we will investigate how linguistic context, cognitive demands, and processing time affect speech understanding in CI users, and in normal-hearing controls) to identify factors underlying communication resilience versus vulnerability and develop improved, ecologically valid assessment and rehabilitation strategies.

CONDITIONS

Official Title

Cochlear Implants and Listening Effort: the Interaction of Cognitive and Sensory Constraints

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 80 years
  • Healthy normal-hearing or cochlear implant users
Not Eligible

You will not qualify if you...

  • Individuals under 18 years of age
  • Those with neurologic, vascular, psychiatric disease, dementia, or taking interfering medications
  • History of language disorders not related to hearing loss
  • Non-native speakers of American English

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Brandeis University

Waltham, Massachusetts, United States, 02453

Actively Recruiting

2

NYU Langone Health

New York, New York, United States, 10016

Actively Recruiting

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Research Team

M

Mario A. Svirsky, PhD

CONTACT

N

Nicole Capach

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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