Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
ID06465979

Perception of Speech in Context by Listeners With Healthy and Impaired Hearing

Led by Marquette University · Updated on 2026-06-03

680

Participants Needed

2

Research Sites

4 weeks

Total Duration

On this page

Sponsors

M

Marquette University

Lead Sponsor

N

National Institute on Deafness and Other Communication Disorders (NIDCD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating how people with normal hearing, hearing loss, or cochlear implants recognize speech sounds within the context of surrounding sounds. The study aims to understand how the frequency and timing of nearby sounds affect speech perception, especially under noisy conditions, and how these processes differ in listeners with hearing impairments. The research includes using computer models to simulate neural responses to speech sounds in context. Participants listen to speech played at comfortable volumes inside a sound booth and respond by identifying what they hear, either by speaking or choosing from options on a computer. The speech sounds are systematically modified in various ways, such as changing frequencies, speaking rates, or simulating hearing loss effects. These manipulations help researchers study how surrounding sounds influence speech recognition. Participants complete several testing blocks with breaks offered, and assignment to testing conditions is randomized. Throughout the study, participants provide responses at their own pace with minimal intervention. Researchers measure speech categorization and word recognition during testing, along with initial hearing assessments. The main outcome is how well participants identify speech sounds after these systematic manipulations. After completing all testing, participants are informed about the study's full purpose and findings. The study typically lasts about one year from enrollment to final data reporting.

CONDITIONS

Brief Title

Perception of Speech in Context by Listeners With Healthy and Impaired Hearing

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be able to recognize spoken words in English
  • Be a competent speaker of North American English
  • Be an adult between the age of 18 to 65 years
  • Have normal audiometric thresholds below 25 decibels hearing loss (dB HL) at frequencies between 250 and 8000 Hz OR have audiometric thresholds not exceeding 40 dB HL at frequencies between 250 and 8000 Hz OR have audiometric thresholds not exceeding 55 dB HL at frequencies between 250 and 8000 Hz OR use a cochlear implant
  • Lack language-learning or other cognitive disabilities
Not Eligible

You will not qualify if you...

  • Inability to recognize spoken words in English
  • Not a competent speaker of North American English
  • Be younger than 18 years of age
  • Be older than 65 years of age
  • Have normal audiometric thresholds exceeding 25 dB HL at frequencies between 250 and 8000 Hz OR have audiometric thresholds exceeding 40 dB HL at frequencies between 250 and 8000 Hz OR have audiometric thresholds exceeding 55 dB HL at frequencies between 250 and 8000 Hz
  • Language-learning or other cognitive disabilities

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)

Outpatient Treatment

Duration - 1 day

Participants listen to speech played at a comfortable volume inside a sound booth and respond by indicating what they heard. They complete testing blocks that include various speech sound manipulations and speech recognition tasks, with breaks offered between blocks.

1 to 2 visits depending on testing blocks

Long-term Monitoring

Duration - Up to 1 year

Participants' speech categorization and recognition outcomes are assessed and reported through study completion, averaging 1 year following the testing session.

Follow-up assessments as scheduled

Trial Site Locations

Total: 2 locations

1

University of Minnesota

Minneapolis, Minnesota, United States, 55455

Actively Recruiting

2

Marquette University

Milwaukee, Wisconsin, United States, 53233

Actively Recruiting

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Research Team

C

Christian Stilp, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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Frequently Asked Questions

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