- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06465979
Perception of Speech in Context by Listeners With Healthy and Impaired Hearing
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Participants in this study listen to speech played at a comfortable volume and respond by indicating what they heard, either in open-ended form or by choosing among a set of options displayed on a computer. They are seated inside a sound booth and complete the task at their own pace, with little intervention needed from the experimenter. Upon arrival at the lab, participants are given a brief description of the topic of the research (how earlier sounds influence our perception of later speech sounds) and are presented with a detailed informed consent form. Their demographic information is collected and then the experiment is demonstrated. Breaks are offered between testing blocks, which last about 10-15 minutes each.
The main differences in the protocol consist of the various stimulus manipulations, which are designed to specifically control aspect of the voice that the participant hears. For example, the sound can be manipulated to emphasize higher or lower frequencies, or be spoken relatively slowly or quickly, or manipulated to sound degraded, as if the participant has a hearing loss. In all occasions, the manipulations are signaled to the participant. The outcome measure typically consists of the pattern of word identification, and specifically how that pattern changes depending on acoustic properties of the sounds heard before the target word.
Additional comparison measurements are taken of the participant's ability to hear and repeat words or sentences in background noise.
Once an experiment is ready to launch, participants are randomly assigned to different testing conditions ("interventions"). But in most of the planned experiments, participants complete identical protocols, except that the specific ordering of many speech stimuli is randomized within the testing session. After the participant completes all of the testing blocks, they are debriefed about the full nature of the study, the hypotheses and the larger scope of the project in the context of speech communication.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Christian Stilp, PhD
- Phone Number: 4142881455
- Email: christian.stilp@marquette.edu
Study Locations
-
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Minnesota
-
Minneapolis, Minnesota, United States, 55455
- Recruiting
- University of Minnesota
-
Contact:
- Matthew Winn, PhD, AuD
-
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Wisconsin
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Milwaukee, Wisconsin, United States, 53233
- Recruiting
- Marquette University
-
Contact:
- Christian Stilp, PhD
- Phone Number: 4142881455
- Email: christian.stilp@marquette.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Speech perception experiments
This arm involves experiments wherein participants listen to speech played at comfortable volumes and respond by indicating what they heard either in open-ended form or by choosing among a set of options displayed on a computer.
|
The acoustic properties of speech sounds will be modified in two main ways.
The first way is to introduce gradual changes to the perceived articulation of the target speech sound, such as changing from "sh" to "s" by various types of signal processing and filtering.
The second type of change is to modify acoustic properties of the sounds that immediately precede the target speech sound, such as changing the speaking rate or its frequencies composition.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Speech categorization
Time Frame: "Post-treatment" where "treatment" is the systematic manipulation of speech sounds. Speech categorization will be evaluated during the main part of the testing. Outcomes will be assessed and data reported through study completion, an average of 1 year
|
The participant sits inside a double-walled sound booth.
They are seated at a table that contains a computer monitor and a mouse.
A single utterance is played over headphones or through a loudspeaker directly in front, and the participant indicates what they thought the utterance was by selecting among various options on the screen using the mouse.
During a single block of trials there are between 60 and 160 sounds, depending on the exact experiment.
Ordering of stimuli within the block is randomized.
That testing block may be repeated multiple times so that the proportion of responses for each sound-response pair can be estimated reliably and precisely.
Completion and advancement of trials is at the participant's own pace.
Each testing block takes between 4 and 15 minutes.
|
"Post-treatment" where "treatment" is the systematic manipulation of speech sounds. Speech categorization will be evaluated during the main part of the testing. Outcomes will be assessed and data reported through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Speech recognition
Time Frame: "Post-treatment" where "treatment" is the systematic manipulation of speech sounds. Word recognition will be evaluated during the main part of the testing. Outcomes will be assessed and data reported through study completion, an average of 1 year
|
The participant sits inside a double-walled sound booth.
They are seated at a table that contains a computer monitor and a mouse.
Recorded sentences are played over headphones or through a loudspeaker directly in front, and the participant indicates what they thought the utterance was by typing their response or repeating the sentence aloud.
During a single block of trials there are 50 words.
Ordering of words within the block is randomized.
Completion and advancement of trials is at the participant's own pace.
Each testing block takes between 6 and 15 minutes.
|
"Post-treatment" where "treatment" is the systematic manipulation of speech sounds. Word recognition will be evaluated during the main part of the testing. Outcomes will be assessed and data reported through study completion, an average of 1 year
|
|
Audiometric threshold testing
Time Frame: Baseline
|
The participant sits inside a double-walled sound booth.
Under headphones, they listen for soft tones played by an audiometer.
The experimenter controls the timing, frequency and intensity of those tones to find the lowest sound intensity where the participant can detect the tone.
Thresholds for sound detection are recorded for octave frequencies between 250 Hz and 8000 Hz.
|
Baseline
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Christian Stilp, PhD, Marquette University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 4824
- R01DC020303 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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