- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05435989
Extended High-frequency Hearing and Speech Perception
May 8, 2023 updated by: Brian Monson
This study examines the effects of low-pass filtering speech on speech perception.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
480
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Brian Monson, PhD
- Phone Number: 217-300-6212
- Email: monson@illinois.edu
Study Locations
-
-
Illinois
-
Champaign, Illinois, United States, 61820
- Recruiting
- University of Illinois Urbana-Champaign
-
Contact:
- Brian Monson, PhD
- Phone Number: 217-300-6212
- Email: monson@illinois.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
19 years to 50 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- native speakers of American English
- normal hearing 250-8000 Hz
Exclusion Criteria:
- non-native speakers of American English
- hearing loss
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
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: Normal-hearing listeners
|
This study examines the effects of low-pass filtering speech on speech perception.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Speech recognition or localization score
Time Frame: Day 1
|
Speech recognition or localization scores are assessed using alternative forced choice procedures implemented with custom software scripts (e.g. in Matlab)
|
Day 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 9, 2021
Primary Completion (Anticipated)
June 1, 2026
Study Completion (Anticipated)
June 1, 2026
Study Registration Dates
First Submitted
June 16, 2022
First Submitted That Met QC Criteria
June 22, 2022
First Posted (Actual)
June 28, 2022
Study Record Updates
Last Update Posted (Actual)
May 10, 2023
Last Update Submitted That Met QC Criteria
May 8, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- AH181
- R01DC019745 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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