- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04509024
Incidental Auditory Category Training for Language Learning (IACT)
July 23, 2024 updated by: Seth Wiener, Carnegie Mellon University
Examining the Impact of Non-linguistic Incidental Auditory Category Training on Adult Language Acquisition
The overarching goal of the proposed research is to understand how human listeners learn speech categories.
The project takes a prospective approach with adult second-language learners, blending empirical, methodological and theoretical advances from laboratory studies with explicit classroom instruction.
The central hypothesis is that incidentally-acquired nonlinguistic perceptual building block categories may support speech perception and production in a second language.
The project will advance important theoretical debates about the cross-talk between general auditory representations and speech categories and will provide a novel approach to nudging adult learners off learning plateau typically encountered in classroom instruction.
Study Overview
Status
Terminated
Detailed Description
Robust speech communication requires that listeners learn linguistically-relevant representations for stable language regularities, such as the speech sounds (phonemes) that convey meaning.
In an increasingly multilingual society, as many as twenty percent of Americans accomplish this across multiple languages.
Yet, second language acquisition is especially challenging among adult language learners, for whom learning typically involves explicit classroom instruction.
Troublingly, research documents that instruction routinely results in a 'learning plateau' whereby language abilities stagnate or even atrophy despite continued instruction.
There is a need to establish effective new approaches to nudge adult language learners off this plateau.
This project integrates theoretical and methodological developments in auditory category learning with approaches to classroom-based L2 instruction.
Specifically, incidental category learning (in which learners' attention is directed away from to-be-learned categories by an engaging videogame) taps into category learning systems distinct from those engaged in more explicit learning.
Moreover, incidental learning of nonspeech sound categories leads to activation of putatively speech-selective cortex associated with speech categorization, suggesting potential representational cross-talk.
This guides the central hypothesis of the project: incidental learning of nonspeech perceptual building block categories may provide a 'back door' through which to influence adult L2 learners' speech acquisition and to move them off the classroom learning plateau.
An intensive 8-week incidental training study will test the hypothesis (Aim 1).
Comparison of incidental nonspeech training with explicit L2 speech training will assess whether this cognitive 'back door' may be more effective in promoting L2 speech perception and production than explicit training with L2 speech and will determine the extent to which each interacts with classroom instruction in the L2 (Aim 2).
The results will reveal whether nonspeech, auditory categories sharing common perceptual dimensions with second language categories scaffold L2 acquisition, the degree to which explicit instruction may support or interfere with new auditory categories, whether incidental learning is retained after training, and whether learning gains transfer to support other language-learning tasks.
In blending empirical, methodological, and theoretical advances from laboratory studies with explicit classroom learning it will be possible to determine the interplay between incidentally-acquired nonlinguistic perceptual building block categories and an emerging L2.
This will advance important theoretical debates about the cross-talk between general auditory representations and speech categories and will provide a novel approach to L2 pedagogy.
Study Type
Interventional
Enrollment (Actual)
106
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 Locations
-
-
Pennsylvania
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Pittsburgh, Pennsylvania, United States, 15213
- Carnegie Mellon University
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- 18 or older, normal hearing
- Native/non-native Chinese speakers
Exclusion Criteria:
- Younger than 18, loss of hearing
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: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Incidental training
Participants undergo novel non-linguistic incidental category learning training.
|
Training involving non-speech sounds embedded in a video-game.
|
|
Experimental: Explicit training
Participants undergo traditional explicit language learning.
|
Training involving explicit sound and category information
|
|
No Intervention: No training
Participants do not undergo any training.
|
|
|
Experimental: Classroom training
Participants take part in structured classroom learning.
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Structured adult classroom language training.
|
|
Experimental: Classroom and incidental training
Participants take part in structured classroom learning and incidental learning.
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Both classroom and incidental training.
|
|
Experimental: Classroom and explicit training
Participants take part in structured classroom learning and explicit learning.
|
Both classroom and explicit training.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Sensitivity (D-prime) to Novel Speech Sounds After 2 Months of Training
Time Frame: Pre-test (baseline) and immediately after 2 months of training.
|
Each participant's 96 auditory discrimination data points at Pre-test and Post-test, respectively, were reduced to one sensitivity score: d-prime (d': hits minus false alarms).
This transformation takes into account response bias and approaches a normal distribution.
A higher score represents greater sensitivity.
The difference in scores from pre- to post-test represents the change.
|
Pre-test (baseline) and immediately after 2 months of training.
|
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Change in Auditory Category Learning Accuracy After 2 Months of Training
Time Frame: Pre-test (baseline) and immediately after 2 months of training.
|
Each participant's 96 auditory categorization data points at Pre-test and Post-test, respectively, were turned into a mean of the correct answers.
The difference between the two accuracy scores represents the mean change in accuracy.
|
Pre-test (baseline) and immediately after 2 months of training.
|
|
Novel Auditory Word Learning Accuracy After 2 Months of Training
Time Frame: Immediately after 2 months of training.
|
At post-test, participants did a three day novel word learning task.
Their 48 word identification data points on the first and third days, respectively, were turned into a mean correct score.
The difference in scores from Day 1 to Day 3 represents the change in mean novel word learning accuracy.
|
Immediately after 2 months of training.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Word Recognition Accuracy in Unrelated Language 3 Months After Training
Time Frame: 3 months post-intervention
|
Three months after training, participants were scheduled to learn words in an unrelated language.
Their mean accuracy would be calculated.
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3 months post-intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Seth Wiener, PhD, Carnegie Mellon University
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)
September 1, 2019
Primary Completion (Actual)
November 1, 2022
Study Completion (Actual)
January 10, 2023
Study Registration Dates
First Submitted
August 6, 2020
First Submitted That Met QC Criteria
August 10, 2020
First Posted (Actual)
August 11, 2020
Study Record Updates
Last Update Posted (Actual)
July 24, 2024
Last Update Submitted That Met QC Criteria
July 23, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Participants who have agreed to share their behavioral responses and speech recordings will have their data anonymized and shared via a free, open platform like OpenScience after completion of the study.
IPD Sharing Time Frame
Anonymized behavioral data available permanently via the Open Science Framework.
IPD Sharing Access Criteria
Available via Open Science Framework link
IPD Sharing Supporting Information Type
- ANALYTIC_CODE
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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