Recognition of Second Language Spoken Words, Signs, and Characters Via Perception and Production in Adults

October 17, 2022 updated by: University of Alabama, Tuscaloosa

How Motor Cortex Supports L2 Acquisition of Spoken Words, Signs, and Characters Via Perception and Production

Self-production facilitates acquisition of spoken words, signs, and characters from an unfamiliar second language. The proposed work investigates how motor cortex, a key part of the brain enabling body action, supports their acquisition via production as well as perception, providing insight into whether they are learned via mental simulation of the body actions used to produce them. It is hypothesized that activity in motor cortex will differ based on the body part used to produce lexical items (e.g., mouth vs. hands), will be greater for lexical items learned via production than observation, and will differentiate lexical items recognized successfully vs. unsuccessfully.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

120

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: Laura Morett, Ph.D.
  • Phone Number: 205-348-8489
  • Email: lmorett@ua.edu

Study Locations

    • Alabama
      • Tuscaloosa, Alabama, United States, 35487
        • University of Alabama, Tuscaloosa

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

16 years to 33 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Right-handed
  • Native English speaker

Exclusion Criteria:

  • Knowledge of sign language or languages with logographic characters
  • Hearing or vision impairments
  • Speech, language, or learning disorders
  • Unsecured metal body implants

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: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Self-production
L2 lexical items self-produced at learning
After participants learn L2 lexical items via hearing or observing them paired with L1 translations, they are prompted to produce them themselves
Active Comparator: Perception
L2 lexical items heard or observed an additional time at learning
After participants learn L2 lexical items via hearing or observing them paired with L1 translations, they are prompted to produce them themselves

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Functional activity in motor cortex location, 5 min, recognition
Time Frame: 5 minutes after learning
Location of Blood Oxygen Level Dependent (BOLD) signal in motor cortex at recognition
5 minutes after learning
Functional activity in motor cortex degree, 5 min, recognition
Time Frame: 5 minutes after learning
Degree of Blood Oxygen Level Dependent (BOLD) signal in motor cortex at recognition
5 minutes after learning
Functional activity in motor cortex location, 1 week, recognition
Time Frame: 1 week after learning
Location of Blood Oxygen Level Dependent (BOLD) signal in motor cortex at recognition
1 week after learning
Functional activity in motor cortex degree, 1 week, recognition
Time Frame: 1 week after learning
Degree of Blood Oxygen Level Dependent (BOLD) signal in motor cortex at recognition
1 week after learning

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Laura Morett, Ph.D., University of Alabama, Tuscaloosa

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 (Anticipated)

August 23, 2023

Primary Completion (Anticipated)

May 8, 2026

Study Completion (Anticipated)

May 8, 2026

Study Registration Dates

First Submitted

September 30, 2022

First Submitted That Met QC Criteria

October 17, 2022

First Posted (Actual)

October 20, 2022

Study Record Updates

Last Update Posted (Actual)

October 20, 2022

Last Update Submitted That Met QC Criteria

October 17, 2022

Last Verified

September 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • L2WordProd

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Plan Description

All individual participant data (IPD) underlying results in publications (de-identified)

IPD Sharing Time Frame

Immediately upon publication

IPD Sharing Access Criteria

Publicly available

IPD Sharing Supporting Information Type

  • Study Protocol
  • Statistical Analysis Plan (SAP)
  • 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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