Perceptual Learning and Memory Consolidation in Adults With and Without LI

July 7, 2020 updated by: Frances Sayako Earle, University of Delaware

Perceptual Learning and Memory Consolidation in Adults With and Without Language Impairment

This study tests a memory-based account of atypical speech perception in adults with language-based learning disability (also known as developmental language impairment [LI]). One perspective regarding the its etiology considers impoverished speech sound representations to be central to the linguistic symptoms observed in LI. This project examines a potential abnormality in the process of building speech sound representations in LI.

Previous work by the PI has found that sleep is important for learning speech sounds. Furthermore, different measures of speech perception (identification and discrimination), reveal distinct patterns of learning that are consistent with that of declarative and procedural memory consolidation. A division of labor by declarative and procedural memory systems in the building of speech representations may imply that problems with phonology may stem from selective weaknesses in declarative or procedural memory in predictive ways.

The first project Aim is to identify the memory substrates of novel phonetic category formation. In Experiment 1, the investigators will obtain behavioral measures of declarative, procedural, and speech sound learning before and after post-training sleep in 40 typical adults and 20 adults with LI. Among typical adults, a double dissociation is predicted in which speech identification will be predicted by individual differences in declarative memory, and speech discrimination will be predicted by individual differences in procedural memory. Moreover, adults with LI are predicted to demonstrate consolidation deficits across memory types.

The second project Aim is to identify the neural substrates of phonetic category formation. In Experiment 2, the investigators will obtain functional magnetic resonance (fMRI) recordings of 20 TD and 20 LI adults performing post-training identification and discrimination tasks on a trained speech contrast before and after sleep. In typical adults, a Time by Speech-task interaction is predicted. Speech identification will recruit episodic (hippocampal) information on Day 1 relative to classic regions for phonological processing on Day 2. Speech discrimination will result in a change in magnitude of activation from Days 1 and 2 in the left inferior frontal gyrus (IFG), reflecting an overnight decrease in effort. LI (n=20) is predicted to demonstrate reduced overnight change in neural activation relative to TD in both tasks.

Study Overview

Status

Suspended

Intervention / Treatment

Detailed Description

The investigators will recruit 60 adults with typical language (TD) and 40 LI participants through a variety of community and university related contacts. 40 TD adults and 20 LI participants will be enrolled in Experiment 1. 20 TD adults and 20 LI participants will be enrolled in Experiment 2.

Both experiments will take place over 3 Sessions.

During Session 1, the investigators will administer various measures in order to validate study eligibility, classify participants into groups, and other measures in order to further characterize our samples. To that end, participants will be administered a pure tone audiometric screening, and complete an interview questionnaire asking for background information such as handedness, language background, language and reading development, and development of motor skills. Trained research personnel will then administer an approximately 2-hour testing battery that includes measures of nonverbal cognition, language ability, reading ability, attention, executive function, and phonological processing. Participants will also complete questionnaires to assess their habitual sleep quality, sleepiness, and individual chronotpyes.

All testing will be completed by a student clinician, and will be supervised by a certified speech-language pathologist. 100% of administrations will be re-scored by a trained student for accuracy. To account for attrition and non-qualifiers, we anticipate enrolling/screening up to 200 individuals in Session 1 in order to arrive at the enrollment targets for Experiments 1 and 2.

In both experiments, Sessions 2 and 3 takes place on two consecutive days. Session 2 will take place in the late evening, and Session 3 will take place in the morning. We have intentionally chosen not to employ a wake-state (AM-PM) control. This is done in order to limit the potential variability in the amount of English exposure between sessions. Between-session sleep duration will be monitored with an Actigraph wGT3X-BT accelerometer (Actigraph, corp) worn on the non-dominant wrist. Actigraphs will be set to collect data in 60-second epochs via a validated algorithm (Cain & Geremia,2011). This method of recording sleep/wake activity has been independently validated to agree with lab polysomnography at 85% accuracy (Slater et al.,2015).

Experiment 1: behavioral measures During Session 2, participants will complete the three learning tasks, declarative learning, procedural learning, nonnative speech learning (in that order), and immediate post-learning assessments. During Session 3, participants will be re-assessed in nonnative speech learning, declarative learning, and procedural learning (in that order).

  • Declarative memory will be assessed using an object recognition task following incidental encoding.
  • A version of the Serial Reaction Time task will be used to measure procedural learning.
  • Perceptual learning of speech will be measured through performance on identification and discrimination tasks on the dental and retroflex contrast.

Experiment 2: neuroimaging measures During Session 2, participants will complete the nonnative contrast training in the late evening. Then they will enter a magnetic resonance imagine (MRI) scanner, where their blood oxygen-level dependent signals will be recorded while they complete the post-training identification and discrimination assessments. The participants will complete the same in-scanner assessments of the perception of the nonnative contrast during Session 3.

Study Type

Interventional

Enrollment (Anticipated)

100

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

    • Delaware
      • Newark, Delaware, United States, 19713
        • University of Delaware

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 to 24 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion criteria:

  • Monolingual speakers of American English
  • History of:

    • Typical gestation
    • Sensory-motor development
    • Typical hearing and vision
    • Nonverbal cognition within normal limits

Exclusion criteria:

  • Current diagnosis of ADHD
  • Developmental dyslexia
  • Rapid automatized naming deficits
  • Neurological disorders
  • Socio-emotional disorders

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: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: behavioral
Adults with and without language impairment will be given three different types of behavioral training, and assessments of learning through those trainings, at two time points.
the participants will be trained to perceive a non-native speech contrast
EXPERIMENTAL: neuroimaging
Following speech sound behavioral training, adults with and without language impairment will undergo post-training perceptual assessments in an MRI scanner before and after post-training sleep.
the participants will be trained to perceive a non-native speech contrast

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
nonnative speech sound learning: behavioral measures of memory consolidation
Time Frame: 2 days
learning will be assessed via behavioral performance (accuracy transformed to d') on perceptual tasks before training, after training, and after a post-training period of sleep
2 days
nonnative speech sound learning: fMRI measures of memory consolidation
Time Frame: 2 days
change over a period of sleep in neural activation (BOLD response) in response to learned speech
2 days

Collaborators and Investigators

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

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)

August 1, 2018

Primary Completion (ANTICIPATED)

March 1, 2021

Study Completion (ANTICIPATED)

July 31, 2021

Study Registration Dates

First Submitted

June 28, 2018

First Submitted That Met QC Criteria

July 24, 2018

First Posted (ACTUAL)

August 1, 2018

Study Record Updates

Last Update Posted (ACTUAL)

July 9, 2020

Last Update Submitted That Met QC Criteria

July 7, 2020

Last Verified

July 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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