KAWStory: Kindergarten Children Acquiring Words Through Storybook Reading

Sponsor
University of Kansas (Other)
Overall Status
Recruiting
CT.gov ID
NCT03586479
Collaborator
National Institute on Deafness and Other Communication Disorders (NIDCD) (NIH)
60
1
3
70
0.9

Study Details

Study Description

Brief Summary

Children with Specific Language Impairment (SLI) are slower to learn new words than their peers, placing them at risk for academic failure. In this study, we are improving a storybook reading treatment to help Kindergarten children with SLI learn new words. In this study, we compare three versions of book reading that vary in how often children are tested on, meaning asked to talk about, the words they are learning in the book: low vs. mid vs. high testing. We then examine which version of the treatment leads to better learning of the words during treatment and remembering of the words after treatment. We also seek to understand individual differences in treatment outcomes by examining pre-treatment predictors as well as progress during and after treatment.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Interactive storybook reading
N/A

Detailed Description

Children with Specific Language Impairment (SLI) are slower to learn new words than their peers, placing them at risk for academic failure. Our long-term goal is to develop an effective word learning treatment for kindergarten children with SLI, thereby improving their academic and vocational outcomes. During the prior funding period, we successfully taught new words to children with SLI via interactive book reading, a treatment involving an adult reading a storybook to a child and deviating from the text to teach new words. We identified the adequate intensity of the treatment and showed that children with SLI learn an appropriate number of words by the end of 8-weeks of treatment, approximating the number of words learned by typically developing children in prior studies. However, this successful support of short-term word learning revealed new challenges that must be overcome in this renewal to continue to understand and improve long-term word learning by children with SLI. Thus, a second preliminary clinical trial involving 60 kindergarten children with SLI is proposed. Aim 1 addresses the challenge that newly learned words were forgotten once treatment was withdrawn. We attempt to buffer forgetting by comparing different amounts of testing during interactive book reading (low vs. mid vs high testing). Incorporating testing into training is a well-established and highly replicated means of reducing forgetting by adults and typically developing children. Aim 1 will determine whether testing can be harnessed to buffer forgetting by children with SLI under real world conditions. Aims 2 and 3 address the challenge that not all children benefitted equally from interactive book reading. In Aim 2, we identify pre-treatment characteristics of children with SLI that are associated with the slope of learning during treatment or the slope of forgetting post-treatment. Moreover, we select a pre-treatment battery that samples a wide array of skills likely to be associated with learning (language processing, working memory, and episodic memory) or forgetting (overall learning during treatment, decay rate). Aim 2 will provide a foundation for predicting which children will benefit from interactive book reading and will identify which skills are major barriers to long-term word learning by children with SLI. In Aim 3, we classify each child's response at the end of treatment (learner vs. non-learner) and at the end of post-treatment monitoring (rememberer vs. forgetter). Then, we examine earlier performance to determine when treatment and post-treatment outcomes can be predicted. This yields empirically based benchmarks for progress that can be used to tailor the treatment to individual children and establishes the stability of learning and forgetting over time. Overall, this research advances a promising treatment to effectively overcome the significant word learning challenges faced by children with SLI and reveals the contribution of learning and forgetting to language normalization by children with SLI. The results will have impact beyond word learning and SLI because all treatments require boosting learning and buffering forgetting. Thus, the knowledge gained will further catalyze clinical research.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Children will be randomly assigned to one of three treatment armsChildren will be randomly assigned to one of three treatment arms
Masking:
Single (Outcomes Assessor)
Masking Description:
Pre- and post-outcome assessments will be performed by an individual blind to arm assignment.
Primary Purpose:
Treatment
Official Title:
Interactive Book Reading to Accelerate Word Learning by Children With SLI
Actual Study Start Date :
Jul 2, 2018
Anticipated Primary Completion Date :
May 1, 2024
Anticipated Study Completion Date :
May 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Low Testing

Children will receive 0 testing (talking) exposures and 6 listening exposures for a total of 6 exposures to each word. This is a listening only condition with minimal testing.

Behavioral: Interactive storybook reading
Children will be taught 30 words prior to, during, and after reading a commercially available storybook by an adult.
Other Names:
  • interactive book reading
  • dialogic reading
  • Experimental: Mid Testing

    Children will receive 2 testing (talking) exposures and 4 listening exposures for a total of 6 exposures to each word. This is a listening and talking condition with mostly listening.

    Behavioral: Interactive storybook reading
    Children will be taught 30 words prior to, during, and after reading a commercially available storybook by an adult.
    Other Names:
  • interactive book reading
  • dialogic reading
  • Experimental: High Testing

    Children will receive 4 testing (talking) exposures and 2 listening exposures for a total of 6 exposures to each word. This is a listening and talking condition with mostly talking.

    Behavioral: Interactive storybook reading
    Children will be taught 30 words prior to, during, and after reading a commercially available storybook by an adult.
    Other Names:
  • interactive book reading
  • dialogic reading
  • Outcome Measures

    Primary Outcome Measures

    1. Change in definition scores from pre- to 12-weeks post-treatment [20 weeks: pre-treatment, treatment (7.5 weeks), 12-weeks post-treatment]

      All new words will be presented. The child will be asked to provide a definition. Definitions will be scored as 0, 1, 2,or 3 points

    Secondary Outcome Measures

    1. Change in naming scores from pre- to 12-weeks post-treatment [20 weeks: pre-treatment, treatment (7.5 weeks), 12-weeks post-treatment]

      A picture and a prompt will be provided for each word and the child will be asked to name the word. Naming responses will be scored as 0 or 1 point

    Other Outcome Measures

    1. Change in untaught vocabulary [10 weeks: pre-treatment, treatment (7.5 weeks), immediate post-treatment]

      Pre-treatment general vocabulary measures will be re-administered post-treatment

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    5 Years to 6 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    Eligible for kindergarten enrollment Age 5-6 years Normal hearing Normal nonverbal IQ -- Nonverbal IQ of 85 or higher Language impairment as documented by language score </= 94 on SPELT-3 or </=91 on TNL-2 Vocabulary impairment as documented by a vocabulary score </= 6 on DELV, </= 6 on CELF-4 Word Classes, </= 6 on CCC-2

    Exclusion Criteria:

    Speaks more than one language Health history indicating neurologic or other disorder that would exclude a diagnosis of SLI (e.g., autism, developmental disability)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Kansas Lawrence Kansas United States 66045

    Sponsors and Collaborators

    • University of Kansas
    • National Institute on Deafness and Other Communication Disorders (NIDCD)

    Investigators

    • Principal Investigator: Holly Storkel, University of Kansas

    Study Documents (Full-Text)

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Kansas
    ClinicalTrials.gov Identifier:
    NCT03586479
    Other Study ID Numbers:
    • 20482
    • 2R01DC012824
    First Posted:
    Jul 13, 2018
    Last Update Posted:
    Apr 6, 2022
    Last Verified:
    Apr 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University of Kansas
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 6, 2022