A Comparison of Language Intervention Programs

Sponsor
National Institute on Deafness and Other Communication Disorders (NIDCD) (NIH)
Overall Status
Completed
CT.gov ID
NCT00033150
Collaborator
(none)
216
2
31
108
3.5

Study Details

Study Description

Brief Summary

Brief Summary:

Nearly 7% of elementary school children present with difficulties learning and using language. Unfortunately, language impairments are often long lasting and may have serious social, academic, and vocational ramifications. More than 1 million children receive language intervention in the public schools each year, and many more are seen in hospitals and other clinical settings.

This randomized clinical trial compares the language outcomes of Fast ForWord to two other interventions (computer assisted language intervention without acoustically modified speech and individual language intervention) and to the outcomes of an academic enrichment (control) condition. Each year for 3 years, children will be randomly assigned to each of the four conditions at three regional sites (Austin, Texas, Dallas, Texas, and Lawrence, Kansas). The treatments will be administered in special summer programs. The primary research question is which intervention results in the most improvement in the composite language score from the Oral and Written Language Scales. Secondary questions include which intervention results in the greatest gains in conversational language,which intervention results in the greatest gains 3 and 6 months after training, which intervention results in the greatest improvement in auditory perception, and which intervention is the most cost effective.

The results of the study will have theoretical and practical value. Theoretically, the study tests the temporal processing hypothesis of language impairment. Practically, the study will describe and compare the language, communication, auditory processing and academic outcomes of different language interventions. The study will help clinicians and administrators choose the most effective and least expensive treatment for the children they serve.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Fast ForWord
  • Behavioral: Computer Assisted Language Intervention
  • Behavioral: Individual Language Intervention
  • Behavioral: Academic enrichment
Phase 3

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single
Primary Purpose:
Treatment
Official Title:
A Comparison of Language Intervention Programs
Study Start Date :
Jun 1, 2002
Study Completion Date :
Jan 1, 2005

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    6 Years to 9 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • age 6 to 9 years

    • score between 75 and 125 on the Matrices subtest of the Kaufman Brief Intelligence Test

    • Speaking Quotient of 79 or lower on the Test of Language Development: Primary: 3rd Edition

    Exclusion Criteria:
    • Previous participation in 8 or more hours of language intervention or classroom activities using any of the Fast ForWord, Laureate, or Earobics speech-language or reading software and/or the Lindamood-Bell auditory discrimination training

    • Failure of a hearing screening test

    • An episode of otitis media in the previous 12 months

    • Evidence of focal brain lesion, traumatic brain injury, cerebral palsy, or seizure disorder

    • Abnormality of oral structure or function impeding normal language production

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Lawrence Public Schools USD 497 Lawrence Kansas United States 66044
    2 Pflugerville Independent School District Pflugerville Texas United States 78660

    Sponsors and Collaborators

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

    Investigators

    • Principal Investigator: Ronald Gillam, PhD, Pflugerville Independent School District

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00033150
    Other Study ID Numbers:
    • U01DC004560
    First Posted:
    Apr 9, 2002
    Last Update Posted:
    Apr 24, 2006
    Last Verified:
    Apr 1, 2006
    Keywords provided by , ,
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 24, 2006