- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04059354
Down Syndrome Speech Intelligibility Diagnostic Treatment Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This Down Syndrome (DS) speech intelligibility diagnostic treatment study is a pilot clinical intervention study assessing the efficacy of an integrative speech treatment approach for individuals with DS. DS is a common genetic disorder that causes lifelong intellectual disability where speech intelligibility is typically compromised affecting quality of life. The clinical management of communication disorders in individuals with DS is a priority for NIH's National Institute on Deafness and Other Communicative Disorder. The proposed treatment addresses the void in speech intervention and is based on our Vocal Tract Development Laboratory's (VTLab) research findings on anatomic, acoustic and perceptual studies from speakers with DS. Having identified specific difficulties in the production and perception of select vowels, this treatment focuses on accurate vowel production, while combining and adapting two established speech treatment approaches on articulatory accuracy and motor learning. The articulatory treatment uses the cycles phonological approach and the motor learning treatment is script training.
Findings from this clinical intervention study are expected to pave the path towards optimal management of speech intelligibility in speakers with DS. The current pilot study is open to males based on findings from our lab's research that males are less intelligible than their female peers. The investigators also expect findings to provide the preliminary data needed to bridge the gap towards an exploratory clinical research proposal on functional anatomy as an intervention strategy for both males and females.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Wisconsin
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Madison, Wisconsin, United States, 53705
- Waisman Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Males with a diagnosis of Down syndrome between the ages of 7 and 16 years
- Primary language is English
- Interested in improving their speech intelligibility.
- All participants must consent/assent to participate. As this is a multiple single subject design, services are available to all motivated participants who are willing to commit to the time/durations described in the diagnostic treatment.
Exclusion Criteria:
- Primary language is not American English
- Do not have a diagnosis of Down syndrome
- Female
- Ages birth-6 and 17 years or older
- Individuals who have a co-occurring diagnosis that affects communication abilities [e.g., diagnosed as deaf with cochlear implants, Autism, only use an alternative/augmentative communication (AAC) device to communicate],
Severe hearing loss which will limit their ability to participate in the treatment
- Individuals with a known mild or moderate hearing loss or current speech- language therapy services will not be excluded, but this information will be requested in the Parent Questionnaire. In addition, access to their current individualized education program (IEP) will be requested.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Speech therapy
Direct speech therapy will be provided for a 12 week period with up to three one-hour sessions per week.
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Determine the efficacy of a newly devised intensive speech treatment plan (DS-DxTx) focusing on vowels that combines efficacious treatment approaches to use with individuals with Down syndrome.
The phonological speech intervention, Phonological Cycles approach, is designed for use with children with highly unintelligible speech and the speech motor learning intervention, Script training is a functional treatment to promote phrase level productions.
Both approaches are documented to be efficacious with other speech disorders.
The proposed approach takes into account the multiple deficits commonly present in individuals with DS, and based on the acoustic and perceptual finding on vowels from our VTLab.
Acoustic and perceptual measures will be used to assess treatment efficacy.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in formant frequency for vowels in recorded words/sentences.
Time Frame: Baseline, 3 months, 4 months, and 9 months.
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The participant's vowels in recorded words/sentences will be subjected to acoustic analysis to assess changes in measures of the fundamental frequency (F0) and formant frequencies F1, F2, F3, and F4 (first four resonant frequencies of the vocal tract).
All measurements will be made in Hertz (Hz).
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Baseline, 3 months, 4 months, and 9 months.
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Change in formant bandwidth for vowels in recorded words/sentences.
Time Frame: Baseline, 3 months, 4 months, and 9 months.
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The participant's vowels in recorded words/sentences will be analyzed acoustically to measure the formant bandwidth (or thickness of the resonant frequencies).
Much like formants, the measurement unit for formant bandwidth is in Hertz (Hz) .
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Baseline, 3 months, 4 months, and 9 months.
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Change in time to produce the individual phonemes in recorded words/sentences will be measured.
Time Frame: Baseline, 3 months, 4 months, and 9 months.
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The participant's duration measurements for phonemes (vowels, consonants) produced and the time taken to produce an entire word will be measured in recorded words .
For example, the word "hat" the sounds "h", "a", and "t" would all be measured for their durations, along with the time it takes to produce the sounds in the entire word "hat'.
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Baseline, 3 months, 4 months, and 9 months.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Hodson Assessment of Phonological Patterns-3 (HAPP-3) score.
Time Frame: Baseline, 3 months, 4 months, and 9 months.
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The Hodson Assessment of Phonological Patterns-Third Edition (HAPP-3) is a valid, reliable, standardized test that is norm-referenced and also criterion-referenced.
The HAPP-3 was designed for children with highly unintelligible speech.
The reported score will be a sum of word/syllable omissions score plus the consonant category deficiencies score.
Severity scores are a range, score 1-50 is rated mild, 51-100 is moderate, 101-150 is severe, and >150 is profound.
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Baseline, 3 months, 4 months, and 9 months.
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Change in Peabody Picture Vocabulary Test-4 (PPVT-4) score.
Time Frame: Baseline, 3 months, 4 months, and 9 months.
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Peabody Picture Vocabulary Test-4 (PPVT-4) is an assessment measure of receptive vocabulary for Standard English.
Higher scores suggest greater vocabulary knowledge.
Standard scores are rated 20-150.
20-69 are Extremely low score, 70-84 Moderately low score, 85-114 Average score, 115-129 Moderately high score, and 130-160 Extremely high score.
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Baseline, 3 months, 4 months, and 9 months.
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Change in the percentage of correct phonemes derived from a language sample
Time Frame: Baseline, 3 months, 4 months, and 9 months.
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A language sample will be recorded and analyzed at baseline and post- treatments.
The percentage of phonemes (a phoneme is any of the perceptually distinct units of sound in a specified language that distinguish one word from another, it will include both vowels and consonants) will be derived from these participant's recordings as a rating of intelligibility.
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Baseline, 3 months, 4 months, and 9 months.
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Percentage of correct consonants in recorded words/sentences rated by perceptual listeners
Time Frame: Baseline, 3 months, 4 months, and 9 months.
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Adult listeners will listen to and rate the participant's recorded words/sentences by typing what they hear.
A percentage of correct consonants is measured by comparing the stimuli and the perceptual raters outcome.
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Baseline, 3 months, 4 months, and 9 months.
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Percentage of correct vowels in recorded words/sentences rated by perceptual listeners
Time Frame: Baseline, 3 months, 4 months, and 9 months.
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Adult listeners will listen to and rate the participant's recorded words/sentences by typing what they hear.
A percentage of correct vowels is measured by comparing the stimuli and the perceptual raters outcome.
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Baseline, 3 months, 4 months, and 9 months.
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Change in scores for the Intelligibility in Context Scale
Time Frame: Baseline, 3 months, 4 months, and 9 months.
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The Intelligibility in Context Scale is a quick parent reported measure of children's intelligibility.
The 7-item questionnaire rates the degree to which children's speech is understood by different communication partners (parents, immediate family, extended family, friends, acquaintances, teachers, and strangers) on a 5-point scale.
The score ranges from 7-35, higher scores correlate with higher intelligibility.
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Baseline, 3 months, 4 months, and 9 months.
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Change in number of correct words/sentences produced in the Scripts
Time Frame: Baseline, 3 months, 4 months, and 9 months.
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The participant's will learn basic Scripts on common communication topics of their choice (ordering in a restaurant, favorite movie, inviting a friend over).
The percentage of words correct in the script is measured by counting the correct words produced intelligibly out of the total words.
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Baseline, 3 months, 4 months, and 9 months.
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Houri K Vorperian, PhD, University of Wisconsin, Madison- Waisman Center
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019-0706
- A348700 (Other Identifier: UW Madison)
- VCRGE/WAISMAN/WAISMAN (Other Identifier: UW Madison)
- Protocol Version 12/10/2019 (Other Identifier: UW Madison)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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