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Speech Therapy for Down Syndrome
N/A
Recruiting
Led By Stephen Camarata, PhD
Research Sponsored by Vanderbilt University Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Previous medical identification of Down Syndrome
Chronological age 6-14 years
Timeline
Screening 3 weeks
Treatment Varies
Follow Up six months
Awards & highlights
Study Summary
This trial is measuring speech-articulation accuracy and speech intelligibility in children with Down Syndrome to see if a treatment can help improve speech intelligibility.
Who is the study for?
This trial is for children with Down Syndrome aged 6 to 14 who can use at least three-word sentences, as reported by parents. They must pass a hearing test and have no history of seizures, ADHD, apraxia due to neurological disorders, stuttering, autism (as measured by specific diagnostic scales), or severe disruptive behavior.Check my eligibility
What is being tested?
The study tests the effectiveness of a speech therapy called 'Lexically based speech recast' in improving the clarity of speech in children with Down Syndrome. It will assess how well they articulate words and understand vocabulary before and after treatment.See study design
What are the potential side effects?
Since this intervention involves speech therapy techniques without medication or surgery, there are no direct physical side effects expected from participating in this trial.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have been diagnosed with Down Syndrome.
Select...
I am between 6 and 14 years old.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ six months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~six months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Speech Accuracy
Speech Intelligibility
Secondary outcome measures
Speech Rate
Trial Design
1Treatment groups
Experimental Treatment
Group I: Lexically Based Speech Intelligibility RecastExperimental Treatment1 Intervention
Speech recasts are likely to improve speech intelligibility in Down Syndrome. The goal of this study is to induce change in speech intelligibility in order to study phonological, acoustic and suprasegmental sequelae of improvements in speech.
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Who is running the clinical trial?
Vanderbilt University Medical CenterLead Sponsor
865 Previous Clinical Trials
673,133 Total Patients Enrolled
National Institute on Deafness and Other Communication Disorders (NIDCD)NIH
331 Previous Clinical Trials
178,467 Total Patients Enrolled
Stephen Camarata, PhDPrincipal InvestigatorVUMC Dept of Hearing & Speech Sciences
1 Previous Clinical Trials
72 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I have been diagnosed with Down Syndrome.You have a history of seizures, or your parents have reported that you had seizures.I have difficulty with movements because of a brain disorder.You have been diagnosed with ADHD.You need to pass a hearing test when you join the project.You have been diagnosed with Autism Spectrum Disorder based on specific test scores.I am between 6 and 14 years old.You have behavior that would make it hard for you to take part in testing or treatment.People who have difficulty speaking fluently.You speak using short sentences of three words or less, as reported by your parent and confirmed during evaluations.
Research Study Groups:
This trial has the following groups:- Group 1: Lexically Based Speech Intelligibility Recast
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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