Completed

Characteristics of Idiopathic Familial Speech Disorders

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What is being collected

Data Collection

Who is being recruted

Communication Disorders+7

+ Language Disorders

+ Nervous System Diseases

See all eligibility criteria
How is the trial designed

Observational
Study Start: May 1996
See protocol details

Summary

Principal SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Last updated: July 2, 2017
Sourced from a government-validated database.Claim as a partner

Study start date: May 22, 1996

Actual date on which the first participant was enrolled.

Objective: Our objective is to determine which factors are involved in the development of stuttering and familial phonological processing disorder and are associated with a familial pattern of inheritance. Study population: The study population is comprised of 8 groups: Children and adults with persistent developmental stuttering; Unaffected siblings of the individuals affected with developmental stuttering or recovered from stuttering Children and adults who have recovered from developmental stuttering; Children and adults with persistent familial phonological processing disorders (FPPD); Unaffected siblings of the individuals affected with FPPD or have recovered from FPPD Children and adults who have recovered from FPPD; Unaffected siblings of the individuals who have recovered from FPPD; Children and adults with normal speech and language development who will comprise the control groups. Design: A Natural history design will be used to compare affected and unaffected family members with healthy volunteers with normal speech and language. Outcome Measures: Genetic markers and pedigree analyses will be used to test familial inheritance patterns. Speech and language development will be compared using indices of speech perception, auditory perception, self monitoring of one's own speech, language complexity, motor complexity, speech learning, phonological processing and verbal/nonverbal memory.

NCT00001551
Principal SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Last updated: July 2, 2017
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

375 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Communication DisordersLanguage DisordersNervous System DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsNeurobehavioral ManifestationsArticulation DisordersSpeech DisordersStuttering

Criteria

-INCLUSION CRITERIA: i. Normal Language Development, Hearing and Cognition ii. The following screening tests previously published with norms were found to have a good distribution for determining normal functioning in adolescents and adults as all subjects did not hit ceiling and all had scores greater than or equal to the 80th percentile. These tests are being used to ensure that subjects affected with stuttering or FPPD do not have other disorders such as hearing loss, language delay, or mental retardation. Peabody Picture Vocabulary Test III (PPVT-III) Expressive Vocabulary Test (EVT) Oral Speech Mechanism Screening Examination Revised Token Test; Token test for Children Test of Non verbal intelligence (TONI-2) Digit Span subtest of the WICS-R Audiometric Screening Goldman Fristoe Test of Articulation WUG Test of Morphological Encoding Test of Auditory Comprehension of Language (TACL) Khan-Lewis Phonological Analysis INCLUSION CRITERIA FOR IDENTIFYING AND QUANTIFYING STUTTERING: The Stuttering Severity Index -3 (Riley, 1981) has been found to be accurate for identifying and assessing the severity of stuttering during conversational speech. For the inclusion of a stuttering subject we require: i. A total overall score of 11 or greater between 3 and 17 years, ii. A total overall score of 18 or greater from age 18 and above. INCLUSION CRITERIA FOR IDENTIFYING FPPD: i. A family history of an autosomal dominant pattern of inheritance of the speech disorder over several generations with persistence into adulthood in some cases, ii. Speech symptoms during conversational speech include: deletion of final consonants; syllable reduction and syllable deletion; deletion of grammatical markers such as copulas, auxiliaries, prepositions, connectives; poor ability to self-correct; poor awareness of errors; and consonant cluster reduction. iii. Greater than 9% discourse errors during analysis of a sample of 300 syllables. iv. A discrepancy of 30 points (1 and 1/2 Standard Deviations) between receptive (the higher score) and expressive percentile score on the PPVT III and Expressive Vocabulary Test. v. For subjects greater than 7 years of age, a phonological process rating of 3 or more for any phonological process on the Khan-Lewis Phonological Analysis. For subjects less than 7 years of age, a phonological process rating of 3 or more on 2 phonological processes on the Khan-Lewis Phonological Analysis. Finally, any subjects with a non developmental phonological process error will be identified as potentially having FPPD. EXCLUSION CRITERIA: i. Anyone with a hearing loss will be excluded from participation during the diagnostic testing. ii. Children with delayed language, more than 1 year delay from norms on receptive and expression language testing will be excluded. iii. Language impairment: scores more than 2 standard deviations below the age appropriate score on the standardized language tests listed under the inclusion criteria. iv. Cognitive impairment: scores more than 2 standard deviations below the age appropriate score on the standardized cognitive tests listed under the inclusion criteria. v. Bilingual non-native English speakers - Studies have demonstrated that brain organization for speech and language may differ in bilingual persons. It is hypothesized that this may alter speech motor learning and thus kinematic data from non-native English speakers would differ from native English speakers. Therefore, only native-American English speakers, with only one language spoken in the home, will be included.

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 2 locations

University of Maryland, College Park

College Park, United StatesOpen University of Maryland, College Park in Google Maps

University of Wisconsin

Madison, United States
Completed2 Study Centers