Full Text View
Tabular View
No Study Results Posted
Related Studies
Hereditary Deficits in Auditory Processing Leading to Language Impairment
This study is currently recruiting participants.
Study NCT00004570   Information provided by National Institutes of Health Clinical Center (CC)
First Received: February 14, 2000   Last Updated: August 24, 2009   History of Changes

February 14, 2000
August 24, 2009
February 2000
October 2003   (final data collection date for primary outcome measure)
 
 
Complete list of historical versions of study NCT00004570 on ClinicalTrials.gov Archive Site
 
 
 
Hereditary Deficits in Auditory Processing Leading to Language Impairment
Identification of Hereditary Auditory Temporal Processing Deficits

Some children with certain language disorders may not properly process the sounds they hear, resulting in language impairments. The purpose of this study is to determine if deficits in auditory temporal processing-the way the brain analyzes the timing and patterns of sounds-are an inherited trait.

Families with auditory temporal processing deficits are sought in order to identify the genes responsible for auditory temporal processing deficits. Children and adults with a diagnosis or history of language impairment in the family and their family members-both affected and non-affected-are eligible for this two-part study. In Part 1, participants undergo a series of language tests and listening tests to measure various characteristics of how they perceive sound. In Part 2, they are interviewed about language disorders, learning disabilities, and other medical problems of family members. This information is used to construct a pedigree (family tree diagram) showing the pattern of inheritance of family traits. Study subjects whose pedigree indicates that language disorders may be hereditary in their family will provide either a small blood sample (1 to 2 tablespoons) or a tissue specimen obtained from a cheek swab (rubbing the inside of the cheek with a small brush or cotton swabs). The sample will be used to isolate DNA for genetic analysis.

Recent research implicates auditory processing deficits in the etiology of language impairments, but no standard methodology has been employed to determine whether auditory processing deficits are heritable traits. We are presently evaluating a battery of auditory processing measures in twins recruited from the general population. Our data indicates that performance on some of these tests has a significantly heritable component. We seek IRB approval to recruit these research subjects and their families into genetic studies to investigate the heritability of auditory temporal processing characteristics, and identify the causative genes.

 
Observational
 
  • Auditory Perceptual Disorder
  • Language Delay
  • Language Disorder
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
800
 
October 2003   (final data collection date for primary outcome measure)
  • INCLUSION CRITERIA:

Diagnosis of auditory processing disorder (APD/CAPD) based on two or more standardized tests of auditory processing.

Age 6 to 85 years.

EXCLUSION CRITERIA:

Hearing loss with onset prior to age 20 years, defined as:

  • Air conduction pure tone thresholds (250-8000 Hz) exceeding 20 dBHL
  • Air-bone gaps, even in the presence of normal sensitivity, exceeding 10 dBHL
  • Abnormal tympanogram

History of chronic/recurrent otitis media

History of ear surgery

History or diagnosis of central nervous system lesions/pathology, including:

  • Intracranial tumors
  • Cerebrovascular disease
  • Degenerative CNS disorders
  • CNS trauma
  • Encephalitis
  • Meningitis

Currently on medications capable of altering CNS function

History of treatment with ototoxic medication

History or diagnosis of:

  • Attention deficit hyperactivity disorder (ADHD)
  • Attention deficit disorder (ADD)

Non-English Speaking

English as a second language

Diagnosis of auditory neuropathy

Both
6 Years to 85 Years
Yes
Contact: Patient Recruitment and Public Liaison Office (800) 411-1222 prpl@mail.cc.nih.gov
Contact: TTY 1-866-411-1010
United States
 
NCT00004570
 
000073, 00-DC-0073
National Institute on Deafness and Other Communication Disorders (NIDCD)
 
 
National Institutes of Health Clinical Center (CC)
January 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP