Defining the Brain Phenotype of Children With Williams Syndrome
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|ClinicalTrials.gov Identifier: NCT01132885|
Recruitment Status : Recruiting
First Posted : May 28, 2010
Last Update Posted : June 15, 2021
- Little is known about how the brain changes during childhood and adolescence, how genes affect this process, or how the brains of people with Williams syndrome change during this period. Genetic features of Williams syndrome affect the brain s development, but the details of this process have not been studied over time. Researchers are interested in using magnetic resonance imaging to study how the brain changes in healthy children and children with Williams syndrome and related genetic disorders.
- To study developmental changes in the brains of healthy children and children who have been diagnosed with Williams syndrome or a related genetic disorder.
- Healthy children and adolescents between 5 and 17 years of age.
- Children and adolescents between 5 and 17 years of age who have been diagnosed with Williams syndrome or genetic characteristics that overlap with Williams syndrome.
- Participants will have a brief physical examination and tests of memory, attention, concentration, and thinking. Parents will be asked about their child s personality, behavior characteristics, and social interaction and communication skills.
- Both participants and their parents may be asked to complete additional questionnaires or take various tests as required for the study.
- Participants will have approximately 10 hours of magnetic resonance imaging (MRI) scanning, usually over 4 to 5 days, within a one month period. Some of these tests will require the participants to do specific tasks while inside the MRI scanner.
- Participants will be asked to return to the National Institutes of Health clinical center to repeat these procedures every 2 years thereafter until age 18.
|Condition or disease|
|Study Type :||Observational|
|Estimated Enrollment :||415 participants|
|Official Title:||Defining the Brain Phenotype of Children With Williams Syndrome|
|Actual Study Start Date :||January 23, 2011|
Adults with WS or genetic abnormalities
Adults with Williams syndrome or genetic abnormalities in chromosome 7q11.23
Children with WS or genetic abnormalities
children ages 5 17 with Williams Syndrome or genetic abnormalities in chromosome 7q11. 23
Parents of children with 7q11.23 CNV will undergo blood draws
Siblings of children with 7q11.23 CNV
Typically developing children ages ages 5 -17
- fMRI Task Procedures [ Time Frame: Ongoing ]fMRI Task Procedures
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01132885
|Contact: Jasmin Czarapata, Ph.D.||(301) email@example.com|
|Contact: Karen F Berman, M.D.||(301) firstname.lastname@example.org|
|United States, Maryland|
|National Institutes of Health Clinical Center, 9000 Rockville Pike||Recruiting|
|Bethesda, Maryland, United States, 20892|
|Contact: For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR) 800-411-1222 ext TTY8664111010 email@example.com|
|Principal Investigator:||Karen F Berman, M.D.||National Institute of Mental Health (NIMH)|