Genetics, Brain Structure and Thinking Skills in Autism
NCT01451983 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 138
Last updated 2015-01-14
Summary
The purpose of this research is to better understand the genetic, biochemical, cognitive and behavioral symptom abnormalities that contribute to autism spectrum disorders. The investigators anticipate recruiting at least 100 participants with autism spectrum disorder and large head size, at least 100 participants with autism spectrum disorder without large head size and at least 40 healthy siblings. Biological parents are expected to be recruited only as genetic changes are identified in individuals with autism spectrum disorders to better understand the nature of these genetic changes. Participants are asked to complete cognitive testing, a blood draw, urine collection and measurement of his/her height, weight and head circumference. Parents or caregivers may be asked to complete a diagnostic evaluation and will complete questionnaires that examine the participant's medical and family history as well as his/her current symptoms, functioning, and quality of life. A brief report simply listing and giving a basic description of any behavioral diagnostic information, autism symptoms, adaptive functioning, and a listing of results from cognitive testing will be provided as part of this study.
Conditions
- Autism Spectrum Disorders
Sponsors & Collaborators
-
National Institutes of Health (NIH)
collaborator NIH -
National Center for Research Resources (NCRR)
collaborator NIH -
The Cleveland Clinic
lead OTHER
Principal Investigators
-
Thomas W Frazier, Ph.D. · The Cleveland Clinic
-
Charis Eng, M.D., Ph.D. · The Cleveland Clinic
Eligibility
- Min Age
- 2 Years
- Max Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2010-05-31
- Primary Completion
- 2014-08-31
- Completion
- 2014-08-31
Countries
- United States
Study Locations
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