Symbolic Representation in Young Children With Down Syndrome
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Purpose
The aim of this study is to characterize the process of constitution of symbolic representation in infants with Down syndrome, as well as to investigate the relationship between gestures and the emergence of oral language. The investigators hypothesis is that children with Down syndrome could present difficulties during the constitution of symbolic representation that may be related to later deficits on expressive language, generally observed in these children.
| Condition |
|---|
|
Down Syndrome |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Prospective |
| Official Title: | The Constitution of Symbolic Representation in Young Children With Down Syndrome |
- Performance on monthly assessments administered after the initial evaluation [ Time Frame: 12 months ] [ Designated as safety issue: No ]
| Enrollment: | 25 |
| Study Start Date: | July 2006 |
| Study Completion Date: | April 2009 |
| Primary Completion Date: | April 2009 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
|
Study group
20 infants with Down syndrome
|
|
Control Group
15 typically developing children
|
Detailed Description:
According to the Genetic Epistemology, language development is directly related to cognitive construction. Such relationship is clearly observed after the constitution of representation that allows one individual to express his or her thinking through language.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Study Group - children with Down syndrome that attend speech-language therapy at the Speech Language Pathology Laboratory in Syndromes and Sensorimotor Deficits of the School of Medicine of the University of São Paulo or from the Association of Parents and Friends of Exceptional children of São José dos Campos.
Control Group
- typically developing children followed up in the Pediatrics Ambulatory of the University's Hospital and/or being assisted in the University' Hospital Nursery School.
Inclusion Criteria for Study Group:
- genetic diagnosis of Down Syndrome
- be at the 4th stage of sensorimotor period at the initial assessment
- good health conditions
- good results on audiologic evaluation
- pediatric and ear, nose and throat periodic check ups.
Inclusion Criteria for Control Group:
- good health conditions
- be at the 4th stage of sensorimotor period at the initial assessment
- pediatric and ear, nose and throat periodic check ups.
Exclusion Criteria for all groups:
- submission to long term hospitalizations due to heart diseases and major respiratory airway infections, that may interfere in the child's global development
- presence of visual or auditory important deficits
- historic of prematurely and/or low birth weight
Contacts and Locations| Brazil | |
| APAE Sao José dos Campos | |
| Sao Jose Dos Campos, Sao Paulo, Brazil, 12233-400 | |
| University Hospital | |
| Sao Paulo, São Paulo, Brazil, 05360-160 | |
| University of Sao Paulo - School of Medicine - Department of Physiotherapy, Communication Sciences and Disorders, Occupational Therapy | |
| Sao Paulo, Brazil, 05360-160 | |
| Study Chair: | Suelly CO Limongi, PhD. | University of Sao Paulo |
| Principal Investigator: | Fabiola C Flabiano, PhD. student | University of Sao Paulo |
More Information
No publications provided
| Responsible Party: | Suelly Cecilia Olivan Limongi, University of Sao Paulo |
| ClinicalTrials.gov Identifier: | NCT00668980 History of Changes |
| Other Study ID Numbers: | 06/50842-4 |
| Study First Received: | April 25, 2008 |
| Last Updated: | January 13, 2010 |
| Health Authority: | Brazil: National Committee of Ethics in Research |
Keywords provided by University of Sao Paulo:
|
Down syndrome symbolic representation gestures expressive language development |
Additional relevant MeSH terms:
|
Down Syndrome Mental Retardation Neurobehavioral Manifestations Neurologic Manifestations Nervous System Diseases |
Abnormalities, Multiple Congenital Abnormalities Chromosome Disorders Genetic Diseases, Inborn |
ClinicalTrials.gov processed this record on May 23, 2013