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The purpose of this study is to establish a new Chinese children's speech and language norm by obtaining the latest data of speech and language development of children aged 2 ~ 6 from different regions in China. At the same time, the overall development level and group differences of speech and language in Chinese children aged 2 to 6 years, and the influencing factors of speech and language development in Chinese children aged 2 to 6 years were also discussed.
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Inclusion criteria
For normally developing children
All children must meet all of the following criteria simultaneously:
Informed consent of legal guardian or group representative;
Age from 2 to 6 years old, male and female;
Native speaker of Mandarin;
Children in kindergartens and hospitals are professionally assessed as normal development, which is defined as children without intellectual development disorder, developmental speech or language disorder, autism spectrum disorder, and attention deficit hyperactivity disorder.
For abnormally developed children
Informed consent of legal guardian or group representative;
Age from 2 to 6 years old, male and female;
Native speaker of Mandarin;
Children with intellectual development disorder, autism spectrum disorder and attention deficit hyperactivity disorder are assessed professionally in the hospital; Diagnostic criteria were referred to Diagnostic and Statistical Manual of Mental Disorders (DSM-5)
Exclusion criteria
For normally developing children
Poor coordination;
Other unsuitable children considered by researchers, such as children whose developmental level is basically normal but whose environmental and socio-economic factors (premature birth, low birth weight, malnutrition, abuse, etc.) have been verified to affect language development.
For abnormally developed children
Study the poor fit degree;
Have visual and hearing impairment;
Other unsuitable children considered by researchers, such as children with other organic dysfunction, such as cerebral palsy, congenital genetic diseases, epilepsy, etc.
5,744 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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