Stanford, California 94305

  • Developmental Disabilities

Purpose:

The investigators will assess the efficacy of parent delivered interventions in the treatment of social and communication deficits in children with autism. By collecting information about parent and child functioning before and after intervention, the investigators will be able to determine whether the intervention is effective in improving child social communication and reducing parent stress.


Criteria:

Inclusion Criteria for autism participants: - Children between the ages of 1.6 and 17.11 years of age - Males and females - Diagnosis of autism based on DSM-IV-TR criteria, an expert clinical evaluation, and ADOS or ADI-R if needed - Receiving or will receive a parent delivered intervention to alleviate symptoms related to their diagnosis of autistic disorder - Have a care provider that will reliably bring subjects to their chosen intervention and clinic visits, and is trustworthy to provide accurate accounts of services provided to the subject Inclusion Criteria for developmentally delayed participants: - Will have an age range between 1.6 and 17.11 years of age - Males or females - Diagnosis of a developmental delay or disorder based on DSM-IV-TR, ICD-10, and an expert clinical evaluation - Have historical evidence of significant abnormal developmental milestones as determined by neurological history - Receiving or will receive a parent delivered intervention - Have a care provider that will reliably bring subjects to their chosen intervention and clinic visits, and is trustworthy to provide accurate accounts of services provided to the subject Exclusion Criteria for autism participants: - Is medically unstable (e.g., more than one seizure a month) - Have a medical diagnosis that causes autism like symptomology (e.g., Fragile X, Down syndrome, Angelman's syndrome, tuberous sclerosis, Rett's disorder) Exclusion Criteria for developmentally delayed subjects: - Is medically unstable (e.g., more than one seizure a month) - Has a diagnosis of ASD


NCT ID:

NCT01882153


Primary Contact:

Principal Investigator
Antonio Y Hardan, M.D.
Stanford University

Estefania Millan
Phone: 650-736-1235
Email: mmillan2@stanford.edu


Backup Contact:

Email: rlibove@stanford.edu
Robin Libove
Phone: 650-736-1235


Location Contact:

Stanford, California 94305
United States

Robin Libove, BS
Phone: 650-736-1235
Email: rlibove@stanford.edu

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: September 16, 2021

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