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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04658043
Other study ID # EA1811014
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 22, 2019
Est. completion date August 31, 2022

Study information

Verified date December 2020
Source The University of Hong Kong
Contact Terry Kit-fong Au
Phone (852) 2219 4776
Email terryau@hku.hk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to develop a culturally-sensitive parent-training intervention to enhance socioemotional functioning of young children (aged 3-6) with Autism Spectrum Disorder (ASD) in Mainland China. The investigators will conduct randomized controlled trials to evaluate the effectiveness and feasibility of this program in a pilot study and then a large-scale community-based study in Shenzhen, China, to examine the generalizability of the treatment outcomes of this intervention for Chinese children with ASD.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date August 31, 2022
Est. primary completion date August 31, 2022
Accepts healthy volunteers No
Gender All
Age group 3 Years to 6 Years
Eligibility Inclusion Criteria: - Children aged 3-6 - Living in Shenzhen, Mainland China - Diagnosed with ASD or suspected of having ASD

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Intervention on socioemotional functioning
A culturally sensitive intervention based on the "train the trainer (or coach the coach) model" for enhancing the social adaptive functioning of young children (aged 3-6) with ASD in China, via providing training for parents

Locations

Country Name City State
China Shenzhen University Shenzhen
Hong Kong University of Hong Kong Hong Kong

Sponsors (3)

Lead Sponsor Collaborator
The University of Hong Kong Guangdong Province, Department of Science and Technology, Shenzhen University

Countries where clinical trial is conducted

China,  Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Autism Diagnostic Observation Schedule, Second Edition (ADOS-2) ADOS-2 is a diagnostic measure used in this study to assess the change in children's ASD symptoms pre-intervention and 4-month post-intervention
Primary Change in the Autism Spectrum Quotient (AQ) AQ is a parent-report measure used in this study to measure change in children's ASD symptoms pre-intervention, immediately after the intervention, and 4-month post-intervention
Primary Change in Dyadic Parent-Child Interaction Coding System (DPICS system) The DPICS system is used in this study to measure the change in the quality of parent-child interaction through observations of dyads during free and structured play in the clinical setting and 5-minute parents' description of their children. The code categories include the number of command, praise, joint attention and verbal responsiveness, words used by parents and the intonation in their language. pre-intervention, immediately after the intervention, and 4-month post-intervention
Secondary Change in Parenting Stress Index, Fourth Edition Short Form (PSI-4-SF) PSI-4-SF is a parent-report measure used in this study to measure change in parenting stress pre-intervention, immediately after the intervention, and 4-month post-intervention
Secondary Change in Self-Efficacy in Nurturing Role Questionnaire Self-Efficacy in Nurturing Role Questionnaire is a parent-report measure used in this study to measure change in parents' self-efficacy pre-intervention, immediately after the intervention, and 4-month post-intervention
Secondary Change in Classroom Observation Scale (COS) COS is a teacher-report measure used in this study to measure children's social behaviours in classroom setting pre-intervention, immediately after the intervention, and 4-month post-intervention
Secondary Change in Social Responsiveness Scale, Second Edition (SRS-2) SRS-2 is a teacher-report measure used in this study to measure children's social behaviours pre-intervention, immediately after the intervention, and 4-month post-intervention
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