Autism Clinical Trial
Official title:
Effectiveness of Joint Attention Intervention in Young Children With Autism - a Randomized Study
The purpose of this study is to investigate the effectiveness of an intervention aimed to increase joint attention in 2-4 year old children with autism. The study will be conducted in mainstream preschools in Norway. The intervention will be implemented by preschool teachers and paraprofessionals supervised by trained counselors.
Young children with autism experience severe deficit in joint attention skills (e.g.
pointing to objects, showing, following another person's gaze, responding to invitations to
social interaction). Ability to initiate and respond to joint attention is linked to
children's later language abilities. As a mean to improve language outcome in children with
autism, it is important to target joint attention in early intervention programs.
This study investigates the effectiveness of a joint attention intervention. Sixty 2-4 year
old children with autism will be randomized to an intervention group or a control group.
Children in both groups will continue their ordinary preschool program. However, the
children in the intervention group will also participate in 80 joint attention intervention
sessions. The sessions (20 minutes each) will be conducted twice a day for 8 weeks by
preschool teachers or paraprofessionals working in the preschools. Before starting the
intervention preschool teachers and paraprofessionals will be taught how to teach joint
attention skills and how to initiate and maintain episodes of joint engagement. During the
course of intervention they will be supervised by trained counselors.
Outcome measures will include joint attention skills, language skills and joint engagement.
Children will be assessed at baseline, after 10 weeks and at follow up 6 months and 1 year
after the end of the intervention. The measures are based on direct testing of the children,
video observations and questionnaires to parent and professionals.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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