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Clinical Trials/NCT03254264
NCT03254264
Terminated
N/A

Impact of Early Intervention on Neurocognitive Profile of Children With Autism Spectrum Disorder

Hôpital le Vinatier1 site in 1 country1 target enrollmentMay 29, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Autism Spectrum Disorder
Sponsor
Hôpital le Vinatier
Enrollment
1
Locations
1
Primary Endpoint
The primary outcome will be the time spent on biological motion in the task of visual preference stimuli.
Status
Terminated
Last Updated
4 years ago

Overview

Brief Summary

The Early start Denver model (Rogers, 2010; Dawson, 2010) is a developmental and behavioral model that aim to enhance socio-comunicative abilities and also global development of children with Autism spectrum disorder (ASD). The purpose of this study is to identify changes in neurocognitive profile of children population with ASD receiving Early Start Denver Model (ESDM) applied 12 hours per week in comparison to children receiving other interventions. That is a study proposed to children with ASD and their families that participate already to a randomized control study called IDEA registered on clinicaltrials.gov NCT02608333.

the investigators hypothesized that ESDM would increase social cognition, reduce shifting attention time and increase preference for unpredictable stimuli.

Detailed Description

IDEA is a multicenter (4 centers in France and 1 center in Belgium), randomized, controlled, single blind trial using a modified Zelen design .It concerns children with ASD aged 15 to 36 months without severe neurological or physical disorder and living in the proximity of one the early intervention units. After diagnostic, Children will be included in a longitudinal cohort with the consent of the parents. Sixty children will be drawn lots among 180 children of the cohort and will be included in an ESDM intervention with the consent of the parents. Two groups will be compared: an experimental group of 60 children receiving 12 hours a week of ESDM intervention delivered by trained therapists during 2 years and a control group of 120 children receiving typical heterogeneous 'as-usual' intervention proposed by professionals and public services over the same period. In IDEA development of communication and social interactions and global developmental of all the children will be measured at different time points (at baseline (t0), after 1 year (t1), after 2 years( t2)) over the two years through standardized tests such as Autism diagnostic observation Schedule (ADOS-2), Mullen Scales of Early Learning (MSEL) and the Vineland Adaptive Behavior Scale (VABS-2). Children will be included in this second study called IDEA-EYE with parents' consent. Then, preference for biological motion and social scene, shifting attention time and preference for sameness will be measure in both groups with an Eye-tracker Tobii TX 300 at t0,t1 and t2. These measures will also be collected in a group of children without ASD at t0,t1 and t2. the investigators expect, as primary criteria, a significant superior time spend on biological motion in ESDM group versus control group after 2 years of treatment. the investigators also expect a significant superior orientation toward eyes in complex social scenes, an inferior shifting attention time and a superior preference for unpredictable stimuli in ESDM group versus ASD control group after 2 years. the investigators also expect that ESDM group would have time spend on biological motion, orientation toward eyes in complex scenes, shifting attention time and preference for unpredictable stimuli comparable to children without ASD after 2 years. This study would allow better understanding of ESDM active principles.

Registry
clinicaltrials.gov
Start Date
May 29, 2017
End Date
March 25, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hôpital le Vinatier
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Children 15 months to 36 months
  • Children with autism spectrum disorder (according to international criteria, ADI and ADOS)
  • DQ at 30 at least at the Early Learning Mullen Scale
  • Family domiciled within 40 minutes of an early intervention unit

Exclusion Criteria

  • Severe neurological or physical disorder identified in the child or family that would interfere with intervention
  • Unavailability of the family for regular monitoring of the child by the investigator center
  • Child with a Rett Sd or Childhood disintegrative disorders
  • Visual problems or with eyes in general

Outcomes

Primary Outcomes

The primary outcome will be the time spent on biological motion in the task of visual preference stimuli.

Time Frame: 2 years

2 different types of stimuli (dynamic biological or geometrical movements) are presented in parallel on each part of the screen alternatively (left and/ or right). Child sit at 60 cm from the screen of the Eye-tracker can look towards the one or the other one stimuli.

Secondary Outcomes

  • Average proximity from pattern eyes norm in complex social scene task(2 years)
  • Time spent on unpredictable stimuli(2 years)
  • Difference of saccadic latencies between overlap and gap condition(2 years)

Study Sites (1)

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