Efficiency of Early Intervention for Autism Spectrum Disorder

Autism Spectrum Disorder Clinical Trial

— IDEA  

Official title:

Impact of Early Intervention on the Global Development of Children With Autism Spectrum Disorder in a European French-speaking Population Dr Marie-Maude GEOFFRAY Le Vinatier Hospital

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02608333
• Other study ID #: 2015-A00124-45
• Status: Completed
• Phase: N/A
• Start date: September 9, 2015
• Est. completion date: June 30, 2021

Study information

• Verified date: February 2021
• Source: Hôpital le Vinatier
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Intervention for autism spectrum disorder (ASD) in European French-speaking countries is often heterogeneous and poorly evaluated. Six French-speaking early intervention units for children with ASD following the Early Start Denver Model (ESDM) have been created since 2011 with the common aim to evaluate effectiveness and cost-efficiency of the ESDM applied to the European French-speaking public health system. In those units, Children receive ESDM at minimum 12H per week by trained therapist. Therapist work in collaboration with parents (at home) and preschool or nursery. The first aim of the investigators study is to evaluate the effectiveness of ESDM intervention 12 hours per week during 2 years on the global development of children with ASD compared to the interventions commonly available in the community.

Description:

This is a multicenter (4 centers in France, 1 center in Switzerland and 1 center in Belgium), randomized, controlled, single blind trial using a modified Zelen design .It concerns children with ASD aged 18 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 a 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. Global developmental profiles of all the children will be measured at different time points over the two years through standardized tests such as the Mullen Scale of Early Learning (MSEL), the ADOS-2 and the Vineland Adaptive Behavior Scale. Cost of each intervention will be calculated. The primary outcome is global development of the child, measured by the developmental quotient with the Mullen after 24 months of intervention.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 180
• Est. completion date: June 30, 2021
• Est. primary completion date: June 30, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 15 Months to 36 Months

Eligibility

Inclusion Criteria:

• Children 15 months to 36 months
• Children with autism spectrum disorder (according to international criteria and standardized tests)
• Children at a DQ of 30 at least at the MSEL
• Family domiciled within 40 minutes of a early intervention unit (investigator center for the study)

Exclusion Criteria:

• Severe neurological or physical disorder identified not allowing intensive care
• Unavailability of the family for regular monitoring of the child by the investigator center
• Rett Syndrom

Related Conditions & MeSH terms

• Autism Spectrum Disorder
• Autistic Disorder
• Child Development Disorders, Pervasive

Intervention

Behavioral:
• ESDM-12
ESDM is a comprehensive relational, developmental and behavioral intervention. It's described in a manual for professional (Rogers et al, 2010). Children receive ESDM 12H per week by trained therapist. Therapist work in collaboration with parents (at home) and preschool or nursery.
• control group
heteregenous "as usual "community intervention

Locations

Country	Name	City	State
France	Hopital Vinatier	Bron	Aura

Sponsors (5)

Lead Sponsor	Collaborator
Hôpital le Vinatier	Centre hospitalier Saint Jean de Dieu - ARHM, Hospices Civils de Lyon, University Hospital, Strasbourg, France, Versailles Hospital

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Developmental quotient at the Mullen Scale of Early Learning	This criterion will be assessed with the Mullen scale of Early Learning (Mullen, 1995) by a psychologist blind of intervention group of the child:	Change from baseline in developmental quotient at 24 months follow-up
Secondary	Severity of autism symptoms is measured with ADOS 2	severity of autism symptoms is measured with ADOS 2 ( Autism Diagnostic observation Schedule 2)	Change from baseline in severity score of autism symptoms at 24 months follow-up
Secondary	Adaptive behavior score is measured by the composite score of Vineland adaptative behavior scale 2	Adaptative behavior score is measured by the composite score of Vineland adaptative behavior scale 2	Change from baseline in adaptative behavior at 24 months follow-up
Secondary	Productive language level assessed with a standardized French productive language developmental scale	This criterion will be assessed with a standardized French productive language developmental scale (DLPF "Development du language de production" in French language) filled by parents	change from baseline in number of words at 24 months follow-up (T2)
Secondary	Costs associated with interventions	Healthcare, social and personal resources devoted to child care throughout the study will be measured to evaluate the direct and indirect costs associated with intervention. Assessment will take place	at 24 months follow-up (T2)
Secondary	Developement of communication and symbolic behavior	Total score of Communication and Symbolic Behaviour Scale Developmental Profil CSBS-DP questionnaire for caregivers (Wetherby et al, 2002)	At baseline (inclusion ° T0), at 12 months follow-up (T1), and at 24 months follow-up
Secondary	Parent child naturalistic interaction during play	Dyadic Communication Measure for Autism (DCMA)(Green et al, 2010; Pickles, 2015) will be used and score of parent's communication synchrony, child initiation, and shared attention will be assessed	At baseline (inclusion ° T0), at 12 months follow-up (T1), and at 24 months follow-up (T2)
Secondary	Sensorial profil	Sensorial profil of Dunn	At baseline (inclusion ° T0), at 12 months follow-up (T1), and at 24 months follow-up (T2)
Secondary	Change at the Brief Observation of Social Communication Change (BOSCC)	The total score of Brief Observation of Social Communication Change	At baseline (inclusion ° T0), at 12 months follow-up (T1), and at 24 months follow-up