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Recruiting NCT05726708

Impact of an E-Learning Coaching for Parents of Young Children With Autism

No phase Interventional Autism Spectrum Disorder

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: E-Learning.
Who it may be relevant to
Registry conditions: Autism Spectrum Disorder. Basic parameters: 24 months — 48 months · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Switzerland
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Impact of an E-Learning Parental Coaching for Parents of Young Children With Autism Spectrum Disorder

Overview

The goal of this study is to evaluate the impact of a parental coaching based on E-Learning (EL), intended for parents of children with autism spectrum disorder (ASD). Population: parents of young children (2 to 4 years old) with an ASD diagnosis. The main questions that our study will answer are: * Has parental coaching via E-Learning a significant impact compared to no coaching? * If so, is that impact comparable to standard parental coaching such as PACT? The impact will be evaluated in three domains: * Child development: behavior, sleep, eating behavior * Parental competences: stress, coping, feeling of parental competencies * Parent-child interaction: communication, visual attention The investigators will compare 3 groups: 1. ASD children whose parents will follow a parental coaching via E-learning, 2. ASD children whose parents will follow a standard parental coaching (PACT) 3. ASD children whose parents will not follow any specific coaching program

Interventions

  • Behavioral E-Learning
    On line modules of coaching for parents

Primary outcome measures

  • Dyadic Communication Measure for Autism (DCMA) before parental coaching [Time frame: Month 0]
  • Dyadic Communication Measure for Autism (DCMA) immediately after the end of parental coaching [Time frame: Month 6]
  • Dyadic Communication Measure for Autism (DCMA) 6 months after the end of parental coaching [Time frame: Month 12]
  • Brief Observation of Social Communication Change (BOSCC) before parental coaching [Time frame: Month 0]
  • Brief Observation of Social Communication Change (BOSCC) immediately after the end of parental coaching [Time frame: Month 6]
  • Brief Observation of Social Communication Change (BOSCC) 6 months after the end of parental coaching [Time frame: Month 12]
  • Percentage of synchronized communication acts with the parents and professionals before parental coaching [Time frame: Month 0]
  • Percentage of synchronized communication acts with the parents and professionals immediately after the end of parental coaching [Time frame: Month 6]
  • Percentage of synchronized communication acts with the parents and professionals 6 months after the end of parental coaching [Time frame: Month 12]
  • Mullen Scales of Early Learning (MSEL) before parental coaching [Time frame: Month 0]

Eligibility criteria

Inclusion criteria

  • Children with ASD
  • Age 2 years to 4 years and 6 months
  • Family speaking french
  • Parent who signed the consent form

Exclusion criteria

  • children with known genetic syndrome
  • children with visual or auditive deficit
  • children with epilepsy
  • no internet access
  • no french speaking

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Switzerland · 1 center
  • Service des troubles du spectre de l'autisme et apparentés — Lausanne

Identifiers

NCT: NCT05726708 · 552

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗