Autism Spectrum Disorder Clinical Trial
Official title:
A Predict-to-Prescribe Approach to Social Communication Treatment in Chinese Preschool Children With Autism Spectrum Disorder
NCT number | NCT05455411 |
Other study ID # | CRFASD-22 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | July 1, 2022 |
Est. completion date | June 30, 2026 |
An accumulation of research evidence has pointed to parent-implemented communication treatment as effective in reducing the severity of social communication deficits in preschool children with ASD. Despite even high-quality evidence, real-world translation to clinical practice remains challenging, especially for children from lower-income families, for two reasons. First, the treatment outcome is highly variable despite study-level efficacy data, most likely due to unique child and parent factors that make treatment response uneven across individual children. Second, the cost of intervention with the largest effect sizes remains high due to its one-on-one format. With the overarching goal to reduce cost and to increase treatment effectiveness at the individual-child level, this project will conduct a randomized controlled trial (RCT) to compare the effectiveness of two options for intervention to address two specific objectives. The investigators will first ascertain whether parent-implemented communication treatment taught by a speech therapist in an Individual (one-on-one) format is more effective than treatment taught in a Group format (up to 8 families learning together) at the study level. The Individual format is at least 4 times more expensive than the Group format; its relative treatment effect must be empirically ascertained to justify its cost. The investigators will then evaluate what combinations of parent and child behavioral and neural factors determine which format of intervention is likely to be more effective at the individual-child level. It is likely that not all families require the more costly Individual format of intervention. Machine-learning analytics with cross-validation will be used in constructing predictive models of treatment response, which will increase the likelihood of these models being generalizable to new patients. This study will be among the first examples of fulfilling the promise of Precision Medicine in providing guidance to patients and families with developmental disorders not about whether to receive intervention but which option for intervention to receive in the context of multiple options. This predict-to-prescribe approach of ASD intervention will likely lead to a paradigm shift in clinical practice and ultimately result in lowering the overall cost and increasing the effectiveness of intervention for children with ASD as individuals.
Status | Recruiting |
Enrollment | 112 |
Est. completion date | June 30, 2026 |
Est. primary completion date | June 30, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Months to 60 Months |
Eligibility | Inclusion Criteria: - Have a confirmed diagnosis of autism spectrum disorder or was evaluated to have elevated likelihood ("at-risk" or "suspected") by a Clinical Psychologist, Psychiatrist or Pediatrician who recommended continuous surveillance. - ADOS-2 score in the spectrum range (for Modules 1 & 2) or mild-to-moderate concern range (for Toddler Module) Exclusion Criteria: - Mullen Scale of Early Learning non-verbal age at or less than 12 months - Parent who has severe psychological or neurological conditions prohibiting them from conducting the treatment program at home (restricted to only the parent in the program) - Children with any other severe developmental problems beyond autism spectrum disorder |
Country | Name | City | State |
---|---|---|---|
Hong Kong | The Chinese University of Hong Kong | Shatin | |
Hong Kong | Castle Peak Hospital | Tuen Mun |
Lead Sponsor | Collaborator |
---|---|
Chinese University of Hong Kong |
Hong Kong,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from Baseline Social Affect at 12 months | Comparing the pre- and post-treatment social affect measured by the Social Affect subscore of Autism Diagnostic Observation Scheduleā¢, Second Edition (ADOS-2) between groups.
The Social Affect subscore of ADOS-2 ranges from 0 to 20; the higher ADOS-2 scores mean a worse outcome. |
Baseline and at 12 months after the beginning of treatment | |
Secondary | Change from Baseline Number of Parent-child Turn-taking at 6 months and 12 months | Comparing the pre- and post-treatment number of parent-child turn-taking between groups.
A parent-child interaction video will be taken; the number of turn-taking will be counted. The greater number of the mentioned language and communication features mean a better outcome. |
Baseline, at 6 months and at 12 months after the beginning of treatment | |
Secondary | Change from Baseline Mean Length of Utterance at 6 months and 12 months | Comparing the pre- and post-treatment mean length of utterance between groups.
A parent-child interaction video will be taken; speech of children will be transcribed. The length of utterance will be assessed and the mean length of utterance will be calculated. The longer mean length of utterance mean a better outcome. |
Baseline, at 6 months and at 12 months after the beginning of treatment | |
Secondary | Change from Baseline Number of Nouns and Verbs at 6 months and 12 months | Comparing the pre- and post-treatment number of nouns and verbs between groups.
A parent-child interaction video will be taken; speech of children will be transcribed. The number of nouns and verbs will be counted. The greater number of nouns and verbs means a better outcome. |
Baseline, at 6 months and at 12 months after the beginning of treatment | |
Secondary | Change from Baseline Prosody in terms of loudness variation at 6 months and 12 months | Comparing the pre- and post-treatment loudness variation between groups.
A parent-child interaction video will be taken. Audio with the speech of children will be extracted. Loudness of the audio will be assessed with Praat, an acoustic analysis software. The reduction of the loudness variation means a better outcome. |
Baseline, at 6 months and at 12 months after the beginning of treatment | |
Secondary | Change from Baseline Prosody in terms of fundamental frequency at 6 months and 12 months | Comparing the pre- and post-treatment fundamental frequency between groups.
A parent-child interaction video will be taken. Audio with the speech of children will be extracted. The fundamental frequency of the audio will be assessed with Praat, an acoustic analysis software. The reduction of fundamental frequency means a better outcome. |
Baseline, at 6 months and at 12 months after the beginning of treatment |
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