Parent-implemented Social Communication Treatment in Preschool Children With Autism Spectrum Disorder

Sponsor
Chinese University of Hong Kong (Other)
Overall Status
Recruiting
CT.gov ID
NCT05635760
Collaborator
(none)
112
2
2
44.9
56
1.2

Study Details

Study Description

Brief Summary

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 a Group format (up to 8 families learning together) is more effective than treatment learnt by the parents themselves in a Passive Control format (learning the same materials without the guidance of a therapist) at the study level. The investigators will then evaluate what combinations of parent and child behavioral 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 Group 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Group-based Parent-implemented Social Communication Training
  • Behavioral: Self-learning-based Parent-implemented Social Communication Training
N/A

Detailed Description

For parents of children with Autism Spectrum Disorder (ASD), the primary concern is to minimize the impact of the disorder, likely through evidence-based intervention. The secondary concern is whether any intervention prescribed is affordable and the logistics of completion feasible. This project will obtain evidence for ASD intervention options that have different costs and intervention delivery formats (group vs. passive control) to evaluate whether a more costly option is more effective at the study level. The investigators will then develop a predict to-prescribe approach that informs parents which intervention option would likely be most cost-effective in light of each family's unique characteristics (i.e., effectiveness at the individual-child level). [We use the term "parents" to mean caregivers throughout this protocol.]

ASD affects 14 per 10,000 (0.14%) children in Hong Kong and 39.23 per 10,000 in Mainland China. Social communication is a deficit domain of ASD, and about 29% of preschoolers with ASD have severe verbal deficits. Intervention through pharmaceutical means remains elusive, leaving behavioral interventions the most realistic and immediate avenue of treatment. This project will focus on enhancing the cost-effectiveness of behavioral intervention that targets language and communication. The investigators will do so in the context of precision medicine, in which the investigators aim to identify the most cost effective intervention for the individual child with ASD.

AIM OF STUDY:

Objective 1: The investigators will first ascertain whether parent-implemented communication treatment taught by a speech therapist in a Group format (up to 8 families learning together) is more effective than treatment learnt by the parents themselves in a Passive Control format (learning the same materials without the guidance of a therapist) at the study level.

Objective 2: The investigators will examine pre-treatment child and parent variables simultaneously and construct predictive models of response to the two treatment options (group, more costly vs. passive control, less costly) at the individual-child level.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
112 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Predict-to-Prescribe Approach to Social Communication Treatment in Chinese Preschool Children With Autism Spectrum Disorder
Actual Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Jun 30, 2025
Anticipated Study Completion Date :
Jun 30, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group-based Parent-implemented Social Communication Training

Behavioral: Group-based Parent-implemented Social Communication Training
The intervention will be taught by a speech therapist online (approximately 25 hours distributed over 6 months), with up to 8 parents in a group.

Active Comparator: Self-learning-based Parent-implemented Social Communication Training

Behavioral: Self-learning-based Parent-implemented Social Communication Training
Self-learning families will learn the same materials without the guidance of a therapist.

Outcome Measures

Primary Outcome Measures

  1. Change from Baseline Social Affect at 12 months [Baseline and at 12 months after the beginning of treatment]

    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 outcomesubscore of Autism Diagnostic Observation Scheduleā„¢, Second Edition (ADOS-2) between groups

Secondary Outcome Measures

  1. Change from Baseline Number of Parent-child Turn-taking at 6 months and 12 months [Baseline, at 6 months and at 12 months after the beginning of treatment]

    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.

  2. Change from Baseline Mean Length of Utterance at 6 months and 12 months [Baseline, at 6 months and at 12 months after the beginning of treatment]

    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.

  3. Change from Baseline Number of Nouns and Verbs at 6 months and 12 months [Baseline, at 6 months and at 12 months after the beginning of treatment]

    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

  4. Change from Baseline Prosody in terms of loudness variation at 6 months and 12 months [Baseline, at 6 months and at 12 months after the beginning of treatment]

    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.

  5. Change from Baseline Prosody in terms of fundamental frequency at 6 months and 12 months [Baseline, at 6 months and at 12 months after the beginning of treatment]]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
24 Months to 60 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

  • Social Communication Questionnaire (SCQ) score greater than or equal to 15.

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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Shenzhen Research Institute, The Chinese University of Hong Kong Shenzhen Guangdong China 518057
2 The Chinese University of Hong Kong Hong Kong Shatin Hong Kong

Sponsors and Collaborators

  • Chinese University of Hong Kong

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Patrick C. M. Wong, Stanley Ho Professor of Cognitive Neuroscience; Director of Brain and Mind Institute, Chinese University of Hong Kong
ClinicalTrials.gov Identifier:
NCT05635760
Other Study ID Numbers:
  • CRFASD-SZ-22
First Posted:
Dec 2, 2022
Last Update Posted:
Dec 2, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Patrick C. M. Wong, Stanley Ho Professor of Cognitive Neuroscience; Director of Brain and Mind Institute, Chinese University of Hong Kong
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 2, 2022