Parent-Mediated Social Cognition Intervention for Young Children With Autism Spectrum Disorder (PMSC-ASD)
Efficacy of a Parent-Mediated, Home-Based Structured Play Intervention on Social Cognitive Development in Young Children With Autism Spectrum Disorder: A Non-Randomized Controlled Study
This study evaluates the efficacy of the Companion Mind-Drawing Cooperative Game Program, a parent-mediated, home-based structured play intervention targeting social cognitive development in young children with autism spectrum disorder (ASD).
Children with ASD in the intervention group will receive a structured program in which parents attend an in-person training session (approximately 2.5 hours) at the hospital, where parents are taught to administer a series of researcher-designed cooperative game paradigms at home. Parents then deliver the intervention daily for at least 30 minutes per session over a period of six months. Monthly online video reviews by a clinician provide parents with individualized feedback and guidance to ensure program fidelity and quality.
Children with ASD in the comparison group will continue to receive usual care and will not receive the program during the study period.
Social cognitive outcomes - including emotion recognition, theory of mind, empathy, joint attention, self-perception, and social communication - will be assessed at baseline and at 12-month follow-up using behavioral experimental tasks and eye-tracking paradigms. This study aims to provide evidence for the efficacy of a scalable, family-implemented social cognition intervention for young children with ASD.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Background Social cognitive impairments - including difficulties in emotion recognition, theory of mind (ToM), empathy, joint attention, self-perception, and social communication - are hallmark features of ASD and significantly impact children's everyday social functioning. Despite the recognized importance of early social cognitive intervention, scalable and family-implemented programs that systematically target multiple social cognitive domains remain limited.
Intervention: "Companion Mind-Drawing Cooperative Game" Program
The "Companion Mind-Drawing Cooperative Game" program is a researcher-designed, parent-mediated intervention comprising a series of structured cooperative game paradigms, each targeting a specific social cognitive domain. The intervention is delivered in three phases:
- Parent Training (In-Person) Parents attend a structured training session of approximately 2.5 hours at the clinical site. During training, parents are taught the theoretical rationale for each game paradigm, the specific social cognitive skills targeted, and standardized procedures for home delivery.
- Home-Based Delivery Following training, parents deliver the intervention at home daily for a minimum of 30 minutes per session over a period of six months. The program targets six social cognitive domains: emotion recognition, theory of mind, empathy, joint attention, self-perception, and social communication.
- Monthly Clinician Supervision Once per month throughout the six-month intervention period, a clinician reviews video recordings submitted by parents and conducts an online video session to provide individualized feedback, address implementation challenges, and reinforce correct delivery techniques.
Comparison Group Participants in the comparison (treatment-as-usual) group continue to receive any existing therapies or educational support received prior to study enrollment. Participants in the comparison group do not receive the "Companion Mind-Drawing Cooperative Game" program during the study period.
Assessments All participants are assessed at two timepoints: baseline (prior to intervention commencement) and 12-month follow-up. Assessments include behavioral experimental tasks and eye-tracking paradigms targeting each of the six social cognitive domains addressed by the intervention.
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Chunchun Hu, Dr.
- Numéro de téléphone: +8615721445658
- E-mail: 14211240007@fudan.edu.cn
Lieux d'étude
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Chine, 201102
- Recrutement
- Children's Hospital of Fudan University
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Contact:
- Chunchun Hu
- Numéro de téléphone: 15721445658
- E-mail: 14211240007@fudan.edu.cn
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
Accepte les volontaires sains
La description
Inclusion Criteria:
Children：
- Aged 2.5 to 14 years at time of enrollment, with a primary recruitment focus on children aged 3 to 10 years.
- Meets diagnostic criteria for autism spectrum disorder (ASD) according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), confirmed by a specialist clinician.
- Full-scale intelligence quotient (FSIQ) ≥ 70 as assessed by an age-appropriate Wechsler intelligence scale administered.
- Possesses sufficient verbal ability to engage with structured play-based intervention activities, as judged by the recruiting clinician.
- Resides with and is cared for by a participating parent or legal guardian who meets the caregiver eligibility criteria below.
Caregiver：
- Is the primary caregiver (parent or legal guardian) of the enrolled child and resides in the same household.
- Is able and willing to attend an in-person parent training session (approximately 2.5 hours) at the study site prior to intervention commencement.
- Is able and willing to commit to administering the structured intervention program to the child for a minimum of 30 minutes per day throughout the 6-month intervention period.
- Is able and willing to participate in monthly online video supervision sessions with the study clinician.
- Has sufficient literacy and comprehension ability to understand program training materials and follow intervention procedures.
- Provides written informed consent on behalf of the child and for their own participation prior to any study procedures.
Exclusion Criteria:
Children：
- Known diagnosis of a genetic syndrome associated with ASD or intellectual disability, including but not limited to Fragile X syndrome, Down syndrome, tuberous sclerosis complex, or Rett syndrome.
- Presence of a neurological disorder, including epilepsy (unless fully controlled with stable medication for ≥ 12 months), acquired brain injury, cerebral palsy, or other significant neurological condition that may confound assessment of social cognition.
- Uncorrected vision or hearing impairment that would preclude participation in behavioral or eye-tracking assessments.
- Currently enrolled in another interventional clinical study targeting social cognition, communication, or behavioral outcomes.
- Any medical, psychiatric, or developmental condition that, in the opinion of the recruiting clinician, would interfere with the child's ability to participate in or benefit from the intervention.
Caregiver：
- Unable to attend the in-person parent training session at the study site due to geographic, occupational, or other constraints.
- Unable to commit to the daily home-based intervention schedule or monthly online supervision sessions for the full 6-month intervention period.
- Presence of significant mental health difficulties or other circumstances that, in the opinion of the recruiting clinician, would substantially impair the caregiver's ability to deliver the intervention with adequate fidelity.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Intervention Group
Parent-mediated structured play program; daily 30-min home sessions × 6 months; monthly clinician video supervision
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Parent-mediated structured play program; daily 30-min home sessions × 6 months; monthly clinician video supervision
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Aucune intervention: Treatment-as-Usual Control Group
Continues existing therapies/educational support; no additional intervention provided
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in Social Attention (Eye-Tracking)
Délai: Baseline →6-month →12-month（11-13mo） follow-up
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The mean fixation proportion (percentage of total trial time) allocated to socially relevant regions of interest (ROIs) - including faces, eyes, and mouth regions - during standardized eye-tracking paradigms, measured via a remote eye-tracker.
A higher fixation proportion indicates greater social attention.
Change scores are calculated as the difference between follow-up and baseline fixation proportions.
|
Baseline →6-month →12-month（11-13mo） follow-up
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Change in Theory of Mind Task Accuracy Score
Délai: Baseline →6-month →12-month（11-13mo） follow-up
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The mean accuracy score (percentage of correct responses) on a battery of researcher-designed Theory of Mind (ToM) behavioral experimental tasks
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Baseline →6-month →12-month（11-13mo） follow-up
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Parent intervention fidelity
Délai: Months 1-6 (intervention group only)
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The total score on a video-coded fidelity checklist completed by trained assessors reviewing monthly parent-submitted video recordings.
The checklist evaluates adherence to standardized delivery procedures across domains including correct game administration, appropriate prompting strategies, session duration, and responsiveness to the child.
Scores range from 0-100, with higher scores indicating greater fidelity.
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Months 1-6 (intervention group only)
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Change in Scores of Emotion recognition accuracy
Délai: Baseline →6-month →12-month（11-13mo） follow-up
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The mean proportion of correct responses (accuracy rate) on standardized emotion recognition paradigms, in which children are asked to identify or match basic and complex emotional expressions (e.g., happy, sad, angry, fearful, surprised) presented via images or short video clips.
Change scores are calculated as the difference in accuracy rate between follow-up and baseline assessments.
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Baseline →6-month →12-month（11-13mo） follow-up
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Parent program satisfaction
Délai: Post-intervention (6 months)
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The total score on a structured parent feedback questionnaire assessing satisfaction with the program content, delivery format, training quality, clinician supervision, and perceived benefit for the child.
The questionnaire uses a Likert-scale format (e.g., 1-5), with higher scores indicating greater satisfaction.
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Post-intervention (6 months)
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Empathy, Self-perception, Social communication
Délai: Baseline →6-month→ 12-month(11-13mo) follow-up
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The mean proportion of correct responses (accuracy rate) on researcher-designed behavioral experimental tasks targeting three social cognitive domains: (a) Empathy - tasks requiring recognition and attribution of others' emotional states in social scenarios; (b) Self-perception - tasks assessing self-recognition and self-referential processing; (c) Social Communication - tasks evaluating pragmatic language use, referential communication, and conversational turn-taking.
Each domain is scored separately, and a composite score is also calculated.
Change scores are calculated as the difference between follow-up and baseline accuracy rates for each domain.
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Baseline →6-month→ 12-month(11-13mo) follow-up
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Xiu Xu, Prof., Children's Hospital of Fudan University
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- TBXHP-ASD
Plan pour les données individuelles des participants (IPD)
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Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
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