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Exploring an Evidence-Based, Culturally Adapted Family–Hospital Integrated Intervention Model for Autism Spectrum Disorder in China

Exploring an Evidence-Based, Culturally Adapted Family–Hospital Integrated Intervention Model for Autism Spectrum Disorder in China

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128424
Enrollment
Unknown
Registered
2026-07-20
Start date
2026-07-31
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autism spectrum disorder

Interventions

Control group:Intensive intervention based on applied behavior analysis (ABA), including basic parent education/training in ABA.
Experimental group:ABA combined with parent-implemented naturalistic developmental behavioral intervention (NDBI), primarily delivered through the Project ImPACT model.

Sponsors

Children's Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 8 Years

Inclusion criteria

Inclusion criteria: 1. Meeting the DSM-5 diagnostic criteria for Autism Spectrum Disorder, with an Autism Diagnostic Observation Schedule, Second Edition (ADOS-2) comparison score of >= 7, as confirmed by a multidisciplinary clinical team. 2. The primary caregiver (providing >= 20 hours of weekly companionship) is able to communicate in Mandarin, can understand the study content, provide written informed consent, and has no serious psychiatric or psychological disorders (e.g., major depressive disorder).

Exclusion criteria

Exclusion criteria: 1. Comorbid severe neurological disorders or unstable physical illnesses that would interfere with study participation. 2. Severe visual, auditory, or motor impairments that would affect the implementation of assessments/training. 3. Participation in other clinical trials or receipt of high-intensity, similarly structured programs within the past 6 months that could influence the outcomes of the present study. 4. Poor compliance as judged by the investigator, rendering the participant unable to complete the intervention according to the protocol.

Design outcomes

Primary

MeasureTime frame
Clinical Scale Assessments;

Secondary

MeasureTime frame
Brain Function Assessment;

Countries

China

Contacts

Public ContactChenxi Li

Children's Hospital, Zhejiang University School of Medicine

lichenxi@whu.edu.cn+86 571 88873321

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026