Autism Spectrum DisorderImPACTNCT07393893
The Effects and Mechanism of Parent Intervention for Autism Sprectrum Disorder
A study testing Parents conducted interventions based on project ImPACT. and General behavioral interventions in people with Autism Spectrum Disorder, run by University of Electronic Science and Technology of China at 1 site in China.
Trial summary
Purpose of the Research: The goal of this clinical study is to investigate if a parent training program called "Project IMPACT" (Improving Parents as Communication Teachers) can help improve the core challenges in social interaction and communication for children with Autism Spectrum Disorder (ASD). Read more about this study
- Who is it for?
- Ages 18 to 78 months
- Conditions the study is for
- Autism Spectrum Disorder
- What is being tested?
- Parents conducted interventions based on project ImPACT. and General behavioral interventions
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- 1 siteChina
- Study dates
- 8 Oct 2024to 1 Dec 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 78 months
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Participants must be between the ages of 18 months and 78 months (6.5 years) at the time of enrollment.
- Participants must have received a formal diagnosis of autism spectrum disorder (or meet criteria for conditions within the autism spectrum) from qualified clinicians, such as psychiatrists or pediatricians, in accordance with the diagnostic criteria specified in either the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) or the International Classification of Diseases, 11th Revision (ICD-11).
- Participants must have a score meeting the autism spectrum cutoff on the Autism Diagnostic Observation Schedule, Second Edition (ADOS-2).
- At least one parent is able to participate in the entire assessment and intervention procedure.
Who cannot join
- Presence of a comorbid major neurological disorder (e.g., epilepsy, cerebral palsy) or a severe psychiatric condition.
- A history of significant brain injury or trauma.
- Current use of psychotropic medication or a within 3 months history of receiving transcranial electrical/magnetic stimulation therapy.
- Significant uncorrected impairment in visual or auditory acuity.
- Motor function disorders.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
China1 site
Chengdu women's and children's central hospital
Chengdu, Sichuan, 610000
About this study
Official title: The Effects of Parent-based IMPACT Intervention for Autism Sprectrum Disorder and Its Related Neural Mechanism
Purpose of the Research:
The goal of this clinical study is to investigate if a parent training program called "Project IMPACT" (Improving Parents as Communication Teachers) can help improve the core challenges in social interaction and communication for children with Autism Spectrum Disorder (ASD). And to explore whether and how this intervention affects children's brain activity.
Read more
Key Questions This Study Aims to Answer:
Does participation in the IMPACT parent training program significantly improve ASD symptoms, social communication abilities, and adaptive functioning in daily life for children with ASD compared to general intervention?
Study Design:
This is a assessor blinding randomized controlled trial. Participating children will be randomly assigned to one of two groups: IMPACT Intervention Group with primary caregiver conducting intervention and Control Group with current routine interventions provided by behavioral trainers.
The research team will evaluate all children at three time points: before the intervention starts, immediately after the 10 - week intervention period, and 6 months after the intervention ends. The measurements include social - related questionnaires, ADOS - 2, Griffiths Scales, eye - tracking, task - based fNIRS, and fMRI without sedation.
Read the detailed description
Purpose of the Research:
The goal of this clinical study is to investigate if a parent training program called "Project IMPACT" (Improving Parents as Communication Teachers) can help improve the core challenges in social interaction and communication for children with Autism Spectrum Disorder (ASD). And to explore whether and how this intervention affects children's brain activity. We will use safe brain imaging techniques (such as MRI and functional Near-Infrared Spectroscopy, fNIRS) to compare changes in the brain before and after the intervention, aiming to understand the potential brain mechanisms behind behavioral progress. Ultimately, we hope to identify which types of children might benefit most from this intervention, providing insights for more personalized treatment recommendations in the future.
Key Questions This Study Aims to Answer:
Does participation in the IMPACT parent training program significantly improve ASD symptoms, social communication abilities, and adaptive functioning in daily life for children with ASD compared to general intervention?
Study Design:
This is a assessor blinding randomized controlled trial. Participating children will be randomly assigned to one of two groups:
IMPACT Intervention Group (approximately 40 children): The primary caregivers of these children will receive a systematic IMPACT training course over about 10 weeks (including group sessions and individual coaching), learning how to apply these techniques during interactions at home. All caregiver will be encouraged to conduct intervention at least 10 hours per week.
Control Group (approximately 40 children): The caregivers of these children will not receive IMPACT training during the initial 10-week period. They are encouraged to continue any current routine interventions their child is receiving. After 10 weeks, they will be offered the opportunity to receive the IMPACT training online for free as compensation.
Intervention Component (Exclusively for families randomly assigned to the ImPACT group):
Primary caregivers of participants will partake in the approximately 10 - week IMPACT parent training program. In weeks with odd numbers, caregivers will attend a group theory session lasting 3 - 4 hours. In weeks with even numbers, caregivers will receive a one - on - one coaching session (1 - 1.5 hours) with a trainer to enhance their intervention skills based on ImPACT. Caregivers are obligated to implement the learned strategies during daily home interactions with participants for a minimum of 10 hours per week and maintain a simple record of these activities. Trainers will monitor adherence via weekly reviews of activity logs and coaching sessions. Adherence will be further bolstered by real - time feedback during coaching sessions, where trainers prompt caregivers to engage their child in task - oriented activities while demonstrating and suggesting effective strategies, ensuring skill generalization in naturalistic settings.
The research team will evaluate all children at three time points: before the intervention starts, immediately after the 10-week intervention period, and 6 months after the intervention ends. The assessors will not know which group each child belongs to (they will be "blinded") to ensure objective results.
What the Involvement of Participation Entails:
If your child (aged 1.5 to 6.5 years) has a diagnosis of ASD and you agree to participate, the following may be involved:
Assessment Sessions (Three times: Pre-intervention, Post-intervention at 10 weeks, only SRS-2 measured after 6 months):
Questionnaires: You will be asked to fill out questionnaires about your child's behavior, social skills, and your own experiences and stress levels.
Child Assessments: A trained clinician, independent of the research team, will conduct standardized assessments of your child's development and social communication skills (e.g., ADOS-2, Griffiths Scales).
Eye-Tracking Test: Your child will watch short videos while a specialized, non-invasive device records where and for how long your child looks. This helps us understand their visual attention preferences towards social information.
Functional Near-Infrared Spectroscopy (fNIRS): During a play session, your child will wear a soft cap with sensors. It uses harmless near-infrared light to measure changes in brain activity in the outer layer of the brain. This procedure is safe, non-invasive, and radiation-free.
Magnetic Resonance Imaging (MRI) Scan (voluntary): We plan to conduct one brain MRI scan before and after the intervention for all willing participants to study brain structure and function. To ensure the child remains still during the scan, we plan to perform it during natural, deep sleep.
Voluntary Participation:
Participation in this study is completely voluntary. You may decide to withdraw yourself and your child from the study at any time, for any reason, without any penalty or effect on the future medical care you receive at this hospital or elsewhere.This study will be submitted for ethical review to ensure it meets scientific and ethical standards, protecting the rights, safety, and well-being of every participant.
- Conditions
- Autism Spectrum Disorder
- Being tested
- Parents conducted interventions based on project ImPACT., General behavioral interventions
- Keywords
- AUTISM, PARENT INTERVENTION, MECHANISM
- Medical subject headings
- Autism Spectrum Disorder, Autistic Disorder
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Parents conducted interventions based on project ImPACT.Behavioural
Also called ImPACT
Parents conduct behavioral interventions under the supervision of professional trainers who have obtained the certificate of Project IMPACT training. They are encouraged to conduct the interventions at least 10 hours per week without receiving other interventions from institutions or hospitals. Parents are asked to record the activities and duration of intervention they conducted daily in a logbook, which is reviewed weekly by certified trainers to ensure fidelity and provide feedback. Adherence is monitored through every other week one-one session to review progress, address challenges, and refine strategies. Trainers emphasize consistent implementation of evidence-based techniques, ensuring parents maintain high fidelity to the ImPACT model.
General behavioral interventionsBehavioural
Children were subjected to interventions administered by behavioral trainers from hospitals or institutions. We advocated for them to persist with the existing interventions of any type (such as Applied Behavior Analysis, Discrete Trial Training, sensory integration, and language therapy) and augment the sessions to achieve a total of 10 hours per week, either in group or individual settings. Parents are asked to document the duration and type of sessions their children participated in each week in a notebook.
| Study group | Role | What they receive |
|---|---|---|
| ImPACT-based Interventions | Experimental | Parent-based behavioral interventions for children. Receives: Behavioral: Parents conducted interventions based on project ImPACT. |
| General interventions | Active comparator | Current routine interventions provided by behavioral trainers. Receives: Behavioral: General behavioral interventions |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Autism Symptom Severity as measured by ADOS-2 Comparison Score and Subscales
The ADOS-2 (Autism Diagnostic Observation Schedule, Second Edition) is a semi-structured, standardized assessment of communication, social interaction, play, and restricted and repetitive behaviors. The Comparison Score is a standardized metric used to compare autism severity across different modules and ages. The Comparison Score ranges from 1 to 10, with higher scores indicating greater severity of autism spectrum-related symptoms (worse outcome).
Measured: From enrollment to the end of treatment at 10 weeks.
Change in Social Impairment as measured by the Social Responsiveness Scale, Second Edition (SRS-2) Total Score
The SRS-2 is a 65-item caregiver-completed rating scale that measures the severity of autism spectrum symptoms as they occur in natural social settings. Each item is scored on a 4-point Likert scale ranging from 0 (Never True) to 3 (Almost Always True). The Total Raw Score is calculated by summing the scores of all 65 items. The total raw score ranges from 0 to 195, with higher scores indicating greater severity of social impairment (worse outcome).
Measured: From enrollment to the end of treatment at 10 weeks, 3months after treatment.
Change in Child PFC Activation (Oxy-Hb) during Parent-Child Interaction
Mean Oxygenated Hemoglobin (Oxy-Hb) concentration in the Prefrontal Cortex (PFC) collected while the child engages in a standardized play task with their parent. Higher concentration indicates greater activation.
Measured: From enrollment to the end of treatment at 10 weeks.
Change in Social Visual Preference Index (Percentage of Fixation Duration)
Participants view a battery of 3 paired paradigms presenting simultaneous social and non-social stimuli. The index is calculated as the percentage of total fixation duration spent on Social Areas of Interest (AOIs) divided by the total fixation duration on both Social and Non-social AOIs. Formula: (Duration on Social / (Duration on Social + Duration on Non-social)) * 100. The score is averaged across the 3 paradigms. Values range from 0 to 100%. Higher scores indicate a stronger preference for social stimuli.
Measured: From enrollment to the end of treatment at 10 weeks.
Secondary outcomes (13)
Change in Adaptive Functioning as measured by the ABAS-II General Adaptive Composite (GAC) and Domain Scores
The ABAS-II (Adaptive Behavior Assessment System, Second Edition) measures adaptive skills across the lifespan. It provides a General Adaptive Composite (GAC) score and three composite domain scores: Conceptual, Social, and Practical. These are reported as age-adjusted Standard Scores. The standard score range is 40 to 160 (Mean = 100, SD = 15). Unlike symptom scales, higher scores indicate better adaptive functioning (better outcome).
Measured: From enrollment to the end of treatment at 10 weeks.
Change in Structural Brain Volume (Gray Matter Volume) in Regions of Interest (e.g., Prefrontal Cortex, Amygdala
Structural MRI data (T1-weighted) is collected during natural sleep. The metric reported is the Gray Matter Volume in specific Regions of Interest (ROIs) related to social processing.
Data is preprocessed using standard pipelines (e.g., FreeSurfer). Values are reported in cubic millimeters ($mm^3$).
Measured: From enrollment to the end of treatment at 10 weeks.
Change in Caregiver Burden as measured by the Caregiver Strain Questionnaire (CSQ) Total Score
The CSQ is a 21-item self-report measure used to assess the impact of caring for a child with emotional or behavioral disorders. It evaluates three domains: Objective Strain, Subjective Internalized Strain, and Subjective Externalized Strain. Items are rated on a 5-point scale ranging from 1 (Not at all a problem) to 5 (Very much a problem). The Total Score is calculated by summing the scores of all 21 items. The total score ranges from 21 to 105, with higher scores indicating higher levels of caregiver strain (worse outcome).
Measured: From enrollment to the end of treatment at 10 weeks.
Change in Parenting Sense of Competence (PSOC): Total Score and Subscales
he PSOC is a 17-item self-report scale assessed on a 6-point Likert scale. It comprises two subscales: Satisfaction (9 items, reflecting the parent's motivation and frustration) and Efficacy (8 items, reflecting the parent's perceived competence and problem-solving ability). Items in the Satisfaction dimension are reverse-coded so that higher scores reflect greater satisfaction. The Total Score is the sum of all 17 items, ranging from 17 to 102. Subscale scores range from 9-54 (Satisfaction) and 8-48 (Efficacy). Higher scores indicate higher parenting self-esteem and better coping capability (better outcome).
Measured: From enrollment to the end of treatment at 10 weeks.
Change in Repetitive Behaviors as measured by the Repetitive Behavior Scale-Revised (RBS-R) Total Score
The RBS-R is a caregiver-rated questionnaire designed to measure the breadth and severity of repetitive behaviors in individuals with autism. It typically consists of 43 items grouped into six subscales (Stereotyped, Self-injurious, Compulsive, Ritualistic, Sameness, and Restricted Behavior). Each item is rated on a 4-point Likert scale ranging from 0 (Behavior does not occur) to 3 (Behavior occurs and is a severe problem). The Total Raw Score is the sum of all 43 items, ranging from 0 to 129. Higher scores indicate greater severity of repetitive behaviors (worse outcome).
Measured: From enrollment to the end of treatment at 10 weeks
Change in Social Communication Skills as measured by the Project ImPACT Social Communication Checklist (Parent-Reported)
he Social Communication Checklist is a psychometrically validated measure designed for the Project ImPACT intervention (Wainer, Berger, \& Ingersoll, 2017). It assesses child progress across four domains: Social Engagement, Expressive Communication, Receptive Communication, and Imitation/Play. Items are scored on a frequency scale: 1 (Rarely/Not yet), 2 (Sometimes), and 3 (Frequently). (Note: Specific items 32-36 have weighted scoring for verbal/non-verbal strategies). The Total Score is the sum of all item scores, ranging from 70 to 215. Higher scores indicate better social communication skills (better outcome).
Measured: From enrollment to the end of treatment at 10 weeks.
ADOS-2 Raw Scores (Module 1 and Module 2)
Raw scores for the Social Affect (SA) and Restricted and Repetitive Behavior (RRB) domains, as well as the Overall Total Score. The specific algorithm (Module 1 "Few to No Words", Module 1 "Some Words", Module 2 "Younger than 5", or Module 2 "Older than 5") is determined by the participant's age and language level. Scores are summed, with higher scores indicating greater severity of autism spectrum-related symptoms (worse outcome). Scale Ranges: Social Affect (SA): 0 to 21, Restricted and Repetitive Behavior (RRB): 0 to 8, Total Score: 0 to 29 (Note: Maximum possible scores vary slightly by the specific algorithm used, but fall within these ranges.)
Measured: Baseline and Week 10
Change in Child PFC Activation (Oxy-Hb) during Interaction with Therapist
Mean Oxy-Hb concentration in the PFC collected while the child plays with a therapist (unfamiliar adult). Used to assess generalization of social brain response.
Measured: Baseline and Week 10
Change in Child PFC Activation (Oxy-Hb) during Solitary Play
Mean Oxy-Hb concentration in the PFC collected while the child plays alone (non-social condition). Serves as a control condition for social tasks.
Measured: Baseline and Week 10
Change in Social Orienting Index (Percentage of Fixation Counts)
Calculated as the percentage of discrete fixation counts directed towards Social AOIs relative to the total number of fixations on both stimuli types. Formula: (Count on Social / Total Count) * 100. Averaged across the 3 paradigms. Values range from 0 to 100%.
Measured: Baseline and Week 10.
Change in Intrinsic Functional Connectivity (Resting State fMRI)
Resting-state functional MRI is collected during natural sleep to assess intrinsic brain organization. The metric is the Functional Connectivity strength (Fisher's z-transformed correlation coefficient) within the Default Mode Network (DMN) or between social brain regions. Values range from -1 to 1 (approximate, after transformation). Higher values indicate stronger functional synchronization between regions.
Measured: Baseline and Week 10
Change in Parent Intervention Fidelity as measured by the Project ImPACT Fidelity of Implementation Rating Scale
Assessed in the intervention group only.Parent fidelity is assessed by trained independent observers using the Project ImPACT Fidelity Checklist. The scale evaluates the parent's competence in five intervention domains: 1) Focus on the Child, 2) Adjust Communication, 3) Create Opportunities, 4) Teach New Skills, and 5) Shape the Interaction. Each domain is rated on a 5-point Likert scale ranging from 1 (Low Fidelity/Ineffective) to 5 (High Fidelity/Effective). The Total Score is reported as the Mean Score across all applicable items/domains. The range is 1 to 5. Higher scores indicate higher fidelity and competence in delivering the intervention (better outcome).
Measured: Baseline and Week 10
Change in Social Communication Skills as measured by the Project ImPACT Social Communication Checklist (Teacher/Coach-Reported)
Assessed for the intervention group only. Completed by the teacher/interventionist to validate skill acquisition for the Project ImPACT intervention.It assesses child progress across four domains: Social Engagement, Expressive Communication, Receptive Communication, and Imitation/Play. Items are scored on a frequency scale: 1 (Rarely/Not yet), 2 (Sometimes), and 3 (Frequently). (Note: Specific items 32-36 have weighted scoring for verbal/non-verbal strategies). The Total Score is the sum of all item scores, ranging from 70 to 215. Higher scores indicate better social communication skills (better outcome).
Measured: Baseline and Week 10
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Feb 2026
- Study start8 Oct 2024
- Primary completion1 Jul 2026 (estimated)
- Study completion1 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Autism Spectrum DisorderStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 80 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Electronic Science and Technology of China
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Weihua Zhao, University of Electronic Science and Technology of China
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07393893
- Sponsor's protocol ID
- UESTC-neuSCAN-101
- Acronym
- ImPACT
- Status last verified
- Jan 2026
- First submitted
- 10 Dec 2025
- Last updated
- 6 Feb 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effects of Parent-based IMPACT Intervention for Autism Sprectrum Disorder and Its Related Neural Mechanism
- ClinicalTrials.gov ID
- NCT07393893
- Acronym / sponsor ID
- ImPACT / UESTC-neuSCAN-101
- Conditions
- Autism Spectrum Disorder
- Keywords
- AUTISM, PARENT INTERVENTION, MECHANISM
- Study type
- Interventional
- Recruitment status
- Enrolling by invitation
- Enrolment
- 80 participants (estimated)
- Lead sponsor
- University of Electronic Science and Technology of ChinaUniversity, hospital or other
- Study start
- 8 Oct 2024 (actual)
- Primary completion
- 1 Jul 2026 (estimated)
- Study completion
- 1 Dec 2026 (estimated)
- First posted
- 6 Feb 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Purpose of the Research:
The goal of this clinical study is to investigate if a parent training program called "Project IMPACT" (Improving Parents as Communication Teachers) can help improve the core challenges in social interaction and communication for children with Autism Spectrum Disorder (ASD). And to explore whether and how this intervention affects children's brain activity.
Key Questions This Study Aims to Answer:
Does participation in the IMPACT parent training program significantly improve ASD symptoms, social communication abilities, and adaptive functioning in daily life for children with ASD compared to general intervention?
Study Design:
This is a assessor blinding randomized controlled trial. Participating children will be randomly assigned to one of two groups: IMPACT Intervention Group with primary caregiver conducting intervention and Control Group with current routine interventions provided by behavioral trainers.
The research team will evaluate all children at three time points: before the intervention starts, immediately after the 10 - week intervention period, and 6 months after the intervention ends. The measurements include social - related questionnaires, ADOS - 2, Griffiths Scales, eye - tracking, task - based fNIRS, and fMRI without sedation.
Detailed description
Purpose of the Research:
The goal of this clinical study is to investigate if a parent training program called "Project IMPACT" (Improving Parents as Communication Teachers) can help improve the core challenges in social interaction and communication for children with Autism Spectrum Disorder (ASD). And to explore whether and how this intervention affects children's brain activity. We will use safe brain imaging techniques (such as MRI and functional Near-Infrared Spectroscopy, fNIRS) to compare changes in the brain before and after the intervention, aiming to understand the potential brain mechanisms behind behavioral progress. Ultimately, we hope to identify which types of children might benefit most from this intervention, providing insights for more personalized treatment recommendations in the future.
Key Questions This Study Aims to Answer:
Does participation in the IMPACT parent training program significantly improve ASD symptoms, social communication abilities, and adaptive functioning in daily life for children with ASD compared to general intervention?
Study Design:
This is a assessor blinding randomized controlled trial. Participating children will be randomly assigned to one of two groups:
IMPACT Intervention Group (approximately 40 children): The primary caregivers of these children will receive a systematic IMPACT training course over about 10 weeks (including group sessions and individual coaching), learning how to apply these techniques during interactions at home. All caregiver will be encouraged to conduct intervention at least 10 hours per week.
Control Group (approximately 40 children): The caregivers of these children will not receive IMPACT training during the initial 10-week period. They are encouraged to continue any current routine interventions their child is receiving. After 10 weeks, they will be offered the opportunity to receive the IMPACT training online for free as compensation.
Intervention Component (Exclusively for families randomly assigned to the ImPACT group):
Primary caregivers of participants will partake in the approximately 10 - week IMPACT parent training program. In weeks with odd numbers, caregivers will attend a group theory session lasting 3 - 4 hours. In weeks with even numbers, caregivers will receive a one - on - one coaching session (1 - 1.5 hours) with a trainer to enhance their intervention skills based on ImPACT. Caregivers are obligated to implement the learned strategies during daily home interactions with participants for a minimum of 10 hours per week and maintain a simple record of these activities. Trainers will monitor adherence via weekly reviews of activity logs and coaching sessions. Adherence will be further bolstered by real - time feedback during coaching sessions, where trainers prompt caregivers to engage their child in task - oriented activities while demonstrating and suggesting effective strategies, ensuring skill generalization in naturalistic settings.
The research team will evaluate all children at three time points: before the intervention starts, immediately after the 10-week intervention period, and 6 months after the intervention ends. The assessors will not know which group each child belongs to (they will be "blinded") to ensure objective results.
What the Involvement of Participation Entails:
If your child (aged 1.5 to 6.5 years) has a diagnosis of ASD and you agree to participate, the following may be involved:
Assessment Sessions (Three times: Pre-intervention, Post-intervention at 10 weeks, only SRS-2 measured after 6 months):
Questionnaires: You will be asked to fill out questionnaires about your child's behavior, social skills, and your own experiences and stress levels.
Child Assessments: A trained clinician, independent of the research team, will conduct standardized assessments of your child's development and social communication skills (e.g., ADOS-2, Griffiths Scales).
Eye-Tracking Test: Your child will watch short videos while a specialized, non-invasive device records where and for how long your child looks. This helps us understand their visual attention preferences towards social information.
Functional Near-Infrared Spectroscopy (fNIRS): During a play session, your child will wear a soft cap with sensors. It uses harmless near-infrared light to measure changes in brain activity in the outer layer of the brain. This procedure is safe, non-invasive, and radiation-free.
Magnetic Resonance Imaging (MRI) Scan (voluntary): We plan to conduct one brain MRI scan before and after the intervention for all willing participants to study brain structure and function. To ensure the child remains still during the scan, we plan to perform it during natural, deep sleep.
Voluntary Participation:
Participation in this study is completely voluntary. You may decide to withdraw yourself and your child from the study at any time, for any reason, without any penalty or effect on the future medical care you receive at this hospital or elsewhere.This study will be submitted for ethical review to ensure it meets scientific and ethical standards, protecting the rights, safety, and well-being of every participant.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| ImPACT-based Interventions | Experimental | Behavioral: Parents conducted interventions based on project ImPACT.Parent-based behavioral interventions for children. |
| General interventions | Active comparator | Behavioral: General behavioral interventionsCurrent routine interventions provided by behavioral trainers. |
Who may qualify
- Ages
- 18 to 78 months
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (4 listed)
- Participants must be between the ages of 18 months and 78 months (6.5 years) at the time of enrollment.
- Participants must have received a formal diagnosis of autism spectrum disorder (or meet criteria for conditions within the autism spectrum) from qualified clinicians, such as psychiatrists or pediatricians, in accordance with the diagnostic criteria specified in either the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) or the International Classification of Diseases, 11th Revision (ICD-11).
- Participants must have a score meeting the autism spectrum cutoff on the Autism Diagnostic Observation Schedule, Second Edition (ADOS-2).
- At least one parent is able to participate in the entire assessment and intervention procedure.
Key exclusion criteria (5 listed)
- Presence of a comorbid major neurological disorder (e.g., epilepsy, cerebral palsy) or a severe psychiatric condition.
- A history of significant brain injury or trauma.
- Current use of psychotropic medication or a within 3 months history of receiving transcranial electrical/magnetic stimulation therapy.
- Significant uncorrected impairment in visual or auditory acuity.
- Motor function disorders.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Parents conducted interventions based on project ImPACT.Also: ImPACTParents conduct behavioral interventions under the supervision of professional trainers who have obtained the certificate of Project IMPACT training. They are encouraged to conduct the interventions at least 10 hours per week without receiving other interventions from institutions or hospitals. Parents are asked to record the activities and duration of intervention they conducted daily in a logbook, which is reviewed weekly by certified trainers to ensure fidelity and provide feedback. Adherence is monitored through every other week one-one session to review progress, address challenges, and refine strategies. Trainers emphasize consistent implementation of evidence-based techniques, ensuring parents maintain high fidelity to the ImPACT model. | Behavioural | ImPACT-based Interventions |
| General behavioral interventionsChildren were subjected to interventions administered by behavioral trainers from hospitals or institutions. We advocated for them to persist with the existing interventions of any type (such as Applied Behavior Analysis, Discrete Trial Training, sensory integration, and language therapy) and augment the sessions to achieve a total of 10 hours per week, either in group or individual settings. Parents are asked to document the duration and type of sessions their children participated in each week in a notebook. | Behavioural | General interventions |
Primary outcome
Change in Autism Symptom Severity as measured by ADOS-2 Comparison Score and Subscales
Time frame: From enrollment to the end of treatment at 10 weeks.
The ADOS-2 (Autism Diagnostic Observation Schedule, Second Edition) is a semi-structured, standardized assessment of communication, social interaction, play, and restricted and repetitive behaviors. The Comparison Score is a standardized metric used to compare autism severity across different modules and ages. The Comparison Score ranges from 1 to 10, with higher scores indicating greater severity of autism spectrum-related symptoms (worse outcome).
Change in Social Impairment as measured by the Social Responsiveness Scale, Second Edition (SRS-2) Total Score
Time frame: From enrollment to the end of treatment at 10 weeks, 3months after treatment.
The SRS-2 is a 65-item caregiver-completed rating scale that measures the severity of autism spectrum symptoms as they occur in natural social settings. Each item is scored on a 4-point Likert scale ranging from 0 (Never True) to 3 (Almost Always True). The Total Raw Score is calculated by summing the scores of all 65 items. The total raw score ranges from 0 to 195, with higher scores indicating greater severity of social impairment (worse outcome).
Change in Child PFC Activation (Oxy-Hb) during Parent-Child Interaction
Time frame: From enrollment to the end of treatment at 10 weeks.
Mean Oxygenated Hemoglobin (Oxy-Hb) concentration in the Prefrontal Cortex (PFC) collected while the child engages in a standardized play task with their parent. Higher concentration indicates greater activation.
Change in Social Visual Preference Index (Percentage of Fixation Duration)
Time frame: From enrollment to the end of treatment at 10 weeks.
Participants view a battery of 3 paired paradigms presenting simultaneous social and non-social stimuli. The index is calculated as the percentage of total fixation duration spent on Social Areas of Interest (AOIs) divided by the total fixation duration on both Social and Non-social AOIs. Formula: (Duration on Social / (Duration on Social + Duration on Non-social)) * 100. The score is averaged across the 3 paradigms. Values range from 0 to 100%. Higher scores indicate a stronger preference for social stimuli.
13 secondary outcomes
Change in Adaptive Functioning as measured by the ABAS-II General Adaptive Composite (GAC) and Domain Scores
Time frame: From enrollment to the end of treatment at 10 weeks.
Change in Structural Brain Volume (Gray Matter Volume) in Regions of Interest (e.g., Prefrontal Cortex, Amygdala
Time frame: From enrollment to the end of treatment at 10 weeks.
Change in Caregiver Burden as measured by the Caregiver Strain Questionnaire (CSQ) Total Score
Time frame: From enrollment to the end of treatment at 10 weeks.
Change in Parenting Sense of Competence (PSOC): Total Score and Subscales
Time frame: From enrollment to the end of treatment at 10 weeks.
Change in Repetitive Behaviors as measured by the Repetitive Behavior Scale-Revised (RBS-R) Total Score
Time frame: From enrollment to the end of treatment at 10 weeks
Change in Social Communication Skills as measured by the Project ImPACT Social Communication Checklist (Parent-Reported)
Time frame: From enrollment to the end of treatment at 10 weeks.
ADOS-2 Raw Scores (Module 1 and Module 2)
Time frame: Baseline and Week 10
Change in Child PFC Activation (Oxy-Hb) during Interaction with Therapist
Time frame: Baseline and Week 10
Change in Child PFC Activation (Oxy-Hb) during Solitary Play
Time frame: Baseline and Week 10
Change in Social Orienting Index (Percentage of Fixation Counts)
Time frame: Baseline and Week 10.
Change in Intrinsic Functional Connectivity (Resting State fMRI)
Time frame: Baseline and Week 10
Change in Parent Intervention Fidelity as measured by the Project ImPACT Fidelity of Implementation Rating Scale
Time frame: Baseline and Week 10
Change in Social Communication Skills as measured by the Project ImPACT Social Communication Checklist (Teacher/Coach-Reported)
Time frame: Baseline and Week 10
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Feb 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Parents conducted interventions based on project ImPACT. and General behavioral interventions in people with Autism Spectrum Disorder, run by University of Electronic Science and Technology of China at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: enrolling by invitation, as of the sponsor's last update on 6 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Autism Symptom Severity as measured by ADOS-2 Comparison Score and Subscales (time frame: From enrollment to the end of treatment at 10 weeks.). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Feb 2026.