Temporal Pole Transcranial Alternating Current Stimulation for Children With Autism Spectrum Disorder

Fei Li

Status: Active, not recruiting

Conditions: Autism Spectrum Disorder

Treatments: Device: transcranial Temporal Interference Stimulation; Device: Transcranial Alternating Current Stimulation

Study type: Interventional

Funder types: Other

Identifiers

NCT07045584

XHEC-C-2025-090-3

Details and patient eligibility

About

The goal of this open-label randomized controlledl trial is to explore the safety and efficacy of conventional transcranial alternating current stimulation (tACS) and transcranial temporal interference stimulation (tTIS) targeting the temporal pole in children with autism spectrum disorder (ASD) in China. The main questions it aims to answer are:

*Can tACS and tTIS safely and effectively improve clinical symptoms in children with autism?

Researchers will compare the tACS group and tTIS group with control group to explore the safety, feasibility and efficacy of the transcranial electrical stimulation in children with autism.

Participants will:

• tACS group: undergo 5 days of temporal pole tACS
• tTIS group:undergo 5 days of temporal pole tTIS
• Control group: receive routine rehabilitation training during the study period.

From baseline to 4 weeks after intervention completion, subjects will be followed up regarding clinical symptoms and adverse reactions:

• Safety Outcome Measures: adverse events
• Primary Efficacy Outcome Measures: Social Responsiveness Scale (SRS-2) total scores
• Other clinical outcome measures related language, adapative function and cognition

Full description

This research is a 5-week prospective, open-label, randomized controlled trial, planning to enroll 36 autistic children aged 4-10 with a full-scale intelligence quotient (FSIQ) of 50 or above. Children who satisfy all inclusion criteria without meeting any exclusion criteria, may be enrolled after their legal guardians provided the written informed consent.

Eligible subjects will be randomly divided into three groups: tACS group, tTIS group and control group. The tACS group will undergo 5 days of temporal pole tACS stimulation (1.5mA, 40Hz, 20min/session, 6 sessions/day); the tTIS group will undergo 5 days of temporal pole TI stimulation（1.5mA, 2040/2000Hz, 20min/session, 6 sessions/day）; the control group will receive routine rehabilitation training during the study period, including various rehabilitation services provided by the community.

At baseline, subjects will undergo physical measurements, demographic and medical history collection, intelligence test and symptom clinical scale assessments, and resting-state EEG collection. From the start of intervention until 4 weeks after completion, subjects will be followed up regarding clinical symptoms, neuroimaging, and adverse reactions.

The safety outcome: adverse events and their rate. The primary efficacy outcome is the change in Social Responsiveness Scale (SRS-2) scores 4 weeks after intervention completion compared to pre-intervention.

Secondary outcomes include changes in SRS-2 scores immediately after the 5-day intervention compared to pre-intervention; and changes in Chinese Communicative Development Inventory (CCDI), Childhood Autism Rating Scale (CARS), Peabody Picture Vocabulary Test (PPVT), Developmental Neuropsychological Assessment (NEPSY-II, including narrative memory, facial memory, theory of mind, vocabulary generation) four items, and Clinical Global Impression (CGI) scale scores 4 weeks after the 5-day intervention compared to pre-intervention.

Exploratory indicators include changes in resting-state EEG neuroimaging characteristics before intervention, immediately after the 5-day intervention, and 4 weeks after the 5-day intervention.

Enrollment: 36 estimated patients

Sex: All

Ages: 4 to 10 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Children aged 4-10 years
2. Meeting the diagnostic criteria for ASD according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5)
3. Diagnosis confirmed by the Autism Diagnostic Observation Schedule (ADOS) and/or the Autism Diagnostic Interview-Revised (ADI-R)
4. Full Scale Intelligence Quotient (FSIQ) ≥50
5. Signed informed consent form

Exclusion criteria

1. Individuals with metal implants in the body
2. Individuals with neurological disorders such as epilepsy
3. Those requiring surgical treatment due to structural abnormalities indicated by brain MRI examination
4. Those diagnosed with genetic or chromosomal abnormalities
5. Individuals with mental illness (such as mood disorders, etc.)
6. Those with severe cardiac disease
7. Individuals with increased intracranial pressure
8. Those currently participating in other clinical trials
9. Those who received new intervention protocols within 4 weeks prior to enrollment.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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36 participants in 3 patient groups

Intervention group(tACS)

Experimental group

Description:

Receive tACS stimulation targeting the temporal pole, with stimulation frequency of 40Hz, using adapter power supply: voltage 9V, current set at 1.5mA, 6 times/day, 20min/session with 20min intervals between sessions, lasting for 5 days

Treatment:

Device: Transcranial Alternating Current Stimulation

Control group

No Intervention group

Description:

Receive routine rehabilitation training during the study period

Intervention group(tTIS)

Experimental group

Description:

Receive tTIS targeting the temporal pole, with stimulation frequency of 2040/2000HZ, using battery power supply: voltage 12V, current set at 1.5mA, 6 times/day, 20min/session with 20min intervals between sessions, lasting for 5 days

Treatment:

Device: transcranial Temporal Interference Stimulation