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Neurofeedback-Based Digital Therapeutics for the Diagnosis and Treatment of ADHD in Children.

Neurofeedback-Based Digital Therapeutics for the Diagnosis and Treatment of Attention Deficit Hyperactivity Disorder (ADHD) in Children.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06369714
Acronym
ADHD
Enrollment
210
Registered
2024-04-17
Start date
2023-02-24
Completion date
2025-12-31
Last updated
2025-06-10

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

Conditions

Attention Deficit Disorder With Hyperactivity, Executive Function Disorder

Keywords

Digital Therapeutics, Neurofeedback, Attention Deficit Disorders with Hyperactivity, Children, Executive function disorder

Brief summary

A multi-center, randomized controlled trial is being conducted to investigate the efficacy of a novel digital therapeutics (DTx) program that utilizes a cross-training approach between neurofeedback training and executive function training for pediatric patients (aged 6-12) diagnosed with ADHD. This gamified interactive program is designed to improve attention deficits and executive function impairments in pediatric patients with ADHD. It is delivered through an engaging iPad game in a home-based treatment format. Patients will be randomly assigned to one of three groups: medication alone, digital therapeutics alone, or a combination of both interventions. Subjects will undergo 30 treatment sessions over the 8-week period, with each session lasting 30 minutes. Investigators will reassess symptoms of ADHD, executive functions, and objective measures of attention at the end of the treatment. Additionally, questionnaires will be distributed to parents to gather their insights and feedback on the treatment approach. This innovative digital therapeutics approach is expected to improve ADHD symptoms individually and enhance therapeutic outcomes when used alongside conventional drug treatment regimens.

Interventions

Methylphenidate Hydrochloride Extended-Release Tablets with the following specifications: 18mg dosage, oral administration, once a day for a duration of 8 weeks.

30 sessions of digital therapeutics, each lasting 30 minutes, will be conducted with a frequency of once every 1-2 days over an 8-week period.

Sponsors

Lei Lei, MD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Meet the diagnostic criteria established by the 5th edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) for ADHD. * Digital Cancellation Test total score\<50 points. * Raven's Standard Progressive Matrices score≥85. * 6 years ≤ Age\<12 years. * No interventions for ADHD received within 4 weeks. * No color blindness.

Exclusion criteria

* Patients with organic mental disorders, schizophrenia, bipolar disorder, depressive disorders, and other psychiatric conditions. * Patients with comorbid autism spectrum disorder, Tourette's syndrome, and other neurodevelopmental disorders. * Patients with comorbid conduct disorders. * Patients with severe traumatic brain injury or neurological disorders. * Patients with a history of severe somatic diseases. * Patients with a history of substance or drug dependency.

Design outcomes

Primary

MeasureTime frameDescription
Swanson, Nolan, and Pelham IV Rating ScaleBaseline to End of Treatment (Week 8) and to Follow-up (Week 20, Week 32)The Swanson, Nolan, and Pelham IV Rating Scales (SNAP-IV) will be completed by parents to assess the severity of ADHD symptoms. The values range from 0 to 3, with lower scores indicating a better outcome.

Secondary

MeasureTime frameDescription
Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition criteria for ADHDBaseline to End of Treatment (Week 8) and to Follow-up (Week 20, Week 32)The Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria for ADHD will be used to assess the number of core symptoms. There are a total of 18 core symptoms, with fewer symptoms indicating a better outcome.
Questionnaire-Children with DifficultiesBaseline to End of Treatment (Week 8) and to Follow-up (Week 20, Week 32)The Questionnaire-Children with Difficulties (QCD) will be completed by parents to assess the social abilities of participants. The total questionnaire score is 57, and a score below 30 suggests impaired functioning.
Behavior Rating Inventory of Executive FunctionBaseline to End of Treatment (Week 8) and to Follow-up (Week 20, Week 32)The Behavior Rating Inventory of Executive Function (BRIEF) will be completed by parents to assess changes in executive function. The normal standards for scores vary by age, with lower scores indicating a better outcome.
Continuous Performance TestBaseline to End of Treatment (Week 8) and to Follow-up (Week 20, Week 32)A newly designed Continuous Performance Test (CPT) will be administered to participants by investigators, with higher accuracy rates indicating a better outcome.
Digital Cancellation TestBaseline to End of Treatment (Week 8) and to Follow-up (Week 20, Week 32)The Digit Cancellation Test (DCT) will be administered to participants by investigators, with higher scores indicating a better outcome.

Countries

China

Contacts

Primary ContactYuanhao Cai, MBBS
15552283399@163.com15001969690
Backup ContactLei Lei, MD
doctorlei_lei@163.com13916072205

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026