Neurofeedback-Based Digital Therapeutics for the Diagnosis and Treatment of ADHD in Children.
- Conditions
- Attention Deficit Disorder with HyperactivityExecutive Function Disorder
- Interventions
- Device: Digital therapeutics
- Registration Number
- NCT06369714
- Lead Sponsor
- Lei Lei, MD
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 200
- 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.
- 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.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Medication group Concerta The medication group will take Methylphenidate Hydrochloride Extended-Release Tablets with a fixed dose for eight weeks. Digital therapeutics group Digital therapeutics The digital therapeutics group will complete 30 training sessions within 8 weeks. Combination group Concerta The combination group will take Methylphenidate Hydrochloride Extended-Release Tablets while undergoing digital therapeutics. Combination group Digital therapeutics The combination group will take Methylphenidate Hydrochloride Extended-Release Tablets while undergoing digital therapeutics.
- Primary Outcome Measures
Name Time Method Swanson, Nolan, and Pelham IV Rating Scale Baseline 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 Outcome Measures
Name Time Method Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition criteria for ADHD Baseline 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 Difficulties Baseline 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 Function Baseline 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 Test Baseline 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 Test Baseline 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.
Trial Locations
- Locations (2)
Changzheng Hospital, Naval Medical University
🇨🇳Shanghai, Shanghai, China
Changhai Hospital, Naval Medical University
🇨🇳Shanghai, Shanghai, China