An interventional study of Generative artificial intelligence assisted diary platform home-based intervention and Consultations and psychoeducation on child emotional management in ADHD - Attention Deficit Disorder With Hyperactivity, ADHD - Combined Type and ADHD - Inattentive Type, sponsored by National Taiwan University Hospital. Recruiting at 1 site in Taiwan. Open to participants aged 8 Years to 12 Years. Per ClinicalTrials.gov, last updated 2026-11-06.
Sponsored by National Taiwan University Hospital · Not applicable, Interventional, and Treatment
The goal of this clinical trial is to evaluate the effectiveness of online diary platforms for socio-emotional learning training in children with attention deficit hyperactivity disorder (ADHD). The main questions it aims to answer are:
Does the online diary platform training enhance children's emotion regulation and its connection to positive thinking? Does the online diary platform training provide an immediate, interactive, and effective emotion training tool during the wait for follow-up visits and treatment?
Researchers will compare online diary platforms training to counselling to see if online diary platforms training enhance children's emotion regulation.
Participants will use the MangaChat diary platform to log their daily moods and events, which the platform transforms into comic strips to offer an engaging visual story of their emotional experiences. Participants are requested to use the platform daily (or at least 3 times per week) for approximately 10 to 15 minutes per session over a 12-week period.
1,817 studies on the registry are indexed under Attention Deficit Disorder with Hyperactivity; 296 are open to participants now.
This study's planned enrollment of 120 is above the median of 71 across 1,437 interventional studies indexed under Attention Deficit Disorder with Hyperactivity.
Browse Attention Deficit Disorder with Hyperactivity studies →National Taiwan University Hospital is the lead sponsor of 2,615 studies on the registry; 576 are open to participants now.
Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Intellectual disability, defined as a Full Scale Intelligence Quotient (FSIQ) score of less than 70.
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Device: Generative artificial intelligence assisted diary platform home-based intervention
Behavioral: Consultations and psychoeducation on child emotional management
Participants will use the MangaChat diary platform to log their daily moods and events, which the platform transforms into comic strips to offer an engaging visual story of their emotional experiences. Participants are requested to use the platform daily (or at least 3 times per week) for approximately 10 to 15 minutes per session over a 12-week period. Prior to using the platform, a 1-hour online orientation session will be provided to guide parents on how to support their child's emotional management at home using the digital tool.
A clinical psychologist will provide weekly 30-minute telephone consultations and psychoeducation for parents on child emotional management over a 12-week period. These sessions will focus on discussing real-life situations and establishing coping strategies. (If parents express interest in using the online platform, free access equivalent to the 12-week intervention given to the platform group will be provided after study completion, ensuring their rights and benefits are fully preserved regardless of group assignment.)
Conners CPT 3™ (The Conners Continuous Performance Test Third Edition™ )
A 14-minute, computerized visual attention assessment that evaluates objective performance to assist in the assessment of ADHD. The test evaluates performance across four primary dimensions: inattentiveness, impulsivity, sustained attention an vigilance.
Time frame: (1) Pre-test session to serve as baseline (2) Post-test session immediately after 12weeks
SNAP-IV (Swanson, Nolan, and Pelham, Version IV)
A 26-Item standardized behavior rating scale completed by parents to compare a child's behavior across home and school environments. This scale evaluates inattention, hyperactivity/impulsivity, oppositional defiant/conduct behaviors.
Time frame: (1) Pre-test session to serve as baseline (2) Post-test session immediately after 12weeks
BYI-II (Beck Youth Inventories Second Edition)
A standardized psychological assessment designed to evaluate emotional and social impairment in children and adolescents, completed by parents. The BYI-II consists of 100 total items, assesses symptoms of depression, anxiety, anger, disruptive behavior, and self-concept.
Time frame: (1) Pre-test session to serve as baseline (2) Post-test session immediately after 12weeks
CBCL Ages 6-18 (Child Behavior Checklist for Ages 6-18)
A standardized questionnaire completed by parents or primary caregivers to evaluate a child's behavioral, emotional, and social functioning over the past 6 months. The questionnaire is divided into competence Items , measures the child's active participation and performance, and problem Items , evaluates emotional and behavioral difficulties, yielding several key groups of scales, including anxious/depressed, withdrawn/depressed, somatic complaints, social problems, thought problems, attention problems, rule-breaking behavior and aggressive behavior.
Time frame: (1) Pre-test session to serve as baseline (2) Post-test session immediately after 12weeks
PSI (Parenting Stress Index, 3rd edition)
A questionnaire designed to measure the relative magnitude of stress in the parent-child system for parents of children, completed by parents or primary caregivers to. Consists of 120 items on a 5-point Likert scale divided into two main domains plus an optional life stress measure: 1. Child domain (47 items): Evaluates child characteristics across six subscales: * Distractibility/Hyperactivity * Adaptability * Reinforces Parent * Demandingness * Mood * Acceptability (of the child to the parent) 2. Parent Domain (54 items): Evaluates parental characteristics across seven subscales: * Competence * Isolation * Attachment * Health * Role Restriction * Depression * Spouse (relationship with spouse/partner) 3. Life Stressors Domain (Optional, 19 items): Measures extraneous/situational life events (e.g., job loss, financial hardship, family moves).
Time frame: (1) Pre-test session to serve as baseline (2) Post-test session immediately after 12weeks
Parental Satisfaction Questionnaire
A 24-item questionnaire completed by parents or primary caregivers to understand the actual impact of this training on the child and their parents.
Time frame: (1) Pre-test session to serve as baseline (2) Post-test session immediately after 12weeks
Plan to share: No
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
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