AI-assisted Home-based Intervention for ADHD Children
NCT07922018, Not applicable, Recruiting, National Taiwan University Hospital
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | AI-assisted Home-based Intervention for ADHD Children | ClinicalTrials.gov |
| NCT number | NCT07922018 | ClinicalTrials.gov |
| Status | Recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 120 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | National Taiwan University Hospital | ClinicalTrials.gov |
| Conditions | ADHD - Attention Deficit Disorder With Hyperactivity, ADHD - Combined Type, ADHD - Inattentive Type | ClinicalTrials.gov |
| Interventions | Generative artificial intelligence assisted diary platform home-based intervention, Consultations and psychoeducation on child emotional management | ClinicalTrials.gov |
| First posted | 2026-11-06 | ClinicalTrials.gov |
| Last updated | 2026-11-06 | ClinicalTrials.gov |
Registered outcomes 6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Conners CPT 3™ (The Conners Continuous Performance Test Third Edition™ ) | (1) Pre-test session to serve as baseline (2) Post-test session immediately after 12weeks | 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. | ClinicalTrials.gov |
| Primary | SNAP-IV (Swanson, Nolan, and Pelham, Version IV) | (1) Pre-test session to serve as baseline (2) Post-test session immediately after 12weeks | 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. | ClinicalTrials.gov |
| Primary | BYI-II (Beck Youth Inventories Second Edition) | (1) Pre-test session to serve as baseline (2) Post-test session immediately after 12weeks | 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. | ClinicalTrials.gov |
| Primary | CBCL Ages 6-18 (Child Behavior Checklist for Ages 6-18) | (1) Pre-test session to serve as baseline (2) Post-test session immediately after 12weeks | 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. | ClinicalTrials.gov |
| Primary | PSI (Parenting Stress Index, 3rd edition) | (1) Pre-test session to serve as baseline (2) Post-test session immediately after 12weeks | 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). | ClinicalTrials.gov |
| Primary | Parental Satisfaction Questionnaire | (1) Pre-test session to serve as baseline (2) Post-test session immediately after 12weeks | A 24-item questionnaire completed by parents or primary caregivers to understand the actual impact of this training on the child and their parents. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 13
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|---|---|
| 19301241 | BACKGROUND | PubMed |
| 22419380 | BACKGROUND | PubMed |
| 22476209 | BACKGROUND | PubMed |
| 25656314 | BACKGROUND | PubMed |
| 27435692 | BACKGROUND | PubMed |
| 29880129 | BACKGROUND | PubMed |
| 29989977 | BACKGROUND | PubMed |
| 30001717 | BACKGROUND | PubMed |
| 32063986 | BACKGROUND | PubMed |
| 32673273 | BACKGROUND | PubMed |
| 34759846 | BACKGROUND | PubMed |
| 34887721 | BACKGROUND | PubMed |
| 35015367 | BACKGROUND | PubMed |
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 1
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Continuous Performance Test | Primary outcome | ConductCognition |
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)