Effect of Game-based HIIT Program on the Executive Function of Children With ADHD
NCT05308758, Not applicable, Completed, Education University of Hong Kong
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Effect of Game-based HIIT Program on the Executive Function of Children With ADHD | ClinicalTrials.gov |
| NCT number | NCT05308758 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 47 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Education University of Hong Kong | ClinicalTrials.gov |
| Conditions | Adhd Deficits in Attention Motor Control and Perception | ClinicalTrials.gov |
| Interventions | Game-based High-Intensity Interval Training, GameSAE | ClinicalTrials.gov |
| First posted | 2022-04-04 | ClinicalTrials.gov |
| Last updated | 2025-08-08 | ClinicalTrials.gov |
Registered outcomes 55
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Colour-Word Stroop Test (CWST) | The measurements are assessed at baseline (T0). | The executive function will be assessed using a battery of tests on a laptop computer that will take approximately five minutes to complete. The battery of tests include the Colour-Word Stroop Test (CWST), Corsi Block Tapping Test (CBTT), Wisconsin Card Sorting Test (WCST), and Tower of London Test (TLT) which are classic tasks that measure inhibition response, one of important components of executive function. | ClinicalTrials.gov |
| Primary | Corsi Block Tapping Test (CBTT) | The measurements are assessed at baseline (T0). | Executive function will be assessed using a battery of tests on a laptop computer that will take approximately five minutes to complete. The battery of tests include the Colour-Word Stroop Test (CWST), Corsi Block Tapping Test (CBTT), Wisconsin Card Sorting Test (WCST), and Tower of London Test (TLT) which are classic tasks that measure inhibition response, one of important components of executive function. | ClinicalTrials.gov |
| Primary | Wisconsin Card Sorting Test (WCST) | The measurements are assessed at baseline (T0). | The executive function will be assessed using a battery of tests on a laptop computer that will take approximately five minutes to complete. The battery of tests include the Colour-Word Stroop Test (CWST), Corsi Block Tapping Test (CBTT), Wisconsin Card Sorting Test (WCST), and Tower of London Test (TLT) which are classic tasks that measure inhibition response, one of the important components of executive function. | ClinicalTrials.gov |
| Primary | Tower of London Test (TLT) | The measurements are assessed at baseline (T0). | Executive function will be assessed using a battery of tests on a laptop computer that will take approximately five minutes to complete. The battery of tests include the Colour-Word Stroop Test (CWST), Corsi Block Tapping Test (CBTT), Wisconsin Card Sorting Test (WCST), and Tower of London Test (TLT) which are classic tasks that measure inhibition response, one of important components of executive function. | ClinicalTrials.gov |
| Primary | Colour-Word Stroop Test (CWST) | The measurements are assessed after the 8-week intervention period (T1). | Executive function will be assessed using a battery of tests on a laptop computer that will take approximately five minutes to complete. The battery of tests include the Colour-Word Stroop Test (CWST), Corsi Block Tapping Test (CBTT), Wisconsin Card Sorting Test (WCST), and Tower of London Test (TLT) which are classic tasks that measure inhibition response, one of important components of executive function. | ClinicalTrials.gov |
| Primary | Corsi Block Tapping Test (CBTT) | The measurements are assessed after the 8-week intervention period (T1). | Executive function will be assessed using a battery of tests on a laptop computer that will take approximately five minutes to complete. The battery of tests include the Colour-Word Stroop Test (CWST), Corsi Block Tapping Test (CBTT), Wisconsin Card Sorting Test (WCST), and Tower of London Test (TLT) which are classic tasks that measure inhibition response, one of important components of executive function. | ClinicalTrials.gov |
| Primary | Wisconsin Card Sorting Test (WCST) | The measurements are assessed after the 8-week intervention period (T1). | Executive function will be assessed using a battery of tests on a laptop computer that will take approximately five minutes to complete. The battery of tests include the Colour-Word Stroop Test (CWST), Corsi Block Tapping Test (CBTT), Wisconsin Card Sorting Test (WCST), and Tower of London Test (TLT) which are classic tasks that measure inhibition response, one of important components of executive function. | ClinicalTrials.gov |
| Primary | Tower of London Test (TLT) | The measurements are assessed after the 8-week intervention period (T1). | Executive function will be assessed using a battery of tests on a laptop computer that will take approximately five minutes to complete. The battery of tests include the Colour-Word Stroop Test (CWST), Corsi Block Tapping Test (CBTT), Wisconsin Card Sorting Test (WCST), and Tower of London Test (TLT) which are classic tasks that measure inhibition response, one of important components of executive function. | ClinicalTrials.gov |
| Primary | Colour-Word Stroop Test (CWST) | The measurements are assessed after the 8-week intervention period, as well as another 8-week follow up (T2). | Executive function will be assessed using a battery of tests on a laptop computer that will take approximately five minutes to complete. The battery of tests include the Colour-Word Stroop Test (CWST), Corsi Block Tapping Test (CBTT), Wisconsin Card Sorting Test (WCST), and Tower of London Test (TLT) which are classic tasks that measure inhibition response, one of important components of executive function. | ClinicalTrials.gov |
| Primary | Corsi Block Tapping Test (CBTT) | The measurements are assessed after the 8-week intervention period, as well as another 8-week follow up (T2). | Executive function will be assessed using a battery of tests on a laptop computer that will take approximately five minutes to complete. The battery of tests include the Colour-Word Stroop Test (CWST), Corsi Block Tapping Test (CBTT), Wisconsin Card Sorting Test (WCST), and Tower of London Test (TLT) which are classic tasks that measure inhibition response, one of important components of executive function. | ClinicalTrials.gov |
| Primary | Wisconsin Card Sorting Test (WCST) | The measurements are assessed after the 8-week intervention period, as well as another 8-week follow up (T2). | Executive function will be assessed using a battery of tests on a laptop computer that will take approximately five minutes to complete. The battery of tests include the Colour-Word Stroop Test (CWST), Corsi Block Tapping Test (CBTT), Wisconsin Card Sorting Test (WCST), and Tower of London Test (TLT) which are classic tasks that measure inhibition response, one of important components of executive function. | ClinicalTrials.gov |
| Primary | Tower of London Test (TLT) | The measurements are assessed after the 8-week intervention period, as well as another 8-week follow up (T2). | Executive function will be assessed using a battery of tests on a laptop computer that will take approximately five minutes to complete. The battery of tests include the Colour-Word Stroop Test (CWST), Corsi Block Tapping Test (CBTT), Wisconsin Card Sorting Test (WCST), and Tower of London Test (TLT) which are classic tasks that measure inhibition response, one of important components of executive function. | ClinicalTrials.gov |
| Primary | Cerebral Hemodynamic Response | The measurements are assessed at baseline (T0). | Accompanied by the executive function test, the cortical hemodynamic response in the prefrontal cortex will also be recorded using a multi-channel fNIRS (Octamon fNIRS system, Artinis, Netherland) applying two wavelengths of near-infrared light (785 and 830 nm). The device consists of eight light sources and two detectors secured onto a head cap. The device will be placed over the left and right prefrontal cortex according to the guidelines in the handbook provided by the manufacturer. | ClinicalTrials.gov |
| Primary | Cerebral Hemodynamic Response | The measurements are assessed after the 8-week intervention period (T1). | Accompanied by the executive function test, the cortical hemodynamic response in the prefrontal cortex will also be recorded using a multi-channel fNIRS (Octamon fNIRS system, Artinis, Netherland) applying two wavelengths of near-infrared light (785 and 830 nm). The device consists of eight light sources and two detectors secured onto a head cap. The device will be placed over the left and right prefrontal cortex according to the guidelines in the handbook provided by the manufacturer. | ClinicalTrials.gov |
| Primary | Cerebral Hemodynamic Response | The measurements are assessed after the 8-week intervention period, as well as another 8-week follow up (T2). | Accompanied by the executive function test, the cortical hemodynamic response in the prefrontal cortex will also be recorded using a multi-channel fNIRS (Octamon fNIRS system, Artinis, Netherland) applying two wavelengths of near-infrared light (785 and 830 nm). The device consists of eight light sources and two detectors secured onto a head cap. The device will be placed over the left and right prefrontal cortex according to the guidelines in the handbook provided by the manufacturer. | ClinicalTrials.gov |
| Secondary | Body height | The measurements are assessed at baseline (T0). | Body height will be measured in meters. The measurement will follow the Anthropometry Procedures Manual of the National Health and Nutrition Examination Survey (NHANES). Weight and height will be combined to report BMI in kg/m\^2. | ClinicalTrials.gov |
| Secondary | Body height | The measurements are assessed after the 8-week intervention period (T1). | Body height will be measured in meters. The measurement will follow the Anthropometry Procedures Manual of the National Health and Nutrition Examination Survey (NHANES). Weight and height will be combined to report BMI in kg/m\^2. | ClinicalTrials.gov |
| Secondary | Body height | The measurements are assessed after the 8-week intervention period, as well as another 8-week follow up (T2). | Body height will be measured in meters. The measurement will follow the Anthropometry Procedures Manual of the National Health and Nutrition Examination Survey (NHANES). Weight and height will be combined to report BMI in kg/m\^2. | ClinicalTrials.gov |
| Secondary | Body weight | The measurements are assessed at baseline (T0). | Bodyweight will be measured in kilograms. The measurement will follow the Anthropometry Procedures Manual of the National Health and Nutrition Examination Survey (NHANES). Weight and height will be combined to report BMI in kg/m\^2. | ClinicalTrials.gov |
| Secondary | Body weight | The measurements are assessed after the 8-week intervention period (T1). | Bodyweight will be measured in kilograms. The measurement will follow the Anthropometry Procedures Manual of the National Health and Nutrition Examination Survey (NHANES). Weight and height will be combined to report BMI in kg/m\^2. | 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 45
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|---|---|
| 7893421 | BACKGROUND | PubMed |
| 8655658 | BACKGROUND | PubMed |
| 11322578 | BACKGROUND | PubMed |
| 12086747 | BACKGROUND | PubMed |
| 12638061 | BACKGROUND | PubMed |
| 14962399 | BACKGROUND | PubMed |
| 15334986 | BACKGROUND | PubMed |
| 15370482 | BACKGROUND | PubMed |
| 16253636 | BACKGROUND | PubMed |
| 16421041 | BACKGROUND | PubMed |
| 16492261 | BACKGROUND | PubMed |
| 16794878 | BACKGROUND | PubMed |
| 17541055 | BACKGROUND | PubMed |
| 18094706 | BACKGROUND | PubMed |
| 20161467 | BACKGROUND | PubMed |
| 20459784 | BACKGROUND | PubMed |
| 20586996 | BACKGROUND | PubMed |
| 20837978 | BACKGROUND | PubMed |
| 21262822 | BACKGROUND | PubMed |
| 21814148 | 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 4
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 |
|---|---|---|
| Card Sorting Test (Berg) | Primary outcome | ConductCognition |
| Corsi Block-Tapping Test | Primary outcome | ConductCognition |
| Stroop Color-Word Test | Primary outcome | ConductCognition |
| Tower Planning | 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)