Attention Deficit Hyperactivity Disorder (ADHD)NCT06950866
Home-Based Executive Function Training Intervention For Attention-Deficit/ Hyperactivity Disorder-prone Children
A study testing Home-based executive function training therapy in people with Attention Deficit Hyperactivity Disorder (ADHD), run by Wuhan Mental Health Centre.
Trial summary
This study aims to investigate the effectiveness of a home-based executive function training Intervention on children's ADHD symptoms, executive function and parents' parenting stress. Read more about this study
- Who is it for?
- Ages 6 to 12 years
- Conditions the study is for
- Attention Deficit Hyperactivity Disorder (ADHD)
- What is being tested?
- Home-based executive function training therapy
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- No sites listed yet
- Study dates
- 1 May 2025to 1 Sep 2025
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 6 to 12 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- 1.SNAP-IV scale, inattention or hyperactivity-impulsivity scale score > 1.2
- 2.Parents who could understand or lacking of access to computers and the Internet
- 3.Parents can commit to ensuring full participation and complete the training and test evaluations in full compliance with the researcher's requirements
- 4.Children and their parents consent to the study
Who cannot join
- 1.Children or parents with severe organic encephalopathy and other severe mental disorders
- 2.Parents or children are receiving ADHD-related behavioral treatment
- 3.Parents or children who dropped out before the study started or in the middle of the study
About this study
This study aims to investigate the effectiveness of a home-based executive function training Intervention on children's ADHD symptoms, executive function and parents' parenting stress.
- Being tested
- Home-based executive function training therapy
- Keywords
- Attention Deficit Hyperactivity Disorder (ADHD), Executive function training
- Medical subject headings
- Attention Deficit Disorder with Hyperactivity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Home-based executive function training therapyBehavioural
Parents receive a 2-week, 20-session online child executive function training program, delivered by a systematically trained and supervised therapist.
Home-based executive function training therapyBehavioural
After the postintervention data collection, parents in the waitlist group receive a 2-week, 20-session online child executive function training program, delivered by a systematically trained and supervised therapist.
| Study group | Role | What they receive |
|---|---|---|
| Intervention group | Experimental | Not described Receives: Behavioral: Home-based executive function training therapy |
| Waitlist group | Other | Not described Receives: Behavioral: Home-based executive function training therapy |
What is being measured
The primary outcome is the main question the study is designed to answer.
1.Chinese version of Swan-son Nolan and Pelham, Version IV Scale-parent form (SNAP-IV)
This questionnaire is used to evaluate the children's ADHD symptoms.
Measured: Baseline, 1 month after intervention, 2 months after intervention
2.Behavior Rating Inventory of Executive Function (BRIEF)
This questionnaire is used to evaluate the children's executive function.
Measured: Baseline, 1 month after intervention, 2 months after intervention
3.Parenting Stress Index-Short Form (PSI-SF)
This questionnaire is used to evaluate the parents' parenting stress.
Measured: Baseline, 1 month after intervention, 2 months after intervention
Secondary outcomes (1)
4.Client Satisfaction Questionnaire (CSQ)
This questionnaire is used to evaluate the parents' satisfaction with the intervention.
Measured: Baseline, 1 month after intervention, 2 months after intervention
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Apr 2025
- Study start1 May 2025 (estimated)
- Primary completion1 Sep 2025 (estimated)
- Study completion1 Sep 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Attention Deficit Hyperactivity Disorder (ADHD)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Wuhan Mental Health Centre
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06950866
- Sponsor's protocol ID
- KY2024.0710.15
- Status last verified
- Apr 2025
- First submitted
- 22 Apr 2025
- Last updated
- 30 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 30 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Home-Based Executive Function Training Intervention For Attention-Deficit/ Hyperactivity Disorder-prone Children
- ClinicalTrials.gov ID
- NCT06950866
- Acronym / sponsor ID
- KY2024.0710.15
- Keywords
- Attention Deficit Hyperactivity Disorder (ADHD), Executive function training
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Wuhan Mental Health CentreUniversity, hospital or other
- Study start
- 1 May 2025 (estimated)
- Primary completion
- 1 Sep 2025 (estimated)
- Study completion
- 1 Sep 2025 (estimated)
- First posted
- 30 Apr 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study aims to investigate the effectiveness of a home-based executive function training Intervention on children's ADHD symptoms, executive function and parents' parenting stress.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention group | Experimental | Behavioral: Home-based executive function training therapy |
| Waitlist group | Other | Behavioral: Home-based executive function training therapy |
Who may qualify
- Ages
- 6 to 12 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (4 listed)
- 1.SNAP-IV scale, inattention or hyperactivity-impulsivity scale score > 1.2
- 2.Parents who could understand or lacking of access to computers and the Internet
- 3.Parents can commit to ensuring full participation and complete the training and test evaluations in full compliance with the researcher's requirements
- 4.Children and their parents consent to the study
Key exclusion criteria (3 listed)
- 1.Children or parents with severe organic encephalopathy and other severe mental disorders
- 2.Parents or children are receiving ADHD-related behavioral treatment
- 3.Parents or children who dropped out before the study started or in the middle of the study
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Home-based executive function training therapyParents receive a 2-week, 20-session online child executive function training program, delivered by a systematically trained and supervised therapist. | Behavioural | Intervention group |
| Home-based executive function training therapyAfter the postintervention data collection, parents in the waitlist group receive a 2-week, 20-session online child executive function training program, delivered by a systematically trained and supervised therapist. | Behavioural | Waitlist group |
Primary outcome
1.Chinese version of Swan-son Nolan and Pelham, Version IV Scale-parent form (SNAP-IV)
Time frame: Baseline, 1 month after intervention, 2 months after intervention
This questionnaire is used to evaluate the children's ADHD symptoms.
2.Behavior Rating Inventory of Executive Function (BRIEF)
Time frame: Baseline, 1 month after intervention, 2 months after intervention
This questionnaire is used to evaluate the children's executive function.
3.Parenting Stress Index-Short Form (PSI-SF)
Time frame: Baseline, 1 month after intervention, 2 months after intervention
This questionnaire is used to evaluate the parents' parenting stress.
1 secondary outcome
4.Client Satisfaction Questionnaire (CSQ)
Time frame: Baseline, 1 month after intervention, 2 months after intervention
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Apr 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
A study testing Home-based executive function training therapy in people with Attention Deficit Hyperactivity Disorder (ADHD), run by Wuhan Mental Health Centre.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 30 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
1.Chinese version of Swan-son Nolan and Pelham, Version IV Scale-parent form (SNAP-IV) (time frame: Baseline, 1 month after intervention, 2 months after intervention). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Apr 2025.