CogniFit Computerized Cognitive Training in Primary School Students in Hong Kong
The Effects of Computerized Cognitive Training on Executive Function in Children in Hong Kong
1 other identifier
interventional
176
1 country
1
Brief Summary
This study aims to address these gaps by conducting a comprehensive evaluation of the effects of CogniFit training in children. The primary objective of this study is to evaluate the effectiveness of CogniFit training on executive functions among primary school students in Hong Kong. Specific objectives include:
- 1.To assess the effectiveness of CogniFit training on improving executive functions, such as working memory, attention, and inhibitory control in children compared to a waitlist control group.
- 2.To assess the effectiveness of CogniFit training on improving executive functions, such as working memory, attention, and inhibitory control in children compared to an active control group that will receive Cogmed training.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Dec 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2024
CompletedFirst Submitted
Initial submission to the registry
January 3, 2025
CompletedFirst Posted
Study publicly available on registry
January 9, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 23, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 23, 2025
CompletedApril 29, 2026
April 1, 2026
1.1 years
January 3, 2025
April 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (6)
Executive Functiong - Conners Continuous Performance Test 3rd Edition (CPT 3)
A standardized computerized test on sustained attention and inhibitory control
Pre-intervention Assessment (within 4 weeks before the commencement of the intervention)
Executive Functiong - Conners Continuous Performance Test 3rd Edition (CPT 3)
A standardized computerized test on sustained attention and inhibitory control
Immediate Post-intervention Assessment (within 4 weeks after the completion of the intervention)
Executive Functiong - Conners Continuous Performance Test 3rd Edition (CPT 3)
A standardized computerized test on sustained attention and inhibitory control
Delayed Post-intervention Assessment (a 2-month follow up after the completion of the intervention)
Executive Function - Number subtest of Children's Memory Scale (CMS)
A verbal working memory test using digit span, with a higher score indicating a higher level of verbal working memory. The total score of this test ranges from 0 to 30.
Pre-intervention Assessment (within 4 weeks before the commencement of the intervention)
Executive Function - Number subtest of Children's Memory Scale (CMS)
A verbal working memory test using digit span, with a higher score indicating a higher level of verbal working memory. The total score of this test ranges from 0 to 30.
Immediate Post-intervention Assessment (within 4 weeks after the completion of the intervention)
Executive Function - Number subtest of Children's Memory Scale (CMS)
A verbal working memory test using digit span, with a higher score indicating a higher level of verbal working memory. The total score of this test ranges from 0 to 30.
Delayed Post-intervention Assessment (a 2-month follow up after the completion of the intervention)
Secondary Outcomes (3)
Behavioural ratings on children's executive functions
Pre-intervention Assessment (within 4 weeks before the commencement of the intervention)
Behavioural ratings on children's executive functions
Immediate Post-intervention Assessment (within 4 weeks after the completion of the intervention)
Behavioural ratings on children's executive functions
Delayed Post-intervention Assessment (a 2-month follow up after the completion of the intervention)
Study Arms (3)
CogniFit Group
EXPERIMENTALThe CogniFit training group will receive 24 sessions of training, 35 - 40 minutes each, conducted three times per week over a period of 8 weeks. Participants will be asked to complete a set of computerized tasks using CogniFit, a digital training programme which is proven to enhance cognitive ability of participants.
Cogmed Group
ACTIVE COMPARATORThe Cogmed training group will receive 24 sessions of training, 35 - 40 minutes each, conducted three times per week over a period of 8 weeks. Participants will be asked to complete a set of computerized tasks using Cogmed, a digital training programme which is proven to enhance working memory and attentional control of participants.
Waitlist Control Group
NO INTERVENTIONThe waitlist control group will not receive any intervention until the intervention arms complete their training. After completion of the assessment at Timepoint 3, Computerized Cognitive Training will be offered to this group.
Interventions
In the CogniFit Computerized Cognitive Training, children will complete a range of tasks covering a range of game-like exercises targeting various cognitive skills, including working memory, attention, and inhibitory control, with automatic level advancement after each exercise.
In the Cogmed Computerized Cognitive Training, children will complete a range of tasks covering a range of game-like exercises targeting various cognitive skills, including working memory and attentional control, with automatic level advancement after each exercise.
Eligibility Criteria
You may qualify if:
- Children aged 6- 12
- Studying in Grade 1 to 6 in mainstream primary schools in Hong Kong
You may not qualify if:
- Inability to answer the first five questions in Raven's Progressive Matrices
- Hearing, visual, or physical impairments that might hinder participation in the training and assessment activities
- Current participation in a computerized cognitive treatment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- The University of Hong Konglead
- Edge Development Centrecollaborator
Study Sites (1)
The University of Hong Kong
Hong Kong, Hong Kong
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
January 3, 2025
First Posted
January 9, 2025
Study Start
December 1, 2024
Primary Completion
December 23, 2025
Study Completion
December 23, 2025
Last Updated
April 29, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will share
- Time Frame
- Beginning immediately after publication and ending 5 years after publication.
- Access Criteria
- To gain access, requestors will need to provide a clear research aim or methodological sound research plan directed to the principal investigator (kkmshum@hku.hk).
The de-identified individual participant data collected during the trial will be available upon reasonable request.