NCT06766149

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. 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. 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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
176

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Dec 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2024

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

January 3, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

January 9, 2025

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 23, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 23, 2025

Completed
Last Updated

April 29, 2026

Status Verified

April 1, 2026

Enrollment Period

1.1 years

First QC Date

January 3, 2025

Last Update Submit

April 27, 2026

Conditions

Keywords

executive functionchildrencomputerized cognitive trainingworking memorycognitive function

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

EXPERIMENTAL

The 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.

Behavioral: CogniFit Computerized Cognitive Training

Cogmed Group

ACTIVE COMPARATOR

The 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.

Behavioral: Cogmed Computerized Cognitive Training

Waitlist Control Group

NO INTERVENTION

The 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.

CogniFit Group

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.

Cogmed Group

Eligibility Criteria

Age6 Years - 12 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

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

Study Sites (1)

The University of Hong Kong

Hong Kong, Hong Kong

Location

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

The de-identified individual participant data collected during the trial will be available upon reasonable request.

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).

Locations