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Home-based Visual-motor Training Program on Kindergarteners

Effectiveness of Home-based Visual-motor Training Programs on At-risk Kindergarteners

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05605977
Enrollment
150
Registered
2022-11-04
Start date
2022-11-01
Completion date
2024-10-31
Last updated
2022-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Developmental Delay, Preterm Children

Keywords

visual motor, kindergarten children, developmental delay

Brief summary

The study aims to investigate the feasibility and effectiveness of the traditional and computerized home-based visual-motor training programs on at-risk kindergarteners.

Detailed description

The purpose of this project is to investigate the feasibility and effectiveness of home-based traditional visual-motor activities and tablet games on fine motor, visual perception, visuo-motor integration, handwriting performance, and adaptive behaviors of at-risk kindergarteners. At-risk kindergarteners will be randomized into the three groups: control, traditional, and tablet groups. In addition to regular early intervention, children in the traditional and tablet group will receive home-based visuo-motor training program with their parents. Children in the control group will only receive regular intervention during the study period.

Interventions

BEHAVIORALTraditional visual-motor training program

Traditional visual-motor program includes play and paper-and-pencil activities

BEHAVIORALComputerized visual-motor training program

Computerized visual-motor training program includes tablet visual-motor games

Sponsors

National Cheng-Kung University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

The assessors are blinded to the assigned group of participants

Intervention model description

pretest-posttest control group design

Eligibility

Sex/Gender
ALL
Age
5 Years to 6 Years
Healthy volunteers
Yes

Inclusion criteria

1. Either visual perception or fine motor score below the norm average 2. can follow instruction and complete the entire tests

Exclusion criteria

1. Visual or hearing problems that cannot be corrected to be normal 2. A diagnosis of significant neurological, muscular, and skeletal system disorders (e.g., Cerebral palsy) 3. A diagnosis of moderate or severe intellectual disabilities 4. Taking medication to control seizure or improve learning abilities

Design outcomes

Primary

MeasureTime frameDescription
the Test of Visual Perceptual Skills-Fourth Edition (TVPS-4)baseline, after 12 weeksthe change of visual-perceptual skills
the Bruininks-Oseretsky Test of Motor Proficiency-Second Edition (BOT-2)baseline, after 12 weeksthe change of fine motor skills
the Chinese Handwriting Testbaseline, after 12 weeksthe change of the Chinese handwriting performance

Secondary

MeasureTime frameDescription
the Game Questionnairethrough study completion, an average of one weekThe questionnaire is designed to measure the difficulty, participation, and liking level of playing the training games using 5-point Likert scale from parental view after the completion of the games.
The Berry-Buktenica Developmental Test of Visual-Motor Integration- Forth Edition (VMI)baseline, after 12 weeksthe change of VMI
Parental Feedback Questionnaireafter 12 weeksThe questionnaire consists of a few open-ended questions which are designed to realize parental experience of participating the home-based visual-motor training program.
the Vineland Adaptive Behavior Scales - Third Edition - Chinese Version (VABS-3-C) (Parents/Caregivers Edition)adaptive behaviorbaseline, after 12 weeksthe change of adaptive behavior
the test of Visual Perception of Chinese Charactersbaseline, after 12 weeksThe change of visual perception of Chinese characters

Contacts

Primary ContactYea-Shwu H Hwang, ScD
yshwang@mail.ncku.edu.tw886-62353535

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026