- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05035901
Geometric-Based Handwriting Intervention: Development, Feasibility and Randomized Clinical Trial
March 8, 2024 updated by: National Taiwan University Hospital
This study will focus on (1) developing the Chinese characteristic-based VMI-focused program, namely visual-perception motor-coordination integration program (CCVPMCI) involving the most Chinese-handwriting-related skills training and (2) investigating the effectiveness of the CCVPMCI program on handwriting performance in children with handwriting difficulties in Taiwan.
Study Overview
Status
Recruiting
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
72
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Tien Ni Wang, PhD
- Phone Number: +886 23366-8163
- Email: tnwang@ntu.edu.tw
Study Locations
-
-
-
Taipei, Taiwan, 100
- Recruiting
- National Taiwan University Department of Occupational Therapy
-
Contact:
- Tien Ni Wang, PhD
- Phone Number: 886 23366-8163
- Email: tnwang@ntu.edu.tw
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
7 years to 12 years (Child)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
1. poorer handwriting performance than the peers referred from teachers.
Exclusion Criteria:
- severe neurological or pervasive developmental disorders that might directly impeded writing
- intellectual disability that might directly impeded writing
- musculoskeletal, or sensory (hearing, vision) disorders that might directly impeded writing
- difficulty in reading or expressing
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: visual-perception motor-coordination integration program
Visual-perception motor-coordination integration program (CCVPMCI) is a Chinese characteristic-based VMI-focused program involving the most Chinese-handwriting-related skills training.
CCVPMCI mainly emphasizes the training role of visual-motor integration.
The idea of CCVPMCI program will involve (1) visual motor integration training affiliated with visual perception and motor coordination as warm-up exercise, (2) more focus on visual spatial perception in connect with unique visual structure of Chinese characters, (3) the trace or component elements of Chinese characters as the interesting practice material and (4) appropriate challenge for learning.
|
Visual-perception motor-coordination integration program (CCVPMCI) is a Chinese characteristic-based VMI-focused program involving the most Chinese-handwriting-related skills training.
CCVPMCI mainly emphasizes the training role of visual-motor integration.
The idea of CCVPMCI program will involve (1) visual motor integration training affiliated with visual perception and motor coordination as warm-up exercise, (2) more focus on visual spatial perception in connect with unique visual structure of Chinese characters, (3) the trace or component elements of Chinese characters as the interesting practice material and (4) appropriate challenge for learning.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The change from baseline Chinese Legibility Scale (CLS) at one month and six months
Time Frame: baseline, one month, six months
|
Chinese Legibility Scale is the self-develop assessment tool to investigate a child's handwriting legibility objectively.
Children will be asked to copied 10 Chinese characters on paper within 2*2cm squares to complete the copying paper.
Meanwhile, the performance time will be recorded when the child start writing the firs stoke until finish the last stroke of the last character.
These Chinese characters are selected from three versions of current mandarin textbooks according to each grade and those with high-frequency and around the average stroke counts will be chosen.
Then, characters can be classified into five types of structures based on the visual similarity of character, including top-down (vertical), left-right (horizontal), P-shaped, L-shaped and enclosed.
Ultimately, there are 20 characters in total for each grade with five types evenly.
The scale will be scored by a therapist blind to the experiment to decide children's writing legibility.
|
baseline, one month, six months
|
|
The change from baseline Chinese Handwriting Evaluation Form (CHEF) at one month and six months
Time Frame: baseline, one month, six months
|
The CHEF is an observational assessment designed to objectively measure the handwriting performance of school-aged children.
It is composed of 25 items and divided into five main dimensions, including construction, accuracy, direction of the characters, writing speed and pencil grip.
Items are descriptions of common writing problems by scored on 5-point Likert scale according to the frequency of the problem.
|
baseline, one month, six months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The change from baseline Developmental Test of Visual Perception - Third Edition (DTVP-3) at one month and six months
Time Frame: baseline, one month, six months
|
The DTVP-3 is commonly used as a standardized and norm-referenced test to assess visual perception skills for children aged 4 through 12 .
The testing time will range from approximately 20 to 40 minutes depending on the child's ability.
It is composed of 5 subscales: eye-hand coordination (EH), copying (CO), figure-ground (FG), visual closure (VC) and form constancy (FC).
The result of the five subtests can be combined to form three composites: motor-enhanced visual perception, motor-reduced visual perception, and general visual perception.
The first two subtests involve motor-enhanced visual perception skills and are summed together to represent visual-motor integration abilities.
The latter three subtests (FG, VC and FC) are non-motor involved and are summed together to represent motor-reduced visual perception.
The combination of motor-enhanced and motor-reduced visual perception could be the general visual perception skills.
|
baseline, one month, six months
|
|
The change from baseline Beery-Buktenica Developmental Test of Visual-Motor Integration at one month and six months
Time Frame: baseline, one month, six months
|
The Beery-Buktenica Developmental Test of Visual-Motor Integration is a standardized, norm-referenced test to assess visual-motor integration.
During the test, the child is required to copy a series of geometric designs, and his/her performance is compared with standard criteria and reference designs.
|
baseline, one month, six months
|
|
Pediatric Motivation Questionnaire (PMQ)
Time Frame: through study completion, an average of one month
|
The PMQ is an activity-based measurement of motivation and is designed to measure motivation and the experience of receiving specific therapeutic activities .
The items of PMQ are modified from existing questionnaires Pediatric Motivation Scale and based on tenets of self-determination theory.
The PMQ consists 12 items containing three motivation domain: (1) extrinsic motivation, (2) basic psychological needs, and (3) intrinsic motivation by 5-point Likert scale.
The PMQ represents the motivation condition through the intervention from children their own view.
In addition, several open-ended questions are added in children's version to reflect perspective of children while receiving the VPMCI program to obtain qualitative information.
|
through study completion, an average of one month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 27, 2021
Primary Completion (Estimated)
September 1, 2026
Study Completion (Estimated)
September 1, 2026
Study Registration Dates
First Submitted
August 23, 2021
First Submitted That Met QC Criteria
September 1, 2021
First Posted (Actual)
September 5, 2021
Study Record Updates
Last Update Posted (Actual)
March 12, 2024
Last Update Submitted That Met QC Criteria
March 8, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 202009039RIND
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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