Interactive Digital Game for Improving Visual Perceptual Defects in Children With Developmental Disability

Sponsor
Kaohsiung Medical University Chung-Ho Memorial Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT05016492
Collaborator
(none)
23
1
2
12
1.9

Study Details

Study Description

Brief Summary

Visual perceptual defects in children can negatively affect their activities of daily living.The aims of this study were to develop and evaluate an interactive digital game system for correcting visual perceptual defects and to evaluate the effectiveness of the proposed system.

Condition or Disease Intervention/Treatment Phase
  • Device: Visual-perceptual interactive game system
  • Behavioral: standard rehabilitation
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
23 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Interactive Digital Game for Improving Visual Perceptual Defects in Children With Developmental Disability: Evaluation of Efficacy and User Satisfaction
Actual Study Start Date :
May 24, 2016
Actual Primary Completion Date :
May 23, 2017
Actual Study Completion Date :
May 23, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Digital game group

The digital game group received the standard 4-week course of rehabilitation but with an additional 30-min interactive digital game training session per week.

Device: Visual-perceptual interactive game system
Subjects received 30-min interactive digital game training session per week. The game system contain 7 skills training, each of which was named according to the corresponding TVPS-3.

Behavioral: standard rehabilitation
Subjects received the standard 4-week course of rehabilitation delivered in one 30-min session per week. The course of rehabilitation included: sensory integration therapy, cognitive function training and visual perception/auditory attention training.

Active Comparator: Standard rehab group

The standard rehab group received the standard 4-week course of rehabilitation delivered in one 30-min session per week.

Behavioral: standard rehabilitation
Subjects received the standard 4-week course of rehabilitation delivered in one 30-min session per week. The course of rehabilitation included: sensory integration therapy, cognitive function training and visual perception/auditory attention training.

Outcome Measures

Primary Outcome Measures

  1. Test of Visual Perceptual Scale-3(TVPS-3) [4 weeks]

    TVPS-3 is a standardized and norm-referenced task for children age 4-13 years that uses a response format suitable for all children, including those with disabilities. It includes subtasks of visual discrimination, visual memory, visual-spatial relationships, form constancy, visual sequential memory, figure ground, and visual closure (Martin et al., 2006). Each of the seven subtests has 16 items of varying difficulty. Therefore, the test has 112 total questions.

  2. User satisfaction survey [4 weeks]

    The 20-item questionnaire content was divided into five themes: perceived ease of use (6 questions), perceived usefulness (4 questions), perceived joyfulness (4 questions), satisfaction (3 questions), and continued use (3 questions). Questionnaire items were answered on a Likert scale from 1 (completely disagree) to 5 (completely agree).

  3. Test of the visual-perceptual interactive game system [4 weeks]

    The digital game test had 7 subtests, and each subtest had 10 questions. Based on the seven-item rules of TVPS-3, 1 point was assigned to each question, for a score of 10 points for each subtest, and a total score of 70.

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Years to 10 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Record of developmental disability diagnosis

  • Ability to understand instructions

  • TVPS-3 score lower than 25% of the norm reference and diagnosis of visual perceptual defect

  • Test of Nonverbal Intelligence-3rd Edition score higher than 70

Exclusion Criteria:
  • Did not follow or understand the instructions for participating in the study

  • Had severe defects in vision, hearing, etc.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kaohsiung Medical University Kaohsiung Taiwan 80708

Sponsors and Collaborators

  • Kaohsiung Medical University Chung-Ho Memorial Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kaohsiung Medical University Chung-Ho Memorial Hospital
ClinicalTrials.gov Identifier:
NCT05016492
Other Study ID Numbers:
  • KMUHIRB-SV(II)-20150090
First Posted:
Aug 23, 2021
Last Update Posted:
Aug 23, 2021
Last Verified:
Aug 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
Yes
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 23, 2021