- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06246318
Effects of VR in Children With DCD: Randomized Controlled Trial
Effects of Virtual Reality in Children With Developmental Coordination Disorder: Randomized Controlled Trial
The aim of the study is to examine the effect of VR application on motor, cognitive and sensory-perceptual skills, and activity and participation levels in children with DCD.
The hypotheses on which the study proposal is based are as follows:
- H0: VR application has no effect on motor skills in children with DCD. H1: VR application has an effect on motor skills in children with DCD.
- H0: VR application has no effect on cognitive skills in children with DCD. H1: VR application has an effect on cognitive skills in children with DCD.
H0: VR application has no effect on sensory-perception skills in children with DCD.
H1: VR application has an effect on sensory-perception skills in children with DCD.
H0: VR application has no effect on the functional independence levels in daily living activities in children with DCD.
H1: VR application has an effect on the functional independence levels in daily living activities in children with DCD.
- H0: VR application has no effect on participation levels in children with DCD. H1: VR application has an effect on participation levels in children with DCD.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Within the scope of our aims;
- To determine the gross motor skill levels of children with DCD and to obtain the effect of VR application on gross motor skill levels.
- To determine the executive function skill levels of children with DCD and to obtain the effect of VR application on executive function skill levels.
- To determine the sensory-perception skill levels of children with DCD and to obtain the effect of VR application on sensory-perception skill levels.
- To determine the functional independence of children with DCD in daily life and to obtain the effect of VR application on their functional independence levels.
- It is aimed to determine the participation levels of children with DCD and to obtain the effect of VR application on their participation levels.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Sıhhiye
-
Ankara, Sıhhiye, Turkey, 06100
- Hacettepe University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being between 5-8 years old,
- It is to get 15-46 points from the Developmental Coordination Disorder Questionnaire for ages 5-7 and 15-55 points for ages 8.
Exclusion Criteria:
- Those who are receiving any other therapy program,
- have vision (other than glasses) or hearing problems,
- Children with any neurological disorder will not be included in the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: virtual reality plus conventional occupational therapy
Virtual reality will be given to the study group in addition to the conventional occupational therapy program. Nintendo Wii Fit Plus will be used as the virtual reality method in the research. |
The virtual reality protocol here is based on perceptual-motor activities, supported by Nintendo Wii resources.
The user will be able to control a game character in a virtual environment using a remote control with a motion sensor.
Wii Fit Plus requires the use of the Wii Balance Board that the player stands on during gameplay.
The Wii Balance Board is not a wobbly balance board, but is able to detect and track the user's center of balance, a feature used extensively in the game.
Wii Fit Plus includes more than 40 activities including yoga, strength training, aerobics and balance games.
During the virtual reality application, different games will be preferred in each session depending on the duration of the games.
Virtual reality application will be carried out in a corner prepared for virtual reality application in the room where the conventional occupational therapy session is held.
Families have the right to observe and attend all sessions whenever they wish.
Sensory integration and gross motor training approaches will be used in the conventional occupational therapy program. A manualized protocol based on Ayres sensory integration principles will be followed (Schaaf et al., 2012). The intervention will be carried out by a licensed occupational therapist trained in sensory integration. This approach suggests that if a child engages in individually adapted sensorimotor activities, the nervous system is better able to modulate, organize, and integrate sensory information and is also more likely to use sensory information in adaptive ways (Ayres, 1972). Components of the intervention include a sensory-rich, playful, child-centered approach, providing a decision challenge, and facilitating increasingly complex adaptive behaviors by engaging the child in individually tailored, developmentally appropriate play interactions |
Other: conventional occupational therapy
This is a control group.
Sensory integration and gross motor training approaches are used in the conventional occupational therapy program.
|
Sensory integration and gross motor training approaches will be used in the conventional occupational therapy program. A manualized protocol based on Ayres sensory integration principles will be followed (Schaaf et al., 2012). The intervention will be carried out by a licensed occupational therapist trained in sensory integration. This approach suggests that if a child engages in individually adapted sensorimotor activities, the nervous system is better able to modulate, organize, and integrate sensory information and is also more likely to use sensory information in adaptive ways (Ayres, 1972). Components of the intervention include a sensory-rich, playful, child-centered approach, providing a decision challenge, and facilitating increasingly complex adaptive behaviors by engaging the child in individually tailored, developmentally appropriate play interactions |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Test of Gross Motor Development-2
Time Frame: It will be applied 8 weeks after the first evaluations are made.
|
Assessment of gross and fine motor skills
|
It will be applied 8 weeks after the first evaluations are made.
|
Sensory İntegration and praxis test
Time Frame: It will be applied 8 weeks after the first evaluations are made.
|
It is a standardized test developed by Ayres that evaluates in detail sensory perception and sensory perception-related skills in children between the ages of 4 and 8 years and 11 months.
SIPT consists of a total of 17 subtests.
|
It will be applied 8 weeks after the first evaluations are made.
|
Motor-Free Visual Perception Test-3
Time Frame: It will be applied 8 weeks after the first evaluations are made.
|
Assessment of visual perception
|
It will be applied 8 weeks after the first evaluations are made.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Participation and Environment Measure for Children and Youth (PEM-CY)
Time Frame: It will be applied 8 weeks after the first evaluations are made.
|
The PEM-CY is a measure that evaluates participation in the home, at school, and in the community, alongside environmental factors within each of these settings.
|
It will be applied 8 weeks after the first evaluations are made.
|
CHILDHOOD EXECUTIVE FUNCTIONING INVENTORY (CHEXI) FOR PARENTS AND TEACHERS
Time Frame: It will be applied 8 weeks after the first evaluations are made.
|
Working memory and inhibitory control levels will be evaluated with CHEXI.
|
It will be applied 8 weeks after the first evaluations are made.
|
Functional Independence Measure for Children (WeeFIM)
Time Frame: It will be applied 8 weeks after the first evaluations are made.
|
functional independence was assessed with the Functional Independence Measure for Children (WeeFIM).
|
It will be applied 8 weeks after the first evaluations are made.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: zeynep kolit, MSc, Hacettepe University
- Study Director: Sedef şahin, PhD, Hacettepe University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- VR24
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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