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The Effect of Virtual Reality on Motor Functioning and Participation Abilities Among Children With DCD

Not Applicable
Conditions
Developmental Coordination Disorder
Interventions
Device: Virtual Reality Timocco
Other: Conventional OT intervention
Registration Number
NCT02504385
Lead Sponsor
Clalit Health Services
Brief Summary

The subjet of this study is to explore the effect of using virtual reality environment at the clinic and at home (using Timocco) on the motor and participation abilities of children with DCD (Developmental Coordination Disorder).

The study will examine the efficacy of using virtual reality gaming environment (Timocco) for treating children with DCD and the use of remote therapy, by shifting the focus of therapy from the clinic to the home environment, using the remote control system of Timocco for home practice.

Detailed Description

The efficacy of using VR (Virtual Reality) as a therapeutic tool as an integral part of Occupational Therapy intervention will be examined in this study. The study will be conducted in two stages: the first will be conducted at the Child Development Center of the Clalit HMO (Health Maintenance Organization), and the second will take place in the child's home.

The first intervention will take approximately 8 to 10 weeks, during which eight data collection sessions will be conducted, each of 45 minutes duration.

The study group will integrate the use of Timocco in occupational therapy sessions while the control group will be given conventional occupational therapy without using Timocco.

In the second intervention, the study group will be given access to the virtual-reality environment of Timocco to be used at home, and will not include therapy sessions at the Child Development Center. An assessment before and after intervention will be held for both groups for comparison.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Male
Target Recruitment
30
Inclusion Criteria
  • Children,
  • native Hebrew speakers, between the ages of 4 and 6 diagnosed with DCD.
Exclusion Criteria
  • Children with complicated special needs (e.g., limited cognitive abilities, CP, ASD),
  • children who received occupational or physical therapy interventions in the last 12 months.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Virtual Reality TimoccoVirtual Reality TimoccoThe study group will integrate the use of Timocco in occupational therapy sessions. The session will begin with 15 minutes of spatial activity involving sensory-motor practice, 15 minutes of activity in a virtual environment, and 15 minutes of structured activity at a desk.
Conventional OT interventionConventional OT interventionThe control group will be given conventional occupational therapy without using Timocco. In order to ensure that the therapy sessions in this group have a structure similar to that one used in the study group, each session will include 25 to 30 minutes of spatial sensory-motor activity, followed by 15 to 20 minutes of structured practice at a desk.
Primary Outcome Measures
NameTimeMethod
The score in Motor and participation assessments (Henderson, S. & Sugden, D. 1992)up to 18 weeks
Score in Timocco virtual reality system (number of wrong moves; Correct moves;response time)up to 18 weeks

data will be gathered using Timocco for the entire intervention

Secondary Outcome Measures
NameTimeMethod
DTVP-2 (developmental test of visual perception, 1993))Baseline

Screening test.

DCD-Q (BN. Wilson, BJ. Kaplan, SG. Crawford and G. Roberts, 2009)up to 18 weeks

The questionnaire will be filled once at the beginning, once again at the end of phase 1 (in the clinic) , and last time after home practice (the second phase).

Participation questionnaire (Yarus, 2010)up to 18 weeks

The questionnaire will be filled once at the beginning, once again at the end of phase 1 (in the clinic) , and last time after home practice (the second phase).

Satisfaction questionnaireup to 18 weeks
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