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

C

Clalit Health Services

Status

Unknown

Conditions

Developmental Coordination Disorder

Treatments

Device: Virtual Reality Timocco
Other: Conventional OT intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT02504385
COM 0024-14

Details and patient eligibility

About

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.

Full 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.

Enrollment

30 estimated patients

Sex

Male

Ages

4 to 6 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Virtual Reality Timocco
Experimental group
Description:
The 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.
Treatment:
Device: Virtual Reality Timocco
Conventional OT intervention
Active Comparator group
Description:
The 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.
Treatment:
Other: Conventional OT intervention

Trial contacts and locations

0

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Central trial contact

Ruth Terkel-Dawer, M.D; Sarit Tresser, M.Sc

Data sourced from clinicaltrials.gov

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