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NCT00364702 Clinical Trial

Virtual Reality a Novel Screening and Treatment Aid in Attention Deficit Disorder

ADHD Clinical Trial

Official title:
Virtual Reality a Novel Screening and Treatment Aid in Attention Deficit Disorder

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00364702
Other study ID # 45/04
Secondary ID
Status Completed
Phase Phase 2
First received August 15, 2006
Last updated August 16, 2011
Start date August 2006
Est. completion date July 2007

Study information
Verified date July 2006
Source Shaare Zedek Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

Using a virtual reality program in screening and treatment of ADHD.

Description:

Virtual Reality is a novel program designed to imitate a real classroom environment including various distractions. It includes a head monitor to track eye movements Children aged 10-20 years with ADHD will use the program with and without methylphenidate(1 mg/kg). Their results will be compared to a control group.

Parental consent will be obtained.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date July 2007
Est. primary completion date July 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 10 Years to 20 Years
Eligibility Inclusion Criteria:

Clinical diagnosis of ADHD-DSM4 criteria AGE 10-20 YEARS normal neurological examination IQ>80

Exclusion Criteria:

ABNORMAL NEUROLOGICAL STATUS

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

  • ADHD
  • Attention Deficit Disorder with Hyperactivity

Intervention

Drug:
• methylphenidate

Locations
Country Name City State
Israel Shaari Zedek Pediatric Neurology Unit Jerusalem

Sponsors (1)
Lead Sponsor Collaborator
Shaare Zedek Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Virtual Reality program test results
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