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Clinical Trial Summary

The objective of this research is to develop original virtual reality scenarios and/or new virtual reality equipments to evaluate or diagnose pathologies, such as attention deficit disorders or neuropsychiatric pathologies, addiction, anxiety or depression or pathologies interfering with sleep/wake disorders.


Clinical Trial Description

Nature of the trial: without direct individual benefit study conducted in healthy volunteers, patients with attention disorders : ADHD (Attention Deficit Disorder / Hyperactivity) and cognitive aging, addictive disorders, anxiety disorders, depressive disorders or pathologies that interfere with sleep/wake cycle. The duration of the study is 8 years.

Type of trial: Comparison of two parallel groups of healthy volunteers and patients with attention disorders, addictive, anxious, depressive or interfering with sleep/wake cycle.

Study design:

- standardized clinical interview with a sleep specialist, psychiatrist, or psychologist and rating scales,

- a virtual reality task. The primary outcome is to evaluate the diagnosis accuracy and the acceptability of the virtual tool to the referent standard (clinical interview and scales).

The secondary outcomes are:

- The comparison of healthy subjects and patients performances

- Tolerance, acceptability to exposure to virtual scenarios. ;


Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Screening


Related Conditions & MeSH terms


NCT number NCT02544295
Study type Interventional
Source University of Bordeaux
Contact Pierre PHILIP, MD-PhD
Phone +33557820172
Email pr.philip@free.fr
Status Recruiting
Phase N/A
Start date January 2012
Completion date January 2019

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