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.
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 Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
SCREENING
Masking
NONE
Enrollment
590
University Hospital of Bordeaux
Bordeaux, France
RECRUITINGPresence or absence of the disease
Categorial diagnosis generated by the psychiatrist and by the Virtual reality task (0=absence of disease and 1 = presence of the disease)
Time frame: 1 day
Sleepiness scale
Scores range from 0 (no sleepiness) to 24 (severe sleepiness)
Time frame: 1 day
BDI-II questionnaire
Beck Depression Inventory Scores range from 0 (no depression) to 63 (severe depression)
Time frame: 1 day
IDS-R questionnaire
Inventory of Depressive Symptomatology scores range from 0 (no depression) to 84 (severe depression)
Time frame: 1 day
Acceptability scale
Scores range from 0 to 36
Time frame: 1 day
ASRS
Adult ADHD Self-Report Scale Scores : Four or more positive answers in Part A (6 questions) are indicative of ADHD symptoms.
Time frame: 1 day
Physiological parameters: Polysomnography (total sleep time (min))
Time frame: 1 night
Physiological parameters: Polysomnography (sleep structure (stage %))
Time frame: 1 night
Physiological parameters: Polysomnography (Apnea/Hypopnea index and Periodic movements index (events/hr))
Time frame: 1 night
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.