Skip to main content
OpenTrials
Active, Not Recruiting

NCT Number: NCT07057024

Contribution of Virtual Reality Eye Tracking in the Identification of Schizophrenia, Bipolar and Depression

Schizophrenia (SCZ), bipolar disorder (BP), and depression (DEP) are systematically associated with a severe impairment of the overall abilities of patients, which precludes them from functioning adequately in daily life. A large body of literature emphasises the importance of identifying specific markers for these pathologies to prevent or anticipate the emergence of new psychopathological symptoms.

As a result, one of the current research challenges is to develop new, faster, and more reliable tools. Eye movements are physiological signs involving brain areas that control cognitive processes. These same processes could be altered in psychiatric disorders, and these alterations could produce many eye movement abnormalities.

The literature highlights some eye movement abnormalities specific to each targeted pathology. However, to our knowledge, no study has compared eye movement abnormalities in a virtual environment projected in a head-mounted display (HMD).

The investigators hypothesised that an eye tracker connected to an HMD could identify specific eye movement abnormalities of SCZ, BP, and DEP. Recording eye movements specific to these pathologies in pseudo-ecological situations could lead to better identification methods.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Notify Me

Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Etablissement Public de Santé Barthélemy Durand

Étampes, 91 150, France

About this study

Schizophrenia (SCZ), bipolar disorder (BP), and depression (DEP) are among the most incapacitating pathologies. Specific abnormalities such as characteristics of fixations (stability of the eye) and saccades (movement between one fixation point to an another) are proposed as endophenotypic markers of these diseases, particularly in SCZ and BP.

In SCZ, literature reports as core abnormalities a saccadic pursuit in the Smooth Pursuit Eye Movement (SPEM) and a restricted field of exploration in free-viewing. In BP, fixation times and eye movement velocity during free-viewing differ from those identified in SCZ. When psychotic features are present, BP's pursuit movement is similar to SCZ's. Moreover, eye movement abnormalities are correlated with the presence of manic/hypomanic or depressive symptoms, even in or saccadic paradigms (i.e., anti-saccade or guided memorisation). In DEP, eye movements are significantly different from BP regarding movement velocity, while fixation times are similar in the saccade or free viewing paradigms. In addition, pursuit movements are not saccadic in the SPEM task.

Nevertheless, studies do not necessarily use equipment with the same performance, and eye-tracking technology constantly evolves. Eye-tracking can now be included in Virtual Reality (VR) Head- Mounted Displays, permitting the creation of new pseudo-ecological paradigms.

The investigators hypothesise that abnormalities in eye movements in SCZ, BP, and DEP will be identifiable in VR environments compared to healthy controls, and could differentiate them one from the other.

Participants will be assessed using scales and questionnaires and eye-tracking in VR environments. The data will be analysed using statistical processing to identify significant differences in eye movements between SCZ, BP, and DEP and healthy controls.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

For all participants:

  • Male or female, aged 18 to 60 years
  • Subject having given their written consent to the study For Schizophrenia participants :
  • Diagnosis of schizophrenia according to DSM-V criteria and stabilised for at least three months

For bipolar disorder participants :

  • Diagnosis of bipolar disorders according to DSM-V criteria and stabilised for at least three months

For depressive disorders participants :

  • Diagnosis of depressive disorders according to DSM-V criteria and stabilised for at least three months

Exclusion criteria

For all the participants :

  • Subjects unable to give consent or not volunteering for the study.
  • Current(s) somatic(s) condition(s)
  • Specific ophthalmological problems (strabismus, amblyopia) incompatible with the devices stereoscopic (VR headsets)
  • Head trauma's history with loss of consciousness
  • Epilepsy history
  • Intellectual disability
  • Difficulties in understanding the French language
  • Current or during the last 6 months of substance abuse or dependence (except tobacco)
  • Freedom restriction by judicial or administrative decision and/or coercive hospitalisation
  • Cybersickness history
  • Pregnancy

For healthy control group :

  • Current or previous psychiatric disorder
  • Current psychotropic drug therapy

Treatment and study plan

Clinical and eye movements

Other

Eye tracking in virtual reality environment:

Clinical and psychometric assessment :

  • Auto-assessment scales : Fagerström Test For Nicotine Dependance (FTND), Annett handedness questionnaire, Alcohol Use Disorders Identification Test (AUDIT), Substance Use Risk Profile Scale (SURPS), Generalized Anxiety Disorder-7 (GAD-7)
  • Hetero-assessment scales : Young Mania Rating Scale (YMRS), Hamilton Depression Scale (HDRS), Positive And Negative Scale for Schizophrenia (PANSS)

Primary outcomes

  1. Record dwell time (millisecond) and saccadic parameters (millisecond and degree) using an eye-tracker connected to a virtual reality HMD. Then, compare each measure to identify schizophrenia, bipolar, depression and control group differences.

    Time frame: 90 minutes

    Comparison of eye-tracking metrics in schizophrenia, bipolar disorder, depression, and control groups using virtual reality.

Secondary outcomes

  1. Correlations between clinical and psychometric assessment results and eye-tracking metrics recorded in virtual reality

    Time frame: 95 minutes

    Clinical and psychometric assessment.

    • Eye-tracking metrics: Record dwell time (millisecond) and saccadic parameters (millisecond and degree) using an eye-tracker connected to a virtual reality headset during the presentation of the environment. Recorded for the primary outcome.
    • Hetero-assessment:
    • Positive And Negative Scale for Schizophrenia (PANSS) This scale is aimed to assess the positive and negative symptoms for schizophrenia.(45 minutes)
    • Young Mania Rating Scale (YMRS) This scale is aimed to assess manic and hypomanic symptoms.(15 minutes)
    • Hamilton Depression Scale (HDRS) This scale is aimed to assess depressive symptoms.(15 minutes)
    • Auto-assessment:
    • Generalized Anxiety Disorder-7 (GAD-7). This scale evaluates the symptoms of anxiety. (10 minutes)
    • Substance Use Risk Profile Scale (SURPS).This scale assesses several personality risk factors for addiction and psychopathology. (10 minutes)

Sponsors and collaborators

Lead sponsor

Etablissement Public de Santé Barthélemy Durand

Other

Collaborators

  • Aix Marseille Université
  • Hopital Paul Brousse
  • Institut National de la Santé Et de la Recherche Médicale, France

Registry information

Acronym: ReViPSY

Important dates

Study start
2026
Primary completion
2028
Study completion
2029
First posted
Jul 9, 2025
Registry last updated
Mar 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.