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NCT Number: NCT06337500

Validation of a Making Decision Hybrid (Ecologic and Virtual) Task

The aim of this study is to validate a new hybrid (ecological + virtual) decision-making tool. The difference in behavior (risky choices) between the "hybrid" task and the "virtual" task will be evaluated.

Recruiting

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Key information

Conditions

Healthy Volunteers Behavior Behavior and Behavior Mechanisms

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU Besançon

Besançon, Not in US/Canada, France

Location status: Recruiting

Location contact

Karine Charrière

CONTACT

[email protected]

+33381218999

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Men and women aged 18 to 65 inclusive
  • Subjects with no neurological or psychiatric disorders
  • Subjects with no addictive disorder except tobacco
  • Signed informed consent indicating that the subject has understood the purpose and procedures of the study and agrees to participate in the study and to abide by the requirements and restrictions inherent in the study
  • Affiliation with a French social security scheme or beneficiary of such a scheme.

Exclusion criteria

  • Men and women under 18 or over 65 years of age
  • Subjects suffering from a neurological or psychiatric disorder
  • Subjects suffering from an addictive disorder, with the exception of tobacco
  • Legal incapacity or limited legal capacity
  • Subject unlikely to cooperate with the study and/or poor cooperation anticipated by the investigator
  • Subject without health insurance
  • Pregnant
  • Subject within the exclusion period of another study or on the "national volunteer list".

Treatment and study plan

Neurophysiological measure (EEG)

Device

Cerebral electric activity recorded with EEG

Survey

Other

Participants complete a survey to evaluate their exposure to screens and their assessment of the laboratory task performed

Primary outcomes

  1. Validation of the homemade "Lab-Life" interface as a tool for simulating an ecological task with sufficient fidelity, while meeting the conditions required for recording high-quality brain activity using an EEG-HR.

    Time frame: Day 1

    Behavioral score obtained after completion of the hybrid task (netscore obtained at the IGT). This score can be compared with the scores obtained after the ecological and virtual tasks.

Study contacts

Contact information is provided by the study sponsor or research team.

Karine CHARRIERE, PhD

CONTACT

[email protected]

+333 81218999

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Besancon

Other

Registry information

Acronym: LABLife

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Mar 29, 2024
Registry last updated
Jul 18, 2025

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.

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