Recruiting NCT06337500
Validation of a Making Decision Hybrid (Ecologic and Virtual) Task
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Neurophysiological measure (EEG), Survey.
- Who it may be relevant to
- Registry conditions: Healthy Volunteers, Behavior and Behavior Mechanisms. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
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.
Interventions
- Device Neurophysiological measure (EEG)
Cerebral electric activity recorded with EEG - Other Survey
Participants complete a survey to evaluate their exposure to screens and their assessment of the laboratory task performed
Primary outcome measures
- 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]
Eligibility criteria
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".
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Other
Study locations
France · 1 center
- CHU Besançon — Besançon
Identifiers
NCT: NCT06337500 · 2023/764