Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:37 AM
Ignite Modification Date:
2025-12-25 @ 4:37 AM
NCT ID:
NCT03967418
Eligibility Criteria:
Inclusion Criteria for all participants:
* More than 15 years and 3 months old
* Mastering the French language
* Social Security Affiliates
* Having given consent
* Correct level of vision allowing the reading of instructions, the distinction of shapes and colours and the understanding of shapes and images presented in cognitive tasks (subjectively attested by the patient)
* Correct hearing level, allowing a good understanding of the sounds presented (subjectively attested by the patient and the assessor at the first contact for eligibility)
Inclusion criteria for patients:
* Suffering from one of the behavioural addiction explored
* Beginning treatment in the Addictology department of the University Hospital of Nantes
Inclusion criteria for healthy volunteers:
\- Free from the explored behavioural addictions
Exclusion Criteria for all participants:
* Current and not stabilized psychiatric and addictive disorders (mood disorders, anxiety disorders and substance-use disorders except nicotine, lifetime psychotic syndrome), diagnosed by the MINI and after consultation with the clinician,
* Non stabilized endocrine disorders
* Neurological disorders (such as head trauma, neurodegenerative diseases, unbalanced epilepsy, mental retardation, etc.),
* Taking a psychotropic treatment wich is not stabilized for at least 2 weeks,
* Consumption of a psychoactive substance - other than nicotine - within the 12 hours prior to the assessment,
* Color blindness
* Cardiac problems self-reported by the patient, in order to avoid bias in the measurement of cardiac parameters,
* Electrical implants as declared by the participant (to avoid measurement artifacts)
* Having benefited from current or past cognitive remediation program
* Reporting being pregnant or breastfeeding
* Current participation or in the past month in a pharmacological research protocol
* Presenting difficulties for reading or writing French
* Being under guardianship
* With significant cognitive impairment not compatible with de cognitive assessment
Exclusion criteria for healthy volunteers :
\- Suffering from one of the behavioural addiction explored
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
15 Years
Study:
NCT03967418
Study Brief:
Protocol Section:
NCT03967418