Conflict Detection Development During the Reasoning

NCT ID: NCT02788968

Last Updated: 2016-06-02

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 44 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-09-30
• Study Completion Date: 2017-10-31

Brief Summary

The study to explore the development of these abilities with age, and called "Development of the conflict detection during the reasoning - Decor" will take place at CYCERON center and will include two groups of 22 participants: adolescents and young adults (N = 44). More specifically, this study aims to compare the changes in the brain of adolescents and young adults when conducting reasoning tasks for which there may be a cognitive conflict. Both groups of participants then spend an MRI (Magnetic Resonance Imaging) focused on the brain and in which they will carry out two classic tasks covering the main areas of reasoning (probabilistic and economic). Each of these tasks will be manipulated to include, or not, of making information call intuition to create or not a conflict between the correct answer (logic, normative) and biased response (intuitive, heuristic). Because of the major implication of this brain region in cognitive inhibition processes [of intuitive answer], measured brain activity in the anterior cingulate cortex (ACC) during both tasks version "with" or "no" conflict will be compared between groups. To better understand the links between the development of the CCA from adolescence to adulthood and conflict detection, activity measurements will be correlated with a part in morphometric measurements taken from the same area (volume Substance Grise - SG; characteristics of cortical sulci) and secondly to cognitive measures (executive functions - inhibitory control). This cross-sectional study focused on two age groups: 11-15 years and 19-25 years. For each age group, the participation of men / boys and women / girls will be balanced up.

Conditions

Healthy Volunteers

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Blinding Strategy: NONE

Study Groups

Adolescents

MRI 11-15 years

Group Type: OTHER

MRI

Intervention Type: OTHER

Conventional reasoning tasks in both " with" and "without" cognitive conflict and realized during an MRI

Young adults

MRI 19-25 years

Group Type: EXPERIMENTAL

MRI

Intervention Type: OTHER

Conventional reasoning tasks in both " with" and "without" cognitive conflict and realized during an MRI

Interventions

MRI

Conventional reasoning tasks in both " with" and "without" cognitive conflict and realized during an MRI

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Healthy and educated adolescents aged 11-15 years
• boy or girl
• French mother tongue
• Handedness : right
• Having been informed by the teen booklet and given its written consent, and whose parents or legal guardian will be ( a) signed the informed consent sheet of the protocol
• Medical examinations , neurological, neuroradiological norma

or

• All healthy young adults aged 19-25 years at university level or in the workforce
• man or woman
• Level ≥ 12 years of study (bachelor level )
• Native language: French
• Handedness : right
• Signing of the informed consent of the protocol
• Medical examinations , neurological, neuroradiological norma

Exclusion Criteria

• Does not meet the targeted age groups
• Presents against -indications to MRI (severe claustrophobia , foreign bodies cons -indicated )
• This chronic intake of alcohol or drugs
• Cognitive disorders who could testify sudden onset of a stroke ; a history of head injury with loss of consciousness for more than 1 hour , or encephalitis
• A neurological chronic condition , psychiatric, endocrine , hepatic and infectious
• Major disease history (diabetes, chronic lung disease, heart disorder, metabolic , hematologic , endocrine or immunological severe, cancer)
• A medication that may interfere with brain imaging measures ( psychotropics, hypnotics, anxiolytics , neuroleptics, anti -Parkinson , benzodiazepines, anti-inflammatory drugs , antiepileptics, antihistamines , analgesics and muscle relaxants central ) .
• Manual predominantly left (after the first phone call with the contact person of CYCERON ; see section 9.1)
• Color Blindness
• Inability to submit the study for geographical or psychiatric reasons
• Pregnant and lactating women

The following criteria are specific to the adolescent group :

• Has pervasive developmental disorders and / or acquisitions identified by parents or legal guardian and (or ) the teachers
• Parents or legal guardian are not affiliated to a system of social security
• Unaccompanied by parent (s) (s) or legal guardian during the visit to CYCERON center

The following criteria are specific to the group of young adults :

• Non- affiliated to a social security scheme
• Be protected adult

• Minimum Eligible Age: 11 Years
• Maximum Eligible Age: 25 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Cyceron

UNKNOWN

Sponsor Role: collaborator

University Hospital, Caen

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Wym WN De Nyes, PhD

Role: STUDY_DIRECTOR

Cyceron

Locations

CHU Caen

Caen, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Olivier EO Etard, MCU-PH

Role: CONTACT

etard-o@chu-caen.fr

02.31.06.45.26 ext. + 33

Other Identifiers

2014-A00935-42

Identifier Type: -

Identifier Source: org_study_id