Organization of the Cingulate Cortex (EEG-Feedback)
Structure-function Relationships Within the Cingulate Cortex
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Tilmelding (Faktiske)
Tilmelding
Fase
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Bron, Frankrig, 69677
- Hospices Civils de Lyon, Groupement Hospitalier Est
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- being able to provide a writen consent form
- having a social insurance
- have a normal vision (with or without corrections)
- Right-handed
Exclusion Criteria:
- Subjects with MRI contraindications (e.g. pacemaker, claustrophobia, metal in the body, etc…).
- Subjects must be willing to be advise in case of discovery of brain abnormality.
- No history of known neurological or psychiatric illness
- Pregnant or nursing women
- Persons under guardianship, curatorship or any other administrative or judicial measure of deprivation of rights or liberty, as well as legal persons protected by law
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Grundvidenskab
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
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Eksperimentel: 1
Each subject will conduct 3 sessions, i.e. a training session, an anatomical MRI session and an EEG session.
The first session will be to train the subject to carry out the different behavioral tasks that he will then have to perform during the session of EEG.
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Each subject will be trained to perform a trial-error learning task.
In this task, three visual stimuli will be presented to the subject.
The subject will have to find by trial-error, the one associated with positive feedback, the other stimuli being associated with negative feedback (search period).
Once the stimulus is associated with positive feedback, the subject will perform a period of repetition during which he will choose the stimulus associated with positive feedback.
Two variants of the task will be used: a variant in which feedback will be visual (ie positive feedback = green square, negative feedback = red square) and a variant in which feedback will be fruit juice (ie positive feedback = Fruit juice (but less than 2ml), negative feedback = no volume or small volume of fruit juice).
Once the tasks are learned, each subject will participate in an MRI session during which an anatomical scan will be obtained.
For each task, the time of presentation of the stimuli will be 2s.
During this time, the subject should indicate his choice of stimulus.
After a delay of 2s, feedback will be presented for 1s.
Each test shall be separated by an inter-test delay of 3s.
The presentation of the stimuli and the control of the answers will be managed by the E-prime or Presentation software.
Once the tasks are learned, each subject will participate in an MRI session during which an anatomical scan will be obtained and then an EEG session during which he will perform the task learned.For each task, the time of presentation of the stimuli will be 2s.
During this time, the subject should indicate his choice of stimulus.
After a delay of 2s, feedback will be presented for 1s.
Each test shall be separated by an inter-test delay of 3s.
The presentation of the stimuli and the control of the answers will be managed by the E-prime or Presentation software.
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Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Resting state fMRI data
Tidsramme: 3 years
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BOLD signal will be analyzed in the low frequency band (0.1-0.01Hz).
Images must be not too much distorted to allow data analysis.
As such, if a subject moved too much (translation>10mm; rotation>5°) the corresponding data will be excluded from the analysis.
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3 years
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EEG data
Tidsramme: 3 years
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If recordings are too noisy (if only <30% of trials survive the denoising process), subject will be excluded from final analysis.
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3 years
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Behavioral data in the EEG experiment
Tidsramme: 3 years
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Performance in the task will be assessed.
If performance in the task is <80%, subjects will be excluded in the final analysis.
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3 years
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Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Efterforskere
Efterforskere
- Ledende efterforsker: Christian SCHEIBER, MD, Hospices Civils de Lyon
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Studiestart
Primær færdiggørelse (Faktiske)
Primær færdiggørelse
Studieafslutning (Faktiske)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- 69HCL16_0659
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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