Inhibitory Control of the Mind : Neural Bases and Impact for Obsessive-compulsive Disorders (SUPTOC)
Etude en Imagerie Par résonance magnétique Fonctionnelle et Structurelle Des mécanismes de Suppression mnésique Dans Les Troubles Obsessionnels Compulsifs
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Calvados
-
Caen, Calvados, France, 14000
- GIP Cyceron
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria :
All the participants :
- Participants between 18 and 55 years old
- Affiliated to the French national health care system
- French native speaker
- Right-handed
- At least education after graduating with french GSCE "brevet des collèges"
- Body mass < 35kg/m2
Healthy subjects :
- Signed written consent form
Patients :
- Patients with OCD according to DSM V diagnostic criteria at the time of the study
- Stabilized (no change of psychotropic drugs during the last 3 months)
- Signed written consent form associated with the agreement of the tutor and / or curator for protected adults
Exclusion Criteria:
All the participants :
- Pregnancy or intent to get pregnant
- Person deprived of their liberty
- Person admitted to a health or social institution for purposes other than research
- Minor
- Protected adults or people unable to give informed consent
- Person subjected to an exclusion period related to another protocol
- History of cancer with the last 5 years, excluding squamous cell carcinomas
- Alcoholism, antecedents of chronic alcoholism or drugs abuse
- Use of medication that may interfere with cognitive or cerebral functioning
- Presence of visual or hearing troubles that may compromise participant's ability to participate in the study
- MRI Contraindications
Healthy subjects :
- History of neurological or psychiatric disorders or existence of traumatic brain injury with loss of consciousness for more than one hour
- Severe psychiatric disorders (according to DSM V diagnostic criteria) or psychological troubles which could affect participant's judgment
Patients :
- Presence of neurological history, history of head trauma with loss of consciousness for more than an hour, severe depression, manic symptoms, post-traumatic stress, borderline personality disorder, antisocial, paranoid or schizoid.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: patients with obsessive compulsive disorder
Functional magnetic resonance imaging behavioral measures physiological measurements
|
|
|
Experimental: healthy participants
Functional magnetic resonance imaging behavioral measures physiological measurements
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Blood Oxigen Level Dependent (BOLD) response as measured with fMRI
Time Frame: 1 hour
|
1 hour
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Investigators
Investigators
- Principal Investigator: Anaïs Vandevelde, MD, University Hospital, Caen
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Anticipated)
Primary Completion
Study Completion (Anticipated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- 2015-A01609-40
- 160028B-31 (Other Identifier: ANSM)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.