NCT02850393

Brief Summary

Mental-health conditions affect million people worldwide. The economic burden of mental illness is enormous and the economic health of both developing and developed nations will depend on controlling the staggering growth in costs from mental disorders. Obsessive-compulsive disorder (OCD) is a relatively common and frequent form of anxiety that affects approximately 2-3% of the population. OCD is characterized by anxiety, obsessions (persistent intrusive thoughts and images with highly distressing contents) and compulsions (repetitive activity), and severely impairs the lives of those affected. Despite their interest as effective and affordable care and rehabilitation, cognitive therapeutic profits too little from the increasing accumulation of knowledge in neuroscience, and neuroscientists pay too little attention to the challenges faced by clinical psychologists and psychiatrists. To reduce this cultural gap, two teams specialized in the study and multimodal imaging of healthy participants and clinical patients with mental health disorders, the UMR-S INSERM-EPHE-UNICAEN U1077 unit led by Francis Eustache, and ISTS team (UMR-S 6301 CNRS-CEA-UCBN) led by Sonia Dollfus, will joint their efforts to develop an integrated approach of the neural mechanisms at stake from basic neuroscience using state-of-art neuroimaging techniques, to novel and ground breaking psychological intervention. Both teams evolve at the brain imaging Cyceron center in Caen in connection with the Mental Health and Addictology Center, offering unique opportunities for such translational research. This project will capitalize on recent evidence showing that healthy participants can prevent unwanted images from entering consciousness using inhibitory control and memory suppression techniques, disrupting traces of the memories in sensory areas of the brain, and weakening their vividness and later reentrance. OCD is characterized by aberrant and excessive visual intrusions, usually extremely vivid, detailed, and unpleasant. These distressing images are particularly uncontrollable and may frequently initiate compulsive rituals. In a first phase of this proposal will use functional magnetic resonance imaging (fMRI) to develop a neurobiological model of the cognitive computations achieved by inhibition network to suppress memory. To achieve this goal we will develop an attentional model of healthy memory inhibition functioning, simulating the deployment of attentional resources and the different mental processes at stake during suppression. Using sophisticated analyzing tools of fMRI data, we will use this model to decode and infer the representational content of the brain inhibition network, and further refine the connectivity pathways which underlie such control. The lack of a strong neurobiological model prevents the development of therapies which would increase functionality of this network and optimize intervention aiming to disrupt mental intrusions and obsessions. In a second phase, we will assess whether memory suppression may be transferred and trained in OCD patients using images depicting their own obsessions, as a promising avenue to reduce their symptoms on the long run. In addition, fMRI and other brain structural acquisitions will be collected before and after cognitive training to memory suppression, offering a unique opportunity to observe the online dysfunction of intrusion control in OCD patients and to identify neurobiological markers predictive of training outcome and network reconfiguration with training. A fundamental goal of motivated forgetting involves not only to exclude unwelcome content from consciousness but also to reduce their later emotional impact by doing so. In parallel of these two main phases, we will thus also measure physiological markers of autonomic nervous system activity changes in response to suppressed images to better identify the consequences of memory suppression on emotional states, anxiety, and mental health in general.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
48

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2016

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 27, 2016

Completed
1 month until next milestone

Study Start

First participant enrolled

July 1, 2016

Completed
1 month until next milestone

First Posted

Study publicly available on registry

August 1, 2016

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2019

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2019

Completed
Last Updated

August 1, 2016

Status Verified

July 1, 2016

Enrollment Period

2.7 years

First QC Date

May 27, 2016

Last Update Submit

July 27, 2016

Conditions

Keywords

suppression mnemonicemotional responseinhibitory control of failuresneurological alterations

Outcome Measures

Primary Outcomes (1)

  • Blood Oxigen Level Dependent (BOLD) response as measured with fMRI

    1 hour

Study Arms (2)

patients with obsessive compulsive disorder

EXPERIMENTAL

Functional magnetic resonance imaging behavioral measures physiological measurements

Other: Functional magnetic resonance imagingBehavioral: behavioral measuresOther: physiological measurements

healthy participants

EXPERIMENTAL

Functional magnetic resonance imaging behavioral measures physiological measurements

Other: Functional magnetic resonance imagingBehavioral: behavioral measuresOther: physiological measurements

Interventions

healthy participantspatients with obsessive compulsive disorder
healthy participantspatients with obsessive compulsive disorder
healthy participantspatients with obsessive compulsive disorder

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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
  • 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 :
  • +1 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

GIP Cyceron

Caen, Calvados, 14000, France

Location

MeSH Terms

Conditions

Obsessive-Compulsive Disorder

Condition Hierarchy (Ancestors)

Anxiety DisordersMental Disorders

Study Officials

  • Anaïs Vandevelde, MD

    University Hospital, Caen

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 27, 2016

First Posted

August 1, 2016

Study Start

July 1, 2016

Primary Completion

March 1, 2019

Study Completion

December 1, 2019

Last Updated

August 1, 2016

Record last verified: 2016-07

Locations