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Recruiting NCT05843604

Cerebral and Cognitive Markers of Treatment Resistance in Obsessive Compulsive Disorder

Observational OCD

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Functional MRI.
Who it may be relevant to
Registry conditions: OCD. Basic parameters: 18 years — 70 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Cerebral and Cognitive Markers of Treatment Resistance in Obsessive-compulsive Disorder: Towards Personalization of Patient Care

Overview

This study aims to define individual profiles of treatment resistants in order to find indicators and predictors of the therapeutic response.

Interventions

  • Other Functional MRI
    Three cognitive tests will be performed in the MRI, namely a stroop task, an N-back task and a switching task

Primary outcome measures

  • Cerebral activity modification during N-back task [Time frame: Day 1]
  • Cerebral activity modification during Stroop task [Time frame: Day 1]
  • Cerebral activity modification during switching task (Monsell et Mizon task ) [Time frame: Day 1]

Eligibility criteria

Inclusion criteria

  • Obsessive compulsive disorder diagnosed according to Diagnostic and Statistical Manual 5 criteria (patients will be included regardless of the severity and resistance of their pathology and their levels of executive functions)
  • Understand and accept the constraints of the study
  • Be a beneficiary or affiliated to a Health Insurance scheme

Exclusion criteria

  • Present one of the diagnoses according to the criteria of the DSM 5: schizophrenic disorders, substance abuse or dependence to a substance according to the criteria of the M.I.N.I. version 5.0 (Sheehan et al., 1998)
  • Generalized anxiety disorder, social anxiety, nicotine dependence and history of a major depressive episode are not exclusion criteria according to the M.I.N.I. version 5.0 (Sheehan et al., 1998)
  • Have a serious intercurrent pathology
  • Being a pregnant woman
  • Being a woman of childbearing age without effective contraception.
  • Being hospitalized under duress or on an outpatient basis in a care program
  • Being under judicial protection (reinforced curatorship, guardianship)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

France · 1 center
  • Centre Hospitalier Henri Laborit — Poitiers

Identifiers

NCT: NCT05843604 · 2022-A00463-40

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗