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NCT07295652Recruiting

Characterization of High-Level Cognitive Impairments in Patients With Neuropsychiatric Disorders

Source: ClinicalTrials.gov · Last updated 19 Dec 2025

Brief summary (registry, in English)

Neuropsychiatric disorders are extremely common, severe, and disabling conditions. In the field of psychiatry, they notably include schizophrenia, mood disorders (depressive and bipolar disorders), autism spectrum or neurodevelopmental disorders, obsessive-compulsive disorder, eating disorders, and personality disorders. In the field of neurology, one can cite neurodegenerative diseases (such as Alzheimer's disease, but also frontotemporal dementia or Parkinson's disease, which often represent frequent and challenging differential diagnoses of psychiatric disorders), focal neurological lesions (notably strokes and tumors), or epilepsy. Cognitive impairments are present in nearly all neuropsychiatric disorders and contribute significantly to disability. While impairments in working memory and attention, executive functions, and social cognition have been relatively well studied, other cognitive domains remain largely unexplored in these populations. This is particularly the case for various aspects of motivation, metacognition, conscious access, or causal (Bayesian) inference. Although these domains likely play an important role in prognosis, no consensus currently exists regarding the methods for evaluating these functions. The main objective of this study is to define a multidimensional, transdiagnostic atlas of high-level cognitive impairments-both specific and shared-across severe psychiatric disorders (notably schizophrenia, depressive disorder, bipolar disorder, autism spectrum or neurodevelopmental disorders, and obsessive-compulsive disorder) and neurological disorders (notably neurodegenerative diseases, focal neurological lesions, and epilepsy), by comparing them to healthy volunteers. The investigators also aim to investigate the progression of cognitive impairments over time, across different phases of illness (symptom stabilization or exacerbation) or therapeutic intervention, through longitudinal follow-up of patients being monitored within the recruiting center. Finally, in a more exploratory manner, the investigators aim to investigate the neural correlates of the identified cognitive impairments.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
600 (estimated)
First submitted
13 Jun 2025
Start date
12 Mar 2024
Primary completion date
31 Mar 2039
Lead sponsor
Centre Hospitalier St Anne
NCT number
NCT07295652

What you commit to

  • Study type: Interventional
  • Planned participants: 600
  • From 12 Mar 2024 to the primary completion date, 31 Mar 2039
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Current diagnosis of a psychiatric disorder according to ICD-10 (F20-F98) or current prescription of a psychotropic medication, or diagnosis of a neurological disorder according to ICD-10 (G00-G99)
  • History of depression (F32)
  • Substance use disorder (excluding tobacco)
  • Neurological history (e.g., stroke, coma, epilepsy, neuroinflammatory or neurodegenerative disease) or identified cognitive disorder
  • Inability to complete cognitive testing (e.g., due to motor or sensory impairment)
    • For participants undergoing MRI (without contrast agent):
  • Presence of MRI contraindications: non-MRI-compatible pacemaker, heart valve, implant, or metallic foreign body

Other

  • For healthy volunteers:
  • Pregnancy at the time of MRI

Who the study is looking for

  • For patients:
  • Aged over 18 years
  • Diagnosed with a psychiatric disorder according to ICD-10 by a psychiatrist (F10-F98) or diagnosed with a neurological disorder according to ICD-10 by a neurologist (G00-G99)
  • Provided written informed consent
  • Affiliated with a social security scheme
    • For healthy volunteers:
  • Aged over 18 years
  • Provided written informed consent
  • Affiliated with a social security scheme

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hopital Fondation Adolphe de Rothschild
Coordinator of this site? Confirm its status
ParisFranceNot yet recruiting
Departement of Adult Psychiatry, GH Pitié Salpétrière
Coordinator of this site? Confirm its status
ParisFranceRecruiting
- Groupe hospitalo-universitaire Paris Psychiatrie et Neurosciences
Coordinator of this site? Confirm its status
ParisFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.