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Recruiting NCT07191197

How do Patients With Amnesia Acquire New Knowledge?

No phase Interventional Amnesia Memory Disorder

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: MRI, Psychometric.
Who it may be relevant to
Registry conditions: Amnesia, Memory Disorder. 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

New Semantic Learning in Patients With Selective Brain Lesions in Temporal Regions: a Behavioural and MRI Study

Overview

THE STUDY AIMS to constitute the largest group of patients with major memory impairment resulting from various etiology and specific lesions of the medial temporal lobe (MTL) and use a combined psychometric and neuroimaging approach to study the factors allowing these patients to successfully learn new semantic information.

Detailed description

The preservation of learning abilities is an essential aspect in the implementation of cognitive rehabilitation programs for patients with an amnesic syndrome. Particularly disabled on a daily basis, these patients have significant difficulties in coping with the demands of work and family life. Data from previous case studies attest to the ability of these patients to rely on preserved cognitive systems to learn new semantic information. However, the procedures for the acquisition of new information are sometimes long, not optimal and the clinical factors, that can influence it, are poorly identified. In addition, the brain networks necessary for such learning are still debated. In order to better understand the cognitive mechanisms and brain networks that underlie the ability to learn new semantic information, the research aims to study a group of patients with major memory impairment following medial temporal lobe lesions of various etiologies (non-degenerative). The study will use a combined psychometric and neuroimaging approach to identify the factors that enable these patients to successfully learn new semantic information.

Interventions

  • Other MRI
    structural and functional resting state MRI
  • Other Psychometric
    2 cognitive research tasks of semantic learning and neuropsychological assessment

Primary outcome measures

  • Performance on Fast-Mapping semantic learning task [Time frame: Baseline]
Secondary outcome measures (1)
  • Performance of semantic learning [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • Patients aged between 18 and 70 years
  • Living in France since less than 20 years, being able to understand the French language, and have basic cultural knowledge as evaluated in classical clinical consultation
  • Written agreement to participate in the study
  • Intellectual capacities compatible with the cognitive tasks and signing of consent
  • Affiliation to the French social security system
  • For patients: bilateral brain lesion of the medial temporal lobe or the extended hippocampal system

Exclusion criteria

  • Subjects under the age of 18 or over 70
  • Contraindications for MRI (examples: wearers of a pacemaker or cardiac defibrillator, implanted equipment activated by an electrical, magnetic or mechanical system, wearers of haemostatic clips for intracerebral aneurysms or carotid arteries, wearers of orthopedic implants, claustrophobic)
  • Refusal to be informed of an anomaly detected during the MRI

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

Healthy volunteers: Yes

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

France · 2 centers
  • University Hospital of Caen — Caen
  • University Hospital of Toulouse — Toulouse

Identifiers

NCT: NCT07191197 · RC31/23/0377

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗