Functional Magnetic Resonance Imaging (fMRI) Study of Memory in Children
- Conditions
- Childhood Absence Epilepsy [Pyknolepsy]
- Registration Number
- NCT00242905
- Lead Sponsor
- Assistance Publique - Hôpitaux de Paris
- Brief Summary
Memory is a cognitive function whose development is still poorly documented in children, but which is often disturbed in temporal epilepsy. There are no studies about the disorders of episodic memory. The investigations using functional MRI (fMRI) are scarce, they do not involve this field and none are dedicated to children. The objectives of this project are to study the neuronal networks involved in episodic memory in normal children, as well as the disorders of episodic memory in children with epilepsy and the mechanisms of cognitive and cerebral reorganization in epilepsy.
- Detailed Description
Twenty children aged from 6 to 18 years with temporal and/or frontal epilepsy and 20 normal children in the same age range will undergo the following examinations in a unique day in the Unit Hospital F. JOLIOT(CEA in ORSAY, France):
1. complete neuropsychological evaluation including episodic memory,
2. structural MRI to quantify, using VBM, the potential abnormalities of the anatomical structures, to perform cognitive-morphological correlations, and to localize the neuronal networks activated on fMRI,
3. functional MRI using an original task of episodic memory, specifically dedicated to children and being under behavioural validation laboratory.
The analysis of fMRI data will be performed using SPM and taking into account the existence of epilepsy or not, of cerebral lesion or not, age, handedness, the side and location of epileptogenic focus, the age of seizure onset, and the type of antiepileptic treatment.
This study has been approved by the Ethic Committee in september 2004 (CCPPRB BICETRE, promotion of ASSISTANCE PUBLIQUE - HOPITAUX de PARIS).
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 52
- Parents or legal tutors of the children having given written consent to participate to the study, after having being fully informed.
- Patients presenting with a temporal and/or frontal epilepsy and being able to perform the tasks of the protocol.
- Controls being recruited among brothers, sisters, and friends of the patients and being right-handlers, without any neurological history or learning disorders.
- Any contra-indication to MRI or being claustrophobia or blind.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (2)
Service Hospitalier Frédéric Joliot (SHFJ)
🇫🇷Orsay, France
Necker Hospital
🇫🇷Paris, France