Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06847152

Spatial Memory and Temporal Lobe Epilepsy

Led by Centre Hospitalier Metropole Savoie · Updated on 2025-09-22

37

Participants Needed

1

Research Sites

37 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Temporal lobe epilepsy (TLE) can cause memory disorders, including long-term forgetfulness due to a failure to consolidate verbal but also spatial information. The forgetting phenomenon presented by these epileptic patients is called accelerated forgetting in the literature and remains difficult to objectify during cognitive assessments. It is indeed particularly complicated to evaluate long-term spatial memory and to account for the topographical complaint, although recurrent, of patients with this TLE. A navigation task being proposed as part of the neuropsychological assessment of patients with a spatial memory complaint, it is interesting to study the performance pattern of patients with TLE by comparing them to a group of control subjects matched in age and gender in order to verify whether there is significant long-term forgetting and whether there is a significant difference between Right TLE and Left TLE. Indeed, several studies have demonstrated this accelerated long-term forgetting in epileptic patients (Cassel et al., 2016; Lemesle et al., 2017; Landry et al., 2022; Blake et al., 2020) but few with a retention delay of several weeks (Tramoni et al., 2009). This study allows us to statistically analyze the effects of these two groups: epileptic patients and healthy volunteers, but also to combine the effect of the laterality of epilepsy specifically on spatial memory performance.

CONDITIONS

Official Title

Spatial Memory and Temporal Lobe Epilepsy

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy volunteers aged over 18 years
  • Right-handed participants only
  • Free of known neurological diseases
  • Signed informed consent
  • Matched in age and gender with epileptic patients
  • Epileptic patients must be adults with temporal lobe epilepsy confirmed by EEG and/or MRI
  • Epileptic patients must have undergone neuropsychological assessment including the navigation task
  • Epileptic patients must be informed of the study and consent to data use
Not Eligible

You will not qualify if you...

  • Pregnant, parturient, or breastfeeding women
  • Persons deprived of judicial or administrative freedom
  • Persons under legal protection or unable to consent
  • Persons not affiliated to a social security scheme
  • Left-handed participants
  • Participants familiar with the hospital premises
  • Participants not speaking French
  • Patients who had epilepsy surgery between initial and follow-up visits
  • Volunteers with cognitive disorders based on pretest scores

AI-Screening

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Trial Site Locations

Total: 1 location

1

Centre Hospitalier Métropole Savoie

Chambéry, Savoie, France, 73011

Actively Recruiting

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Research Team

J

Jacqueline BOUCHET

CONTACT

F

Fabienne Prieur

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

2

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