ATENA-F: Anterior Temporal Epilepsy Neuropsychological Assessment of Faces

Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Unknown status
CT.gov ID
NCT02888925
Collaborator
(none)
80
1
2
79
1

Study Details

Study Description

Brief Summary

The purpose is to evaluate neuropsychological effects of anterior temporal epilepsy in face perception by comparison of performances of epileptic patients and control individuals, sex-, age- and socio-educational level-matched.

Secondary purposes are to prospectively evaluate neuropsychological impact of anterior temporal lobectomy performed for surgical treatment of anterior temporal epilepsy on face perception (exploratory study).

Condition or Disease Intervention/Treatment Phase
  • Other: Mooney test
  • Other: Benton Face Recognition test
  • Other: Face inversion effect test
  • Other: Face composite effect test
  • Other: Cambridge Face Memory Test
  • Other: Matching different view test
  • Other: Memorizing and recognition of new faces test
  • Other: Memorizing and recognition of new objects test
  • Other: Recognition of celebrities and access to semantic information test
  • Procedure: Lobectomy
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Evaluation of Neuropsychological Effects of Drug-resistant Anterior Temporal Epilepsy and Anterior Temporal Lobectomy in Face Perception
Actual Study Start Date :
Aug 1, 2013
Actual Primary Completion Date :
Sep 1, 2017
Anticipated Study Completion Date :
Mar 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Other: Epilepsy

Patients do face specific tests during conventional pre-lobectomy intercritical assessment hospitalization (inclusion, day 0) and after 6 and 18 months from anterior temporal lobectomy

Other: Mooney test

Other: Benton Face Recognition test

Other: Face inversion effect test

Other: Face composite effect test

Other: Cambridge Face Memory Test

Other: Matching different view test

Other: Memorizing and recognition of new faces test

Other: Memorizing and recognition of new objects test

Other: Recognition of celebrities and access to semantic information test

Procedure: Lobectomy
In patients with anterior temporal epilepsy, at 6 to 12 months after inclusion, depending on surgery decision taken after pre-surgery conventional intercritical assessment

Other: Control

Control individuals do face specific tests during inclusion visit (day 0) and after X months (X = time from day 0 and lobectomy of matched patient + 6 months)

Other: Mooney test

Other: Benton Face Recognition test

Other: Face inversion effect test

Other: Face composite effect test

Other: Cambridge Face Memory Test

Other: Matching different view test

Other: Memorizing and recognition of new faces test

Other: Memorizing and recognition of new objects test

Other: Recognition of celebrities and access to semantic information test

Outcome Measures

Primary Outcome Measures

  1. Scores obtained with Benton test by patients with anterior temporal epilepsy and matched control individuals [day 0]

Secondary Outcome Measures

  1. Change of scores obtained with Benton test by epilepsy patients before and after lobectomy and control individuals (only patients having undergone anterior temporal lobectomy and matched control individuals) [day 0 and after 12 to 18 months]

  2. Change of scores obtained with Benton test by epilepsy patients before and after lobectomy and control individuals (only patients having undergone anterior temporal lobectomy and matched control individuals) [day 0 and after 24 to 30 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
ALL:
  • Informed consent

  • Affiliation to social security

  • Preliminary medical examination

PATIENTS WITH EPILEPSY:
  • Symptomatic drug-resistant anterior temporal epilepsy (confirmed with video-electroencephalography and magnetic resonance imaging and if necessary intracerebral SEEG exploration)

  • Patient needing anterior temporal lobectomy and undergoing pre-surgery conventional intercritical assessment for surgery decision

  • Nonverbal IQ ≥ 70 (WAIS-IV)

  • At least 6 successful VOSP tests (perception test)

Exclusion Criteria:
ALL:
  • persons under legal protection or incapable to consent

  • Persons deprived of liberty by juridical or administrative decision

PATIENTS WITH EPILEPSY:
  • Sever visual disorders of neurological or ophthalmological origin
CONTROL INDIVIDUALS:
  • Psychiatric or neurological disorders

  • Important ophthalmological disorders

Contacts and Locations

Locations

Site City State Country Postal Code
1 Service de Neurologie, Hôpital Central, CHU de Nancy Nancy France

Sponsors and Collaborators

  • Central Hospital, Nancy, France

Investigators

  • Principal Investigator: Louis Maillard, Service de Neurologie, Hôpital Central, CHU de Nancy, France

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT02888925
Other Study ID Numbers:
  • 2013-A00515-40
First Posted:
Sep 5, 2016
Last Update Posted:
Jul 24, 2019
Last Verified:
Jul 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 24, 2019