ClinicalTrials.Veeva

Menu

Neural Bases of Post-stroke Emotion Perception Disorders (STROKEM)

U

University Hospital, Lille

Status

Enrolling

Conditions

Stroke
Stroke Sequelae
Emotions

Study type

Observational

Funder types

Other

Identifiers

NCT05595005
2020-A00193-36 (Other Identifier)
2019_12

Details and patient eligibility

About

This monocentric physiological study will evaluate the neural bases of visual recognition of emotions in stroke patients vs. healthy controls using MRI (functional and structural connectivity) and EEG.

Full description

This monocentric physiological study will evaluate the neural bases of visual recognition of emotions in stroke patients vs healthy controls (2 groups of 40 subjects). It will include functional MRI, structural MRI (disconnectome), EEG, and behavioral assessments of emotion recognition and executive functions.

Enrollment

80 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Stroke group:

  • Man or Woman
  • Age 18-80y
  • Unique stroke, ischemic or hemorrhagic
  • at the chronic phase (< 6 months)
  • Written informed consent
  • subject having a social insurance
  • Subject who consent to complete all the study's experiments

Healthy controls group:

  • Man or Woman
  • Age 18-80y
  • No history of neurological or psychiatric disease.

Exclusion criteria

Stroke group

  • Subject who is unable to consent (due to dementia, severe aphasia, psychiatric disorder...)
  • History of other neurologic disorders
  • Significant le vel of depression or anxiety, assessed by the STAI and the BDI questionnaires
  • Non corrected visual loss
  • Subjects suffering from visual neglect (assessed by the Bells Test and a bisection test (20mm)
  • contra-indications to MRI
  • pregnant or breastfeeding woman
  • Women of childbearing age without effective contraception

Healthy controls group

  • Subject who is unable to consent (due to dementia, severe aphasia, psychiatric disorder...)
  • History of neurologic disorders
  • Significant level of depression or anxiety, assessed by the STAI and the BDI questionnaires
  • Non-corrected visual loss
  • contra-indications to MRI
  • pregnant or breastfeeding woman
  • Women of childbearing age without effective contraception

Trial design

80 participants in 2 patient groups

Stroke
Description:
Stroke patients (ischemic or hemorrhagic) in the chronic phase (\> 6 months)
Healthy controls
Description:
Healthy adult controls

Trial contacts and locations

1

Loading...

Central trial contact

Etienne Allart, MD, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems