Status:

NOT_YET_RECRUITING

Standardization of Spatial Neglect Assessment Tests

Lead Sponsor:

Assistance Publique - Hôpitaux de Paris

Conditions:

Perceptual Disorders

Healthy Volunteers

Eligibility:

All Genders

20-89 years

Phase:

NA

Brief Summary

Spatial neglect is a common cognitive disorder in stroke patients, characterized by a lateralized deficit in attention and intention. This research focuses on defining norms for tests to assess spati...

Detailed Description

Spatial neglect is a loss of attention to stimuli in the absence of sensory damage. It is most often a left egocentric hemineglect, due to involvement of the right perisylvian cortex, in which the pat...

Eligibility Criteria

Inclusion

  • Healthy volunteer attending the neurovascular department of Raymond-Poincaré Hospital
  • Aged between 20 and 89 years
  • Affiliated with a health insurance scheme
  • French-speaking
  • Has freely and knowingly expressed their non-opposition

Exclusion

  • Known history of central neurological disease: stroke (ischemic or hemorrhagic), transient ischemic attack, encephalitis, multiple sclerosis, or epilepsy.
  • Medical interview suggesting past central nervous system involvement: history of episodes such as sensorimotor deficits, dysarthria, aphasia, blurred or double vision, or positive symptoms such as visual or sensory hallucinations (e.g., paresthesias).
  • Significant visual impairment - as judged by the examiner - in near vision despite correction, or monocular blindness. Specifically, inability to distinguish the targets with gaps in the example (pre-test) of the Apples Cancellation Test.
  • Abnormal neurological examination:
  • National Institutes of Health Stroke Scale (NIHSS) score \> 0
  • Pyramidal reflex syndrome (hyperactive deep tendon reflexes with extended reflexogenic zones and spread).
  • Use of substances (alcohol or drugs) within 24 hours prior to the assessment.
  • Presence of cognitive or psychiatric disorders, assessed during the inclusion interview and neurological examination, at the examiner's discretion.
  • Language barrier or aphasia, assessed during the inclusion interview and neurological examination, at the examiner's discretion.
  • Participant under legal protection (guardianship, curatorship, or legal safeguard).

Key Trial Info

Start Date :

October 1 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

October 1 2026

Estimated Enrollment :

210 Patients enrolled

Trial Details

Trial ID

NCT07145970

Start Date

October 1 2025

End Date

October 1 2026

Last Update

August 28 2025

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