Actively Recruiting

Phase Not Applicable
Age: 20Years - 89Years
All Genders
Healthy Volunteers
ID07145970

Standardization of Spatial Neglect Assessment Tests in a Francophone Population

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2026-02-10

210

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying spatial neglect, a common cognitive disorder after stroke that causes difficulty in noticing stimuli on one side, often the left. This research aims to define standard test results for spatial neglect in healthy adults without neurological diseases, considering factors like age, sex, and education level. Establishing these norms is essential for accurately diagnosing spatial neglect in patients and understanding variations in normal populations. Participants will undergo four standardized paper-and-pencil tests for spatial neglect assessment, including the Apples Cancellation Test for visual neglect, the simplified Comb and Razor Test for personal and motor neglect, a blind line bisection test for tactile neglect, and a dot test for visual exploration. The tests use French-translated instructions, and the study plans to include 210 healthy French-speaking volunteers aged 20 to 89 years, divided into 10-year age groups with equal numbers of men and women. Participants will be assessed once during the study at the neurovascular department. Researchers will collect test scores and analyze them statistically to identify the influence of age, sex, occupational level, hand used, and laterality on test results and completion times. The primary outcome is the average score on the Apples Cancellation Test after 12 months. Secondary outcomes include average scores on the other tests at inclusion. This helps set reference standards to interpret spatial neglect assessments in patients.

CONDITIONS

Brief Title

Standardization of Spatial Neglect Assessment Tests

Who Can Participate

Age: 20Years - 89Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • 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 such as sensorimotor deficits, dysarthria, aphasia, blurred or double vision, or visual or sensory hallucinations
  • Significant visual impairment in near vision despite correction or monocular blindness preventing test target recognition
  • Abnormal neurological examination including NIHSS score greater than 0 or pyramidal reflex syndrome
  • Use of alcohol or drugs within 24 hours prior to assessment
  • Presence of cognitive or psychiatric disorders as assessed during inclusion
  • Language barrier or aphasia
  • Participant under legal protection such as guardianship, curatorship, or legal safeguard

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 1 day

Participants complete standardized neuropsychological assessments designed to evaluate different forms of spatial neglect using French-translated instructions.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 12 months

Researchers analyze test results to establish normative reference scores for healthy French-speaking adults based on age, sex, and professional qualification.

No visits; data analysis period

Trial Site Locations

Total: 1 location

1

CHU Raymond Poincarré

Garche, France, 92380

Actively Recruiting

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Research Team

J

Jean-Baptiste BRUNET de COURSSOU, Dr

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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