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Recruiting NCT07145970

NCT07145970 Standardization of Spatial Neglect Assessment Tests

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Clinical Trial Summary
NCT ID NCT07145970
Status Recruiting
Phase
Sponsor Assistance Publique - Hôpitaux de Paris
Condition Perceptual Disorders
Study Type INTERVENTIONAL
Enrollment 210 participants
Start Date 2026-01-07
Primary Completion 2027-01-07

Eligibility & Interventions

Sex All sexes
Min Age 20 Years
Max Age 89 Years
Study Type INTERVENTIONAL
Interventions
Neuropsychological assessment tests for spatial neglect

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 210 participants in total. It began in 2026-01-07 with a primary completion date of 2027-01-07.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

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 spatial neglect. The norms correspond to the results obtained in a population free of any disorder that could have an impact on test performance. These results can vary in a normal, non-pathological way, with certain parameters such as age, sex, laterality or level of education. Defining these norms in healthy volunteers is therefore essential for interpreting results in patients suspected of spatial neglect, and in particular for defining pathological thresholds above which the diagnosis of spatial neglect can be retained. To answer the research question, we plan to include 210 people with no central neurological disease (stroke, epilepsy and multiple sclerosis in particular), in a single-center study in the neurovascular department of the Raymond-Poincaré hospital (Garches). The 210 subjects will be divided into 10-year age groups, from 20 to 89 years, with the recruitment of 30 participants per age group (15 men and 15 women): 20-29 years, 30-39 years, 40-49 years, 50-59 years, 60-69 years, 70-79 years, 80-89 years.

Eligibility Criteria

Inclusion Criteria: 1. Healthy volunteer attending the neurovascular department of Raymond-Poincaré Hospital 2. Aged between 20 and 89 years 3. Affiliated with a health insurance scheme 4. French-speaking 5. Has freely and knowingly expressed their non-opposition Exclusion Criteria: 1. Known history of central neurological disease: stroke (ischemic or hemorrhagic), transient ischemic attack, encephalitis, multiple sclerosis, or epilepsy. 2. 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). 3. 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. 4. Abnormal neurological examination: 1. National Institutes of Health Stroke Scale (NIHSS) score \> 0 2. Pyramidal reflex syndrome (hyperactive deep tendon reflexes with extended reflexogenic zones and spread). 5. Use of substances (alcohol or drugs) within 24 hours prior to the assessment. 6. Presence of cognitive or psychiatric disorders, assessed during the inclusion interview and neurological examination, at the examiner's discretion. 7. Language barrier or aphasia, assessed during the inclusion interview and neurological examination, at the examiner's discretion. 8. Participant under legal protection (guardianship, curatorship, or legal safeguard).

Contact & Investigator

Central Contact

Jean-Baptiste BRUNET de COURSSOU, Dr

✉ jean-baptiste.brunet-de-courssou@aphp.fr

📞 +33 1 47 10 72 55

Frequently Asked Questions

Who can join the NCT07145970 clinical trial?

This trial is open to participants of all sexes, aged 20 Years or older, up to 89 Years, studying Perceptual Disorders. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07145970 currently recruiting?

Yes, NCT07145970 is actively recruiting participants. Contact the research team at jean-baptiste.brunet-de-courssou@aphp.fr for enrollment information.

Where is the NCT07145970 trial being conducted?

This trial is being conducted at Garche, France.

Who is sponsoring the NCT07145970 clinical trial?

NCT07145970 is sponsored by Assistance Publique - Hôpitaux de Paris. The trial plans to enroll 210 participants.

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