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Recruiting NCT04279158

NCT04279158 Attention Modulation of Local and Global Inhibition Mechanisms

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Clinical Trial Summary
NCT ID NCT04279158
Status Recruiting
Phase
Sponsor Hospices Civils de Lyon
Condition Optical Phenomena
Study Type INTERVENTIONAL
Enrollment 120 participants
Start Date 2022-11-26
Primary Completion 2031-11-26

Eligibility & Interventions

Sex All sexes
Min Age 8 Years
Max Age 75 Years
Study Type INTERVENTIONAL
Interventions
experience 1 "The negative priming task"experience 2 "Stop signal task"experience 3 "Anti-saccades"

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 120 participants in total. It began in 2022-11-26 with a primary completion date of 2031-11-26.

⚠ 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

Human behavior is both flexible and adapted to the environmental context through inhibition capabilities; the investigator control the subject's behavior by repressing inappropriate responses and selecting, among several possibilities, those that are appropriate. These mechanisms are not independent of attentional control. Attention acts as a selection filter for the investigator's behavior. This leads us to hypothesize that attention modulates the mechanisms of inhibition. Nevertheless, the different brain structures involved, as well as mechanisms underlying the interaction between inhibition and attention remain largely unknown. Previous research has suggested that inhibition requires selective attention and, conversely, attentional mechanisms would result in the "deselection", or inhibition, of objects in space or irrelevant actions. Reconciling the literature on attention with the one on inhibition appears fundamental for the understanding of the instance to which the mechanisms of inhibition and the cognitive processes interact. Therefore, the goal of this research project will be to investigate how inhibition mechanisms are implemented in the brain and, in more detail, what determines the type of resulting inhibitory control: spatially localized or global. The investigator will test 3 different patient groups (optic ataxia, hemispatial neglect and attention-deficit hyperactivity disorder) compared to control. In conclusion, this research project will aim to develop a theoretical model of the interaction between attentional control and inhibition mechanisms in order to improve diagnostic and rehabilitation tools in the future.

Eligibility Criteria

All patients and healthy subjects: Inclusion Criteria: * male and female, age from 18 to 75 years included * normal vision or corrected vision * covered by social security * signed written informed consent Exclusion Criteria: * unable to comply with requirements of the study (neurological, psychiatric, sensory or motor troubles) * adults under legal protection Patient with hemispatial neglect: Inclusion Criteria: * After a stroke (\> 1 month ago), presence of a neurological impairment documented by brain imaging (standard of care) and by clinical symptoms. * The diagnosis will be dissociated from hemianopia by perimetry. The hemispatial neglect consists of a lack of perception and responsiveness concerning the controlesional visual hemifield. Patient with optic ataxia: * After a stroke (\> 1 month ago), presence of neurological injury in parietal cortex only, supported by a standard of care cerebral MRI * Present optic ataxia symptoms (The OA consists of pointing errors with the hand contralateral to the lesion (hand effect) and / or to visual targets presented in the field contralateral to the lesion (field effect)). Patient (adult and children) with attention-deficit hyperactivity disorder: * present a diagnosis of ADHD subtype inattention or impulse / hyperactivity as established by a neuropsychologist. * Children will be between 8 and 18 years old * Adults will be between 18 and 75 years old. * Participants will not report any comorbid learning disabilities to ADHD. For minors: \- Having obtained the written consent of the legal representative(s) Healthy subjects Inclusion Criteria: \- no known neurological injury

Contact & Investigator

Central Contact

Laure PISELLA, PhD

✉ laure.pisella@inserm.fr

📞 4 72 91 34 05

Principal Investigator

Laure PISELLA

PRINCIPAL INVESTIGATOR

Centre de recherche de Neurosciences de Lyon (CRNL)

Frequently Asked Questions

Who can join the NCT04279158 clinical trial?

This trial is open to participants of all sexes, aged 8 Years or older, up to 75 Years, studying Optical Phenomena. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04279158 currently recruiting?

Yes, NCT04279158 is actively recruiting participants. Contact the research team at laure.pisella@inserm.fr for enrollment information.

Where is the NCT04279158 trial being conducted?

This trial is being conducted at Bron, France.

Who is sponsoring the NCT04279158 clinical trial?

NCT04279158 is sponsored by Hospices Civils de Lyon. The principal investigator is Laure PISELLA at Centre de recherche de Neurosciences de Lyon (CRNL). The trial plans to enroll 120 participants.

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