Actively Recruiting

Age: 18Years - 70Years
All Genders
ID04182087

Cognitive Function Assessment in Patients With Focal Brain Injury

Led by University Hospital, Grenoble · Updated on 2024-01-17

400

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University Hospital, Grenoble

Lead Sponsor

G

Grenoble Institut des Neurosciences

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research focuses on studying cognitive difficulties linked to specific brain injuries and their locations. The aim is to build a large database of patient behavioral responses during cognitive tasks to better understand brain function. The study includes patients with focal brain lesions caused by stroke or surgical removal of brain tissue, which affect functions like attention, language, memory, decision-making, and executive function. Participants will undergo cognitive tasks that assess various higher brain functions such as attention, language, memory, decision-making, and executive skills. These tasks are observational and involve patients who have had focal brain injuries either from stroke or brain surgery. The study collects data during routine visits scheduled at 3, 6, 12, or 24 months after the brain lesion, with up to four sessions lasting about two hours each. During the study, participants will perform cognitive tasks while their behavioral performance, including reaction times and error rates, is recorded. These assessments happen during routine follow-up visits over two years. Researchers will analyze this data to explore links between brain structures and cognitive functions. The total participation may involve up to four sessions, each lasting approximately two hours, to track changes over time and better understand cognitive deficits after brain injury.

CONDITIONS

Brief Title

Cognitive Function Assessment in Patients With Focal Brain Injury

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male and female patients aged 18 to 70 years
  • A single, focal brain lesion confirmed by MRI, due to stroke or surgical removal
  • Intellectual ability sufficient to understand and perform cognitive tasks
Not Eligible

You will not qualify if you...

  • Patients deprived of liberty
  • Presence of a physical condition likely to affect cognitive abilities
  • Pregnant or nursing women

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)

Long-term Monitoring

Duration - Up to 24 months post lesion

Participants complete cognitive tasks assessing attention, language, memory, decision-making, and executive functions during routine visits over two years following their brain injury.

Up to 4 routine visits at 3, 6, 12, or 24 months post lesion, each lasting about two hours

Trial Site Locations

Total: 1 location

1

University Hospital, Grenoble

Grenoble, France, 38043

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Research Team

P

Philippe Kahane, MD, PhD

J

Julien Bastin, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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https://pubmed.ncbi.nlm.nih.gov/27527825