Image

Electrophysiological Evaluation of Voluntary Attention

Recruiting
18 - 80 years of age
Both
Phase N/A

Powered by AI

Overview

Aim : To assess the ability of healthy subjects and patients with a severe motor disability to voluntary control their attention

Material and Methods:

Population: healthy subjects, patients with brain injury Electroencephalographic study to research attentional modulation during different kind of stimulation (visual, auditory, tactile)

Sudy 1: passive recording.

Study 2: active recording (instruction of attentional control given to the subject).

Study 3: active recording with a feedback obtained after a processing of the brain activity.

Eligibility

Inclusion Criteria:

Inclusion criteria for patients :

  • Adults, man or woman, left or right-handed, from 18 years old to 80 years-old ;
  • Diagnosis :
    • Locked-in syndrome :
        < Brainstem injury, without any evolution for at least 3 week, etiology : vascular,
        traumatic < Amyotrophic Lateral Sclerosis < Following damage to the central or peripheral
        nervous system
          -  Or Minimal conscious state or Unresponsive Wakefulness Syndrome consecutive to a
             severe acquired brain injury for at least one month
          -  Or with a severe brain injury, since birth or acquired, for at least one month
          -  Or with Guillain-Barré syndrome
               -  Subjects affiliated to social security;
               -  Signature of consent form by the patient or by a relative (family member or "the
                  trusted person") if obtaining a consent is impossible
        Inclusion criteria of Healthy subjects
          -  Adults, man or woman, left or right-handed, from 18 years old to 80 years-old ;
          -  Without known auditory impairment
          -  Subjects able to understand the experimental instructions
          -  Subjects affiliated to social security;
          -  Signature of consent form
        Exclusion criteria of patients and healthy subjects
          -  Medical history : psychiatric disorders (except if due to brain injury), neurologic
             disorders (except if due to brain injury)
          -  For healthy subjects : history of brain injury
          -  Pregnant women or breastfeeding women
          -  Person under legal protection
          -  Medico-legal conflicts
          -  Absence of consent by the subject or the patient or his/her representant

Study details

Brain Injury

NCT02567201

Hospices Civils de Lyon

26 January 2024

Step 1 Get in touch with the nearest study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.