- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00842413
Investigating the Role of the Premotor Cortex in Higher Cognitive Functions
February 11, 2009 updated by: Assistance Publique - Hôpitaux de Paris
What Part Does the Premotor Cortex Play in Subjective Visual Perception and in the Perception of Others' Actions?
This project aims at understanding better the role of the frontal lobe of the brain in our capacity to perceive visual information consciously, and also, in our capacity to perceive others' actions.
It includes a test where we ask subjects to detect visual information in front of a computer screen, and another test where we ask them to imitate finger movements.
Study Overview
Status
Terminated
Conditions
Detailed Description
This project is a twofold exploration of the functions of the premotor cortex, concerning, on the one hand, its role in conscious visual perception, and on the other hand, the part it may play in the perception and imitation of other people's movements.
Healthy subjects will be compared with subjects suffering from focal lesions within the premotor cortex, on two tasks: in the first task, the subjects will have to make a decision concerning the absence or presence of a visual item in their field of vision.
They will make (virtual) bets based on the subjective certainty of their perceptions - they will be told that these bets are purely virtual, and will not result in any financial gain or loss.
This study will help us understand the contribution of the prefrontal cortex to subjective weighing of perceptual certainty.
In the second task, the subjects will imitate a finger movement, based either on a fixed picture, or on a short motion picture.
Previous studies have shown that whether the movement is copied from a fixed picture or a moving picture changes reaction times and types of mistakes.
Neuroimaging studies have shown that a premotor area is involved in this effect.
The comparison of brain-damaged and healthy subjects will tell us what exactly the contribution of the prefrontal consists in.
Study Type
Observational
Enrollment (Actual)
9
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Paris, France, 75013
- Hôpital de la Pitié-Salpêtrière
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The visual pereption of subjects willl be studied, but no attempt will be made at modifying it, or treating any problem that they might have.
Description
Inclusion Criteria:
- Healthy subjects chosen from a pool of adult subjects, recruited through ads.
- In the second group, the subjects are recruited from a pool of brain-damaged patients treated at the hospital de la Pitié-Salpétrière. They must suffer from a focal lesion in the prefrontal cortex.
Exclusion Criteria:
- For the healthy group: any previous brain-related medical history.
- Widespread brain-damage, extending beyond the prefrontal cortex, that is to say, lesions that are not really focal.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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1
The study compares brain-damaged patients with healthy ones on two psychophysical tasks.
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The study does not intervene on the brain-damaged patients, it merely compares their behaviour with that of healthy patients on a range of psychophysical tasks.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Richard Levy, MD, Assistance Publique - Hôpitaux de Paris
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2007
Primary Completion (Actual)
September 1, 2007
Study Completion (Actual)
September 1, 2007
Study Registration Dates
First Submitted
February 11, 2009
First Submitted That Met QC Criteria
February 11, 2009
First Posted (Estimate)
February 12, 2009
Study Record Updates
Last Update Posted (Estimate)
February 12, 2009
Last Update Submitted That Met QC Criteria
February 11, 2009
Last Verified
November 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P060605
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.