Actively Recruiting
Movement Error-processes and Sensorimotor Adaptation in Parkinsonian Patient
Led by Assistance Publique Hopitaux De Marseille · Updated on 2024-01-05
100
Participants Needed
1
Research Sites
430 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of the present project is to document the relationship between the behavioral deficits and the electrophysiological anomalies observed in PD patients in tasks involving motor adaptation to visual or mechanical perturbations.
CONDITIONS
Official Title
Movement Error-processes and Sensorimotor Adaptation in Parkinsonian Patient
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient aged over 18 years
- Right-handed patients according to the Modified Edinburgh Handedness Inventory
- Patient with Parkinson's disease according to Gibb criteria
- Idiopathic Parkinson's Disease with a history of more than 5 years
- Stimulation electrodes implanted in both subthalamic nuclei
- Dopa-sensitivity greater than 50%
- Absence of signs of cognitive impairment
- Patient agreed to participate and signed informed consent
- Patient affiliated with a health insurance
You will not qualify if you...
- Person unlikely to participate in the entire study
- Pregnant or likely to be pregnant during the year
- Patients unable to give informed consent (e.g., detainees, adults under guardianship)
- Person unable to understand the nature and purpose of the study or with comprehension difficulties that could affect study conduct
- Person refusing to sign the informed consent form
- Person able to consent but unable to read/write French
- Patient unable to participate in an MRI study according to specified criteria
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Service de Neurologie, Hôpital de la Timone, Assistance Publique Hôpitaux de Marseille
Marseille, France, 13005
Actively Recruiting
Research Team
A
Alexandre EUSEBIO, MD, PHD
CONTACT
C
Camille DELANNOY
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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