Dysfunctions and Plasticity Mechanisms of Motor System Assessed by Cortico-cortical and Cortico-muscular Coherence Analysis in Amyotrophic Lateral Sclerosis
NCT ID: NCT01959373
Last Updated: 2015-08-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
SUSPENDED
NA
30 participants
INTERVENTIONAL
2013-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The main objective of our study project is to evaluate a new method assessing functional changes in motor system in ALS patients. By using cortico-muscular and cortico-cortical coherences, it could be possible to show modifications in both cortico-muscular relationship and in cortical activity coordination which could be related to clinical state in ALS patients. We notably expect a decrease in cortico-muscular coherence in ALS patients. Furthermore, these analyses could provide new insights in motor system plasticity phenomena. We expect a partial covering of voluntary motor command by cortical areas adjacent to primary motor cortex. Lastly, the hypothesis that an increased proportion of voluntary motor control may be assumed by ipsilateral corticospinal tract could be tested by coherence analyses.
Coherence analysis might be a useful method to detect corticospinal tract dysfunctions. This method has the advantage to be painless and not to use artificial stimulations as it is used in TMS.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Brain Excitability and Connectivity in Sensory-motor Pathways in ALS
NCT03694132
Study of Cognitive and Emotional Disorders in Amyotrophic Lateral Sclerosis
NCT01530438
Acoustic and Perceptual Markers of Dysarthria in Amyotrophic Lateral Sclerosis (ALS)
NCT03560661
Motor Asymmetry in Progressive Multiple Sclerosis Patients
NCT04918225
Evaluation of the Visual Motor Task's Impact on the Behavior of a Neuronal and Spinal Network in Hemiplegic Patients
NCT03094572
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
patients
electroencephalograms (EEG)
electro-myography (EMG)
healthy volunteers
electroencephalograms (EEG)
electro-myography (EMG)
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
electroencephalograms (EEG)
electro-myography (EMG)
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patien with a diagnosis of amyotrophic lateral sclerosis according to the El Escorial criteria of Brooks et al. 1994
* Patient , the beginning of the SLA date less than 12 months,
* Patient not having a familial form of ALS,
* Patient not having cancer, autoimmune disease, liver failure, severe hypertension or untreated, severe conduction disorders or uncontrolled arrhythmia
* Patient not having a chronic psychiatric disease, dementia.
* Patient with normal visual function
* Patients receiving social coverage
* Patient have read, understood and signed an informed consent after information
Exclusion Criteria
* Patient with a familial form of ALS,
* Patient associated with severe progressive disease (cancer, autoimmune disease , liver failure )
* Patient (s) with chronic mental illness, dementia ,
* Presence of atypical clinical signs such as cerebellar ataxia , extrapyramidal signs, sensory disorders , autonomic dysfunction .
* Clinical signs of chronic respiratory failure or slow and / or forced less than 70% of the theoretical value or chronic hypercapnia than 45 mmHg vital capacity .
* Patient private freedom following a judicial or administrative decision
* Patient major Trust
* Pateinte pregnant, parturient , lactating
* Patient major in legal protection ( guardianship )
* Pateinte pregnant , parturient , lactating
* Patient hospital without consent
* Patient admitted in a health or social establishment for purposes other than research
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Assistance Publique Hopitaux De Marseille
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
LOIC MONDOLONI
Role: STUDY_DIRECTOR
Assistance Publique Hopitaux De Marseille
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Assistance Publique Hopitaux de Marseille
Marseille, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2013-22
Identifier Type: OTHER
Identifier Source: secondary_id
2013-A00802-43
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.