Dysfunctions and Plasticity Mechanisms of Motor System Assessed by Cortico-cortical and Cortico-muscular Coherence Analysis in Amyotrophic Lateral Sclerosis

NCT01959373 | Suspended

• 2 other identifiers: 2013-A00802-432013-22
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 1

Brief Summary

Amyotrophic lateral sclerosis (ALS) is characterized clinically by abnormalities of both upper motor neurons (UMN) and lower motor neurons (LMN). The presence of UMN signs is not always easy to establish. The only technique used in routine to assess the corticospinal dysfunctions is based on transcranial magnetic stimulation (TMS). However, this technique is largely dependent on LMN state and is based on artificial motor cortex activation. 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.

Conditions

Amyotrophic Lateral Sclerosis

Outcome Measures

Primary Outcomes (1)

• recording neuronal activities

  simultaneous recording of brain activity using electrodes attached to the scalp and muscle activities of muscles of the hands with electrodes bonded to the skin.

  12 months

Secondary Outcomes (1)

• identify plasticity phenomena

  12 months

Study Arms (2)

patients

EXPERIMENTAL

Procedure: electroencephalograms (EEG); Procedure: electro-myography (EMG)

healthy volunteers

EXPERIMENTAL

Procedure: electroencephalograms (EEG); Procedure: electro-myography (EMG)

Interventions

electroencephalograms (EEG) PROCEDURE

healthy volunteers; patients

electro-myography (EMG) PROCEDURE

healthy volunteers; patients

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patient female or male, more than 18 years,
• 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

You may not qualify if:

• Patient minor
• 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

Sponsors & Collaborators

• Assistance Publique Hopitaux De Marseille: lead

Study Sites (1)

Assistance Publique Hopitaux de Marseille

Marseille, 13354, France

Location

MeSH Terms

Conditions

Amyotrophic Lateral Sclerosis

Condition Hierarchy (Ancestors)

Spinal Cord Diseases; Central Nervous System Diseases; Nervous System Diseases; Motor Neuron Disease; Neurodegenerative Diseases; TDP-43 Proteinopathies; Neuromuscular Diseases; Proteostasis Deficiencies; Metabolic Diseases; Nutritional and Metabolic Diseases

Study Officials

• LOIC MONDOLONI

  Assistance Publique Hopitaux De Marseille

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: DIAGNOSTIC
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 8, 2013
• First Posted: October 10, 2013
• Study Start: October 1, 2013
• Primary Completion: July 1, 2014
• Last Updated: August 24, 2015

Record last verified: 2015-08

Locations

FR (1)