- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03103230
Electro-physiological Signs to Prognostic Aphasia Recovery After a Stroke (APHA-TMS)
Recherche de Marqueurs Pronostiques électro-physiologiques précoces Chez l'Aphasique après un Accident Vasculaire cérébral.APHA-TMS
Study Overview
Status
Intervention / Treatment
Detailed Description
• Background : Stroke affects approximately 130,000 people per year and communication disorders occur in 35% of cases, resulting in left brain damages. Aphasia is the main cause of these disorders. It is a sign of poor prognosis in the functional recovery after stroke. Recent studies have attempted to establish early clinical prognostic criteria to establish a predictive model of aphasia recovery. The issue of the possibility of prediction is important and can influence the rehabilitation treatment decided in the early days after stroke, with adequate guidance in rehabilitation structures.
There are close links between motor system and language, either at production or comprehension, and more particularly concerning the motricity of the hand or lips. The cortical excitability of motor areas of the right upper limb is thus modified by the language in healthy subjects, but also in the aphasic person.
- Purpose : The main: to study, among the aphasic person, if Motor Evoked Potentials (MEP) performed within the first 14 days after a stroke can predict a good recovery from aphasia 6 months of the initial episode.
- Detailed description: All aphasic stroke patients with ischemic or hemorrhagic damages will be proposed for inclusion. All patients will benefit in the acute phase of an aphasia evaluation, and a clinical evaluation. All patients will have a study of motor evoked potentials (abductor pollicis brevis and orbicularis oris) less than 14 days from stroke. The investigators will evaluate the aphasia 3 and 6 months after stroke, to determinate if MEP can predict a good recovery of aphasia.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Bordeaux, France, 33076
- CHU de Bordeaux
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- All patients with a left stroke (first clinical episode deficit) imaging confirmed.
- With aphasia (-1 language analysis in the acute phase and severity of the questionnaire LAST (Flamand-Roze, Falissard et al. 2011))
- Right-handed (Edinburgh Handedness Inventory)
- Free of dementia before stroke
- Older than 18 years
- French
- Able to hold a sitting in chair.
- Included in maximum 14 days after stroke
- Patient social security system
- Free Consent, informed writing signed by the participant or the person of confidence and the investigator (no later than the day of inclusion and before any examination required by research)
Exclusion Criteria:
- Refusal of the consent
- Impaired alertness
- Dementia prior to stroke
- Illiteracy
- Severe dysarthria
- Previous psychiatric history requiring hospitalization in a specialized environment for more than two months
- Pregnant
- Major visual or auditory perceptual disorder
- Previous epilepsy or seizures in hyperacute phase of stroke
- Treatment strongly interacting with GABAergic or glutamatergic system
- Contraindication to MEP: clip intracranial ferromagnetic pacemakers, cochlear implant, intracerebral stimulator.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Motor Evoked Potentials
Patients with aphasia after a stroke
|
Motor Evoked Potentials of lips and hand recorded after cortical magnetic stimulation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evolution of aphasia
Time Frame: 6 months after stroke
|
Aphasia Severity Rating Scale (ASRS)
|
6 months after stroke
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evolution of aphasia
Time Frame: 3 months after stroke
|
Aphasia Severity Rating Scale Score (ASRS)
|
3 months after stroke
|
|
Pattern of aphasia
Time Frame: 3 & 6 months after stroke
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Boston Diagnostic Aphasia Examination (BDAE) ;
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3 & 6 months after stroke
|
|
Pattern of aphasia
Time Frame: 3 & 6 months after stroke
|
Language Screening Test (LAST b)
|
3 & 6 months after stroke
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: GLIZE Bertrand, MD, University Hospital Bordeaux, France, EA 4136 Univ. Bordeaux, France
- Study Chair: PICAT Quitterie, MD, Unité de Soutien Méthodologique à la Recherche Clinique
Publications and helpful links
General Publications
- Dickey, L., A. Kagan, et al. (2010).
- El Hachioui, H., H. F. Lingsma, et al. (2013).
- Fadiga L, Craighero L, Buccino G, Rizzolatti G. Speech listening specifically modulates the excitability of tongue muscles: a TMS study. Eur J Neurosci. 2002 Jan;15(2):399-402. doi: 10.1046/j.0953-816x.2001.01874.x.
- Meister IG, Wilson SM, Deblieck C, Wu AD, Iacoboni M. The essential role of premotor cortex in speech perception. Curr Biol. 2007 Oct 9;17(19):1692-6. doi: 10.1016/j.cub.2007.08.064. Epub 2007 Sep 27.
- Meister IG, Sparing R, Foltys H, Gebert D, Huber W, Topper R, Boroojerdi B. Functional connectivity between cortical hand motor and language areas during recovery from aphasia. J Neurol Sci. 2006 Sep 25;247(2):165-8. doi: 10.1016/j.jns.2006.04.003. Epub 2006 Jun 5.
- Meister IG, Buelte D, Staedtgen M, Boroojerdi B, Sparing R. The dorsal premotor cortex orchestrates concurrent speech and fingertapping movements. Eur J Neurosci. 2009 May;29(10):2074-82. doi: 10.1111/j.1460-9568.2009.06729.x. Epub 2009 May 9.
- Tokimura H, Tokimura Y, Oliviero A, Asakura T, Rothwell JC. Speech-induced changes in corticospinal excitability. Ann Neurol. 1996 Oct;40(4):628-34. doi: 10.1002/ana.410400413.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CHUBX2013/08
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.
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