Communication Book in Pragmatic Communication in Vascular Aphasics
NCT ID: NCT04070625
Last Updated: 2019-08-28
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
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COMPLETED
34 participants
OBSERVATIONAL
2009-02-17
2012-02-10
Brief Summary
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Detailed Description
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This study aims to evaluate, in communication tasks, the pragmatic effectiveness of the communication book in the general conditions of use and its maintenance in the implementation of the compensatory strategies of communication in severe aphasias.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Communication book group
Speech therapy with communication book
Communication book group
Communication book
Control group
Simple speech therapy
Control group
Simple speech therapy
Interventions
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Communication book group
Communication book
Control group
Simple speech therapy
Eligibility Criteria
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Inclusion Criteria
* aphasic subjects admitted to hospital or seen in consultation following a 1st ischemic or hemorrhagic symptomatic vascular accident constituted
* during the first year of onset of aphasia
* adults over 18 years old
* French
* phasic disorder of severe severity expression (overall severity score between 0 and 2 at the diagnostic battery for the assessment of aphasia scale)
* residual ability to understand clinical assessments and informed consent; information about the objectives and the procedure of the research will also be given to the patient's designated confidant
* motor capacity for comfortable sitting and transfers with help
* affiliation to health insurance
* no deficits in visual perceptual tests (researched using the visual decision of objects and Montreal protocol for the evaluation of visual gnosis), which allows the use of the communication book,
Exclusion Criteria
* disturbance of vigilance
* insane state
* psychiatric history requiring hospitalization in a specialized environment
* perceptual disturbance, visual agnosia not allowing the use of the image support
* pregnancy or breastfeeding
* administration after the occurrence of stroke of a product for which an effect on the recovery of aphasia has been reported: piracetam, bromocriptine, donepezil, dextroamphetamine (if treatment with these products has been performed, inclusion is possible after a weaning period of 15 days)
* simultaneous inclusion in another therapeutic protocol of language disorders
18 Years
ALL
No
Sponsors
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University Hospital, Bordeaux
OTHER
Responsible Party
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Principal Investigators
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Pierre-Alain JOSEPH, Pr
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Bordeaux
Other Identifiers
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CHUBX 2008/10
Identifier Type: -
Identifier Source: org_study_id
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