Predicting Language Recovery in Acute Stroke Patients in the Neurovascular Intensive Care Unit: An Exploratory Study With the Core Assessment of Language Processing.

Обзор

Introduction: Stroke affects one person every 4 minutes in France (i.e. more than 140,000 new cases per year) resulting in cognitive and motor disorders. Aphasia is one of the most devastating cognitive disorders that persist in the late phase. However, early treatment of aphasia can improve the effects of rehabilitation. Identifying, as early as possible, the patients most at risk of presenting persistent language disorders in the late phase would make it possible to improve their management and increase the effects of cognitive rehabilitation on their language abilities. The aim of this project is to evaluate whether the Core Assessment of Language Processing (CALAP) assessed in the acute phase of stroke can predict language abilities in the late phase. Hypothesis/Objective: The primary objective is to determine whether the language abilities of patients in the acute phase of stroke can be used to predict language abilities in the late phase. Secondary objectives are to determine whether prediction can be improved with (1) brain MRI data and (2) neuropsychological assessment data. The (3) secondary objective is to determine whether cognitive abilities at the chronic phase can be predicted by language performance in the acute phase. The (4) secondary objective is to assess whether language rehabilitation modifies the predictive power of the language abilities assessed with the CALAP. Method: Patients will be included during their hospitalization after a brain vascular injury (acute phase, up to 21 days of hospitalization). After discharge, they will return for a post-stroke assessment between 3 and 18 months after the acute phase. During these two visits, a clinical and neurological examination, a neuropsychological assessment and an MRI will be performed. A prediction model (development and validation) will be used for all objectives using a linear regression model with cross validation. The entire sample consists of stroke patients. The study is single-center and will have a total duration of 6 years with an estimated 570 patients included. Conclusion: Predicting the language abilities of a post-stroke patient will improve clinical management and direct patients requiring language rehabilitation to appropriate care.

Вмешательства

• Другое Data recovery from language and cognitive assessment
  Data recovery from language assessment: Core Assessment of LAnaguage Processing, and from neuropsychological assessment : Montreal Cognitive Assessment, Trail Making Test, Batterie Rapide d'Efficience Frontale (BREF), animal fluency, 5 words of Dubois, Ne

Первичные конечные точки

• Language recovery prediction with Core Assessment of Language Processing score [Срок оценки: 18 months after stroke]

Вторичные конечные точки (4)

• Improving CALAP recovery prediction using MRI data [Срок оценки: 18 months after stroke]
• Improving CALAP recovery prediction using neuropsychological data [Срок оценки: 18 months after stroke]
• Cognitive recovery prediction with Core Assessment of Language Processing score [Срок оценки: 18 months after stroke]
• Improving CALAP recovery prediction using language rehabilitation data [Срок оценки: 18 months after stroke]

Критерии участия

Критерии включения

• Age: between 18 and 85 years old
• Inpatient in the initial phase of stroke (between 0 and 21 days after stroke)
• Hemispheric stroke, ischemic or haemorrhagic
• Ability to participate in tests
• Francophone
• 4≤ NIHSS score ≤21 or if NIHSS score < 4, LAST score \[0-13\]
• Non-opposition to participation in tests

Критерии исключения

• Severe alertness impairment incompatible with test participation, NIHSS score 1a. different from 0
• Severe overall intellectual deterioration incompatible with test participation
• Patients who may have a visual or hearing impairment incompatible with participation in CALAP
• History of stroke
• Posterior fossa stroke

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения

Когортное

Центры проведения

Франция · 1 центр

• Assistance Publique Hôpitaux de Paris - Hôpital Henri Mondor — Créteil

Идентификаторы

NCT: NCT06817642 · APHP220542

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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