Ischemic Stroke Clinical Trial
Official title:
The Language Functional Reorganization Following Subcortical Cerebral Infarction: A Longitudinal fMRI Study
Verified date | October 2018 |
Source | Guangzhou General Hospital of Guangzhou Military Command |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Post stroke aphasia (PSA) is one of the most frequently happened deficiency of stoke,
affecting speaking,comprehension, writing and reading of language. Generally, PSA is commonly
seen in cortical damage, but in recent years it has been found that subcortical injury is
also an important cause of PSA, which is called subcortical aphasia. Using fMRI technology,
the investigators aim to investigate the language function of patients with subcortical
cerebral infarction at different stages of recovery , and explored the mechanism of
post-injury language reorganization in the brain.
The investigators recruited 60 first-episode acute cerebral infarction patients with one-side
lesion in subcortical white matter (40 with left injury and 20with right injury) and 20
health volunteers. All participants are right-handed, and screened with MMSE, HAMD and HAMA
to exclude cases of psychosis, post-stroke dementia and depression. Each participant was
arranged to have three test sessions at different stages after the infarction (T1:within 3
days after onset of the stroke ; T2:28 ±3days after onset; T3: 90±3days after onset), with
fMRI and Western aphasia battery (WAB) in each session.
The purpose of this study is to explore the pathogenesis of subcortical aphasia, and to
understand the dynamic reorganization of language network during the recovery of language
function.
Status | Completed |
Enrollment | 80 |
Est. completion date | January 12, 2017 |
Est. primary completion date | October 9, 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - The first stroke of the left single subcortical areas, within 72hours. - Primary school or higher level,aged between 18-75, native language Chinese - According to the commonly used eye chart examination, the corrected visual acuity is more than 1.0. - According to the Edinburgh Handedness Questionnaire (EHQ) as the right handed. - The language function was normal before the onset. After the onset, the language function was mildly to moderately impaired with Western Aphasia Battery (WAB) ( Aphasia Quotient (AQ) between in 60 to 88). - The patient cooperate with the examination, they and their guardian signed the informed consent Exclusion Criteria: - History of organic diseases of the nervous system and history of craniocerebral trauma. - History of epilepsy and psychosis. - History of material dependence. - Decompensation of important organ function. - Hamilton Depression Scale(HAMD )>8 points. - Hamilton Anxiety Scale(HAMA )>7 points. - The Mini-Mental State Examination (MMSE)score <20 points. - Pregnant women and breast-feeding women. - Contraindication of MRI scanning. |
Country | Name | City | State |
---|---|---|---|
China | Cerebrovascular Department of General Hospital of Guangzhou Military Command of PLA | GuangZhou | Guangdong |
Lead Sponsor | Collaborator |
---|---|
Guangzhou General Hospital of Guangzhou Military Command |
China,
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* Note: There are 63 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | A change of outcome measure: the Chinese version of Western Aphasia Battery(WAB) | The main outcome measure for this scale is Aphasia Quotient(AQ) which mainly tests the ability of spontaneous speech, oral comprehension, repetition, and naming, and reflects the severity of aphasia, and can be used as a reliable indicator to evaluate the improvement and deterioration of aphasia. Score fluctuation is 0-100 points, the normal value is 98.4-100 points, AQ<93.8 can be judged as language dysfunction. | This is an outcome measure to assess the improvement of language function from onset to 3 months after treatment. Thus, participates will undergo this assessment within 3 days (V1), 28±3 days (V2), and 90±3 days(V3) after randomization. | |
Secondary | A change of outcome measure: Spontaneous Language Frequency Test(SLFT) | This test mainly assesses spontaneous speech fluency of participants. It requires participants name as many food names as possible within one minute, and each correct one to give one point. The higher the score, the better the language function. | This is an outcome measure to assess the improvement of language function from onset to 3 months after treatment. Thus, participates will undergo this assessment within 3 days (V1), 28±3 days (V2), and 90±3 days(V3) after randomization. | |
Secondary | A change of outcome measure: Picture Naming Test(PNT) | This test mainly assesses the ability of picture name of participants. we used a program for displaying named pictures on a computer screen (60 photos in total, of which 20 were Chinese celebrity faces). Each image was displayed in 3 seconds, and 1 point was correctly named for an image. The faces of celebrities were selected from the picture database of Chinese celebrities in the State Key Laboratory of Cognitive Neuroscience and Learning at Beijing Normal University. Score fluctuation is 0-60 points, the higher the score, the better the ability of picture name. | This is an outcome measure to assess the improvement of language function from onset to 3 months after treatment. Thus, participates will undergo this assessment on the within 3 days (V1), 28±3 days (V2), and 90±3 days(V3) after randomization. | |
Secondary | Follow-up measurement:Functional Magnetic Resonance Imaging(fMRI) | The examine included task-state fMRI and resting-state fMRI Time Frame: We will explore the mechanisms of dynamic changes in language functions. Thus, participates will undergo this examine on the first days (V1), 28±3 days (V2), and 90±3 days (V3) after randomization.. | This is an outcome measure to assess the improvement of language function from onset to 3 months after treatment. Thus, participates will undergo this assessment within 3 days (V1), 28±3 days (V2), and 90±3 days(V3) after randomization. |
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