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Clinical Trials/ISRCTN84827527
ISRCTN84827527
Completed
未知

Aphasia rehabilitation based on mirror neuron theory: a randomized-block-design study of neuropsychology and functional magnetic resonance imaging

the First Affiliated Hospital with Nanjing Medical University0 sites24 target enrollmentJanuary 10, 2019

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
the First Affiliated Hospital with Nanjing Medical University
Enrollment
24
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

2019 Results article in https://www.ncbi.nlm.nih.gov/pubmed/30762012 results

Registry
who.int
Start Date
January 10, 2019
End Date
January 5, 2015
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Stroke patients with aphasia:
  • 1\. First occurrence of cerebral infarction or hemorrhage
  • 2\. Aged 35–70 years
  • 3\. Disease course lasting for 3–24 months
  • 4\. Right\-handed according to the Edinburgh Handedness Inventory
  • 5\. Educated beyond primary school (more than 5 years of education)
  • 6\. Aphasia determined by Western Aphasia Battery (WAB) (aphasia quotient \<93\.8\)
  • 7\. No obvious attention, memory, and visuo\-spatial function disturbances (Non\-language cognitive function assessment scale, 2013 \>70\)
  • 8\. Retaining part of the auditory ability and tolerance of more than 30 minutes to complete the daily training task
  • Healthy participants:

Exclusion Criteria

  • Stroke patients with aphasia:
  • 1\. Frenchay dysarthria assessment shows moderate to severe dysarthria
  • 2\. Serious speech apraxia or oral and maxillofacial apraxia
  • 3\. Anxiety determined by Hamilton Anxiety Scale or depression determined by Hamilton Depression Scale
  • 4\. Obvious dyssomnia or emotional disturbances
  • 5\. Other diseases likely to aggravate patient’s functional status such as cancer, severe heart or lung disease
  • 6\. Refused training or no desire for training
  • 7\. Severe pain, i.e. pain \>8 out of 10 on a visual analog scale (VAS)
  • Healthy participants:
  • 7\. Poor physical condition for any reason

Outcomes

Primary Outcomes

Not specified

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