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Clinical Trial Summary

The purpose of this study is to form an interdisciplinary team to dynamically evaluate patient cognitive outcomes and develop an individualized cognitive training program for Chinese brain tumor patients


Clinical Trial Description

Adult patients diagnosed with glioma who meet the inclusion criteria will be enrolled in this study. Patients admitted to Neurosurgery Ward 1 and Ward 2 will be assigned to the intervention group, while those admitted to Neurosurgery Ward 3 and Ward 4 will serve as the control group. The intervention group will receive cognitive rehabilitation training based on the Remind strategy in addition to standard rehabilitation care, whereas the control group will receive only standard rehabilitation care. Assessment of patients' cognitive function, quality of life, psychological status, and the effectiveness of cognitive training intervention will be conducted on the first day of admission, one day before discharge, and at the end of the intervention period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06327048
Study type Interventional
Source LanZhou University
Contact yuanyuan ma, Bachelor
Phone 0931-18809406184
Email 1657107645@qq.com
Status Recruiting
Phase N/A
Start date March 6, 2024
Completion date December 1, 2024

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