Ignite Creation Date:
2024-05-06 @ 8:15 PM
Last Modification Date:
2024-10-26 @ 3:24 PM
Study NCT ID:
NCT06316557
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-03-18
First Post:
2024-03-12
Brief Title:
High-frequency rTMS on the Cerebellar to Improve Post-stroke Cognitive Impairment
Sponsor:
Beijing Tiantan Hospital
Organization:
Beijing Tiantan Hospital
Study Overview
Official Title:
High-frequency Repetitive Transcranial Magnetic Stimulation on the Cerebellar Hemisphere to Improve Post-stroke Cognitive Impairment
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
HOPE
Brief Summary:
The objective of this clinical trial is to investigate the effectiveness and safety of repetitive transcranial magnetic stimulation rTMS in the cerebellum for individuals with post-stroke cognitive impairment Participants will undergo rTMS in the cerebellar hemisphere opposite the lesion site once daily for a total of five days
Detailed Description:
The primary objective of this clinical trial is to investigate the effectiveness and safety of high-frequency repetitive transcranial magnetic stimulation rTMS in the cerebellum for individuals with post-stroke cognitive impairment The trial aims to answer two main questions 1 What is the effectiveness of high-frequency rTMS in improving post-stroke cognitive impairment 2 Is high-frequency rTMS in the cerebellum safe for individuals with post-stroke cognitive impairment Participants will undergo 5Hz rTMS in the cerebellar opposite the lesion site once daily for a total of five days The control group will receive sham rTMS with the same parameters and positions By comparing the effectiveness of rTMS for post-stroke cognitive impairment between the two groups researchers will assess the potential benefits of rTMS
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None