Actively Recruiting
High-Frequency Repetitive Transcranial Magnetic Stimulation for Cognitive Improvement in Patients With Post-Stroke Cognitive Impairment
Led by Qilu Hospital of Shandong University · Updated on 2026-04-23
40
Participants Needed
1
Research Sites
65 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To clarify the clinical efficacy of high-frequency rTMS on patients with post-stroke cognitive impairment, fNIRS and EEG techniques were used to observe the changes in brain functional activities of patients with post-stroke cognitive impairment after rTMS treatment, and to clarify the neuroregulatory effect of rTMS on patients with post-stroke cognitive impairment.
CONDITIONS
Official Title
High-Frequency Repetitive Transcranial Magnetic Stimulation for Cognitive Improvement in Patients With Post-Stroke Cognitive Impairment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with stroke confirmed by cranial CT or MRI as initial onset
- Stroke occurred within 1 to 12 months
- Cognitive impairment with MoCA score below 26 (adjusted for education)
- Aged between 35 and 75 years
- Stable vital signs with no worsening neurological symptoms
- No severe speech, vision, or hearing problems; able to complete the study
- Not currently using antidepressant drugs
- If using cognitive-enhancing drugs, must have used for at least 3 weeks without dose changes
- Voluntary participation with signed informed consent
You will not qualify if you...
- History of brain tumors, brain trauma, epilepsy, or mental disorders
- Cognitive impairment present before the stroke
- Previous craniotomy or skull defects
- Implanted metal or electronic devices such as pacemakers or cochlear implants
- Other serious illnesses that could affect the study
- Pregnant women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Qilu Hospital of Shandong University
Jinan, China
Actively Recruiting
Research Team
R
RUN SHENG
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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