Stroke Clinical Trials

Find Stroke Clinical Trials Near You

Efficacy of High-Frequency Repetitive Transcranial Magnetic Stimulation in Patients With Post-Stroke Cognitive Impairment: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Device, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 35
Maximum Age: 75
Healthy Volunteers: f
View:

• Meets the diagnostic criteria for stroke as stipulated in the Guidelines for the Prevention and Treatment of Stroke in China (2021 Edition), and the initial stroke diagnosis is confirmed by cranial CT or MRI examination, and is confirmed as the initial onset;

• The disease course is 1-12 months;

• Has cognitive impairment (MoCA \< 26 points, education years ≤ 12 years, add 1 point to the score result);

• Age 35-75 years old, gender not limited;

• Stable vital signs, no progressive neurological symptoms;

• No severe aphasia, visual or auditory impairment, and able to complete the research protocol;

• Not using antidepressant drugs simultaneously;

• If using cognitive-improving drugs (such as donepezil, memantine), it should last for at least 3 weeks or more, and no dose adjustment will be made during the enrollment period;

• Voluntarily participate and sign the informed consent form.

Locations
Other Locations
China
Qilu Hospital of Shandong University
RECRUITING
Jinan
Contact Information
Primary
RUN SHENG
shengrun2001@163.com
8615069169127
Time Frame
Start Date: 2026-04-01
Estimated Completion Date: 2027-07-01
Participants
Target number of participants: 40
Treatments
Sham_comparator: the control group
The control group will undergo rTMS sham stimulation therapy combined with conventional rehabilitation treatment, using a sham stimulation coil.
Experimental: The rTMS stimulation group
The experimental group will receive rTMS stimulation therapy, which involves applying high-frequency 10Hz rTMS to the patients' heads for 20 minutes, followed by conventional rehabilitation treatment.
Related Therapeutic Areas
Sponsors
Leads: Qilu Hospital of Shandong University

This content was sourced from clinicaltrials.gov