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Impact of Intermittent Theta Burst Stimulation on Oscillatory Brain Activity in Patients with Post-stroke Cognitive Impairment: A Resting-State EEG Study

Impact of Intermittent Theta Burst Stimulation on Oscillatory Brain Activity in Patients with Post-stroke Cognitive Impairment: A Resting-State EEG Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103236
Enrollment
Unknown
Registered
2025-05-27
Start date
2024-07-01
Completion date
Unknown
Last updated
2025-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-stroke cognitive impairment

Interventions

Pre-iTBS :iTBS stimulates the left dorsolateral prefrontal lobe.
Sham stimulus control group:Sham stimulation was performed in the control group.

Sponsors

Zhongshan City People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Clear diagnosis of ischemic stroke, and all of them have been confirmed by brain MRI scan as a single lesion; 2. First stroke, and in the subacute stage (within 6 weeks of onset); 3. Right hand; 4. Age 18-80 years old; 5. Stable condition with no progressive neurological symptoms; 6. Informed and willing to participate in this clinical study; 7. Able to cooperate in the completion of all neuropsychological tests and EEG recordings.

Exclusion criteria

Exclusion criteria: 1. Multi-site or large-area ischemic stroke confirmed by cranial MR; 2. There are contraindications to TMS treatment, such as metal implants, pacemakers or skull defects in the body; 3. Have a history or risk of seizures or have taken anti-epileptic drugs; 4. Previous neuroorganic lesions of the brain, such as brain tumor or traumatic brain injury, and history of brain surgery; 5. The patient has serious diseases of important organs such as heart, liver, kidney or other serious physical diseases; 6. The patient has a history of organic psychosis or affective psychosis or related diseases, such as schizophrenia or depression; 7. Those who cannot complete neuropsychological tests and EEG recordings; 8. Long-term history of alcoholism, severe alcohol abuse and drug abuse; 9. Pregnant women; 10. Refusal to participate in this clinical study.

Design outcomes

Primary

MeasureTime frame
Absolute power;

Secondary

MeasureTime frame
Relative Power;Inter-band Power Ratio;Brain Symmetry Power Ratio;

Countries

China

Contacts

Public ContactXu Ruikai

Zhongshan City People’s Hospital

xurk3@mail2.sysu.edu.cn+86 156 2220 4779

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026