Electroacupuncture and rTMS for Post-Stroke Motor Recovery
Launched by JING TAO · Aug 3, 2025
Trial Information
Current as of August 19, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a new way to help people recover movement after a stroke. It looks at whether combining two treatments—repetitive Transcranial Magnetic Stimulation (rTMS), which uses magnetic pulses to stimulate the brain, and Electroacupuncture (EA), which involves gentle electrical stimulation through acupuncture needles—can improve motor function better than rTMS with a fake (sham) version of electroacupuncture.
People who might join this study are adults aged 40 to 75 who have had their first stroke affecting one side of the brain and causing movement problems. Their stroke should have happened between two weeks and six months ago, and they need to be right-handed and able to follow instructions. Participants will receive either real or sham electroacupuncture along with rTMS and will be monitored using tests and brain scans to see how well they recover and how their brains change. The study is not yet recruiting, and certain conditions like epilepsy, severe mental health issues, or other medical problems might exclude someone from joining.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Diagnosed with stroke confirmed by neuroimaging (CT/MRI).
- • First-ever stroke, unilateral hemispheric lesion, related to motor dysfunction.
- • Age between 40 and 75 years.
- • Duration from stroke onset between 2 weeks and 6 months.
- • Brunnstrom stage II-IV.
- • Right-handed.
- • Able to understand instructions and voluntarily provide written informed consent.
- Exclusion Criteria:
- • History of epilepsy or familial epilepsy.
- • Motor dysfunction due to non-vascular causes (e.g., tumor, trauma).
- • Severe aphasia or cognitive impairment (MoCA \< 18).
- • Severe systemic complications (e.g., severe organ dysfunction, deep vein thrombosis).
- • Presence of metallic implants or contraindications for MRI.
- • Severe anxiety (HAMA \> 7) or depression (HAMD \> 8).
- • Severe spasticity (modified Ashworth ≥ 2).
- • Fear or intolerance of TMS or electroacupuncture.
- • Pregnancy, breastfeeding, or concurrent participation in other clinical trials affecting outcomes.
About Jing Tao
Jing Tao is a dedicated clinical trial sponsor committed to advancing medical research and enhancing patient care through innovative therapeutic solutions. With a focus on developing groundbreaking treatments across various therapeutic areas, Jing Tao leverages cutting-edge technology and a robust network of clinical professionals to conduct rigorous trials that meet the highest ethical and regulatory standards. Their mission is to streamline the drug development process while prioritizing patient safety and efficacy, ultimately contributing to improved health outcomes and quality of life for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Wenzhou, Zhejiang, China
Fuzhou, Fujian, China
Fuzhou, Fujian, China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported