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Acupuncture and magnetic stimulation to help movement after stroke

Tests electrical acupuncture with magnetic brain stimulation in adults recovering from stroke.

Plain-language title generated from the registry record
Registry title: Electroacupuncture and rTMS for Post-Stroke Motor Recovery

Key facts

Where
Fuzhou and Wenzhou, ChinaSee the 3 sites

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 40 and 75 years old?

Source: NCT07113990, who can take part

Where in China

  • Fujian Provincial People's HospitalFuzhou, ChinaNot yet recruiting
  • Fuzhou University Affiliated Provincial HospitalFuzhou, ChinaTaking people
  • Wenzhou Hospital of Traditional Chinese MedicineWenzhou, ChinaNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Jing Tao
Trial code
NCT07113990
Record updated
3 November 2026
Original description
This study aims to evaluate the combined efficacy of repetitive Transcranial Magnetic Stimulation (rTMS) and Electroacupuncture (EA) in improving motor function recovery post-stroke, compared to rTMS combined with sham EA. Participants will receive either active EA or sham EA alongside standard rTMS treatment. Outcomes will be assessed using standardized clinical scales and neuroimaging techniques to explore underlying neuroplasticity mechanisms.Read full original descriptionShow less

Efficacy and Safety of Electroacupuncture Combined With rTMS on Motor Function Recovery After Stroke: A Multi-center Randomized Controlled Clinical Study

This study aims to evaluate the combined efficacy of repetitive Transcranial Magnetic Stimulation (rTMS) and Electroacupuncture (EA) in improving motor function recovery post-stroke, compared to rTMS combined with sham EA. Participants will receive either active EA or sham EA alongside standard rTMS treatment. Outcomes will be assessed using standardized clinical scales and neuroimaging techniques to explore underlying neuroplasticity mechanisms.

Inclusion: 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: Presence of metallic implants or contraindications for MRI; Pregnancy, breastfeeding, or concurrent participation in other clinical trials affecting outcomes; History of epilepsy or familial epilepsy; Severe aphasia or cognitive impairment (MoCA < 18); Severe systemic complications (e.g., severe organ dysfunction, deep vein thrombosis); Motor dysfunction due to non-vascular causes (e.g., tumor, trauma); Severe anxiety (HAMA > 7) or depression (HAMD > 8); Severe spasticity (modified Ashworth ≥ 2); Fear or intolerance of TMS or electroacupuncture.

ClinicalTrials.gov NCT07113990