Using magnetic stimulation to improve arm function after stroke

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial evaluates the safety and effectiveness of repetitive transcranial magnetic stimulation (rTMS) to enhance upper extremity function in patients who have experienced a stroke. It employs a randomized, controlled, and blind methodology, utilizing functional magnetic resonance imaging (fMRI) to identify specific brain regions for targeted stimulation. The study focuses on individuals who are at least three months post-stroke, a period often associated with slow recovery. By combining rTMS with fMRI insights, the trial aims to establish a more effective rehabilitation approach for stroke survivors.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adults over 20 years of age
* Patients 3 months or more after stroke onset
* Patients with NIHSS score of 1 or more to 20 or less
* After hearing and fully understanding the detailed explanation of this clinical trial, the subject or legal representative voluntarily decides to participate and agrees in writing to abide by the precautions

Exclusion Criteria: Patients who fall under one or more of the following conditions are not eligible to participate in the study.

* Patients with systemic infectious disease at the time of participation in the clinical trial
* In the case of a person with impaired consent (MMSE less than 10 points), if not accompanied by a guardian
* Those with severe medical conditions such as unstable conditions of the cardiovascular system, digestive system, respiratory system, endocrine system, etc., who are in poor general condition
* Other cases where the researcher determines that participation in this clinical trial is not appropriate
* Those who are contraindicated in repetitive transcranial magnetic stimulation A. When metal materials (deep brain stimulation electrode, brain aneurysm clip, cardiac pacemaker, etc.) are in the body B. Uncontrolled epilepsy (epilepsy), patients with psychiatric disorders
* Pregnant, lactating women and patients with potential for pregnancy
* Patients with contraindications for imaging tests
* Those who have undergone cerebral surgery due to past or current related medical history

Where it's running

• Department of Rehabilitation Medicine, CHA Bundang Medical Center
  Seongnam, Korea, Republic of Recruiting

Study contacts

• Principal investigator: Kim MinYoung, M.D., Ph.D. — CHA University
• Study coordinator: Kim MinYoung, M.D., Ph.D.
• Email: kmin@cha.ac.kr
• Phone: 82-31-780-6281

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• AI-based tools to help diagnose, treat and predict stroke outcomes across multiple hospitals

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• Web-based therapy using action observation and mirror therapy for arm weakness after stroke

  This trial tests whether a mobile telerehabilitation app delivering action observation therapy (AOT) alone or combined AOT with mirror therapy (AOT-MT) can improve upper limb function in people with subacute stroke.

  Recruiting Chang Gung Memorial Hospital · Taoyuan · NCT07921108

• Remote Ischaemic Conditioning for Fatigue After Stroke 2

  Aat least 12 weeks after stroke, adults with post-stroke fatigue will try a simple hand-arm cuff treatment at home to see if it helps reduce fatigue.

  Recruiting Phase 2 Sheffield Teaching Hospitals NHS Foundation Trust · Sheffield, South Yorkshire · NCT07914647

• Dual-task balance training plus computer-based cognitive training after stroke

  In adults who recently had a stroke, the study tests whether adding computerized cognitive exercises to balance training improves balance and other recovery outcomes.

  Recruiting Matia Foundation · San Sebastián, GUIPUZCOA · NCT07913620

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.