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Search / Trial NCT06381388

Interaction Between the Brain Hemispheres - Key to Motor Recovery After Stroke

Launched by JORD VINK · Apr 23, 2024

Trial Information

Current as of August 20, 2025

Not yet recruiting

Keywords

Stroke Transcranial Magnetic Stimulation Continuous Theta Burst Stimulation Upper Limb Recovery Tms C Tbs Interhemispheric Inhibition

ClinConnect Summary

This clinical trial is studying how a specific brain stimulation technique, called continuous theta burst stimulation (cTBS), can help improve movement in patients who have had a stroke. After a stroke, many people experience difficulty using their arms, and this study aims to understand if cTBS can restore normal communication between different parts of the brain involved in movement. Researchers will compare the effects of this treatment on 40 stroke patients with upper limb weakness to 40 healthy individuals of similar age.

To be eligible for the study, stroke patients must be at least 18 years old and have had their first stroke within the last 3 to 6 weeks, resulting in weakness in one arm. Healthy participants must also be at least 18 years old and have normal arm function. During the trial, participants will receive the brain stimulation treatment and will be monitored to see how it affects their movement abilities. Importantly, this trial is not yet recruiting participants, and safety measures are in place to exclude those with certain medical conditions or risks.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria for patients:
  • Age ≥ 18 years;
  • First-ever ischemic stroke or intracerebral hemorrhage in a cerebral hemisphere or the brainstem;
  • Unilateral paresis of an upper extremity with a Motricity Index (MI) between 9 and 99
  • Inclusion possible between 3 weeks and 6 weeks after stroke onset;
  • Signed informed consent.
  • Inclusion Criteria for healthy controls:
  • Age ≥ 18 years;
  • Signed informed consent.
  • Normal motor function with a minimum Motricity Index (MI) of 99.
  • Exclusion Criteria:
  • Disabling medical conditions (severe heart disease, severe head trauma, severe mental illness);
  • Severe deficits in communication, memory or understanding which could impede participation, as determined by the treating physician;
  • Contraindications to TMS and/or MRI (ferrous implants, history of epilepsy, drug or alcohol abuse over a period of 6 months prior to the experiment, pregnancy);
  • Life expectancy shorter than one year;
  • Upper limb paresis prior to stroke onset.

About Jord Vink

Jord Vink is a dedicated clinical trial sponsor committed to advancing medical research and improving patient outcomes through innovative studies. With a focus on collaboration and ethical practices, Jord Vink partners with leading healthcare institutions and researchers to design and implement rigorous clinical trials across various therapeutic areas. Their mission is to generate high-quality data that supports the development of effective therapies, while ensuring the safety and well-being of participants. By leveraging cutting-edge methodologies and fostering a culture of transparency, Jord Vink aims to contribute significantly to the evolving landscape of healthcare and therapeutic advancements.

Locations

Utrecht, , Netherlands

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported