wearable rTMS
DeviceApplication of inhibitory low-frequency rTMS on unaffected primary motor cortex by wearable rTMS
NCT Number: NCT06543797
To explore the safety of applying repetitive low-frequency transcranial magnetic stimulation using a wearable medical electromagnetic generator in stroke patients.
Trial opening soon.
Get Notified19 year–80 year
All sexes
Interventional
Early Phase 1
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Application of inhibitory low-frequency rTMS on unaffected primary motor cortex by wearable rTMS
Time frame: Before and after 2 weeks of intervention / Soon after every intervention
All types of adverse events that occurred during clinical trials
Time frame: Before and after 2 weeks of intervention
Fugl-Meyer assessment for motor function in score
Time frame: Before and after 2 weeks of intervention
Manual muscle test for strength in score
Time frame: Before and after 2 weeks of intervention
Box and block test for gross manual dexterity in number of blocks from on compartment of a box to another of equal size within 60 seconds
Time frame: Before and after 2 weeks of intervention
Action research arm test for functional ability of upper extremity in score
Time frame: Before and after 2 weeks of intervention
Korean mini mental state exam for cognitive function in score
Time frame: Before and after 2 weeks of intervention
Korean version of modified barthel index for functional status in score
Time frame: Before and after 2 weeks of intervention
Geriatric depression scale for depression in scale
Time frame: Before and after 2 weeks of intervention
Electroenchphalography is a test that measures EEG power in alpha band
Time frame: Before and after 2 weeks of intervention
Evoked potential is an electrical potential recorded from the nervous system of a human or animal following presentation of a stimulus. In this study, motor- and sensory- evoked potentials are included.
Time frame: Before and after 2 weeks of intervention
Motion analysis with motion capture setup and data processing or streaming of patients movements. In this study, data of motion capture include kinetic and kinematic data including physiological parameter.
Time frame: Before and after 2 weeks of intervention
Funtional near-infrared spectroscopy meausures cortical activity in concentration of oxy- and deoxy-hemoglobin
Time frame: Before and after 2 weeks of intervention
Blood biomarker include expression of tumor necrosis factor (TNF)-a and interleukin (IL)-1b
Contact information is provided by the study sponsor or research team.
Bundang CHA Hospital
Other
A Prospective, Single-center, Single-group, Investigator-led Exploratory Clinical Trial to Determine the Safety of the Application of a Wearable Medical Electromagnetic Generator.
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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