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Individualized rTMS for Motor Recovery in Stroke Patients

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National Taiwan University

Status

Enrolling

Conditions

Stroke
Transcranial Magnetic Stimulation

Treatments

Device: Repetitive transcranial magnetic stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT05914038
202301225DIND

Details and patient eligibility

About

This study aimed to aim to investigate the efficacy of individualized rTMS according to lateralization index on motor recovery and cortical excitability in subacute stroke patients.

Full description

Repetitive transcranial magnetic stimulation (rTMS) is a non-invasive neuromodulation technology.

High and low frequencies of rTMS could modulate the excitability of the cerebral cortex. Theta burst stimulation (TBS) has achieved a similar effect to traditional rTMS mode.

However, the current rTMS studies for stroke patients utilized the same therapeutic protocol and there is no individualized rTMS protocol based on the value of lateralization index.

This study aimed to aim to investigate the efficacy of individualized rTMS according to lateralization index on motor recovery and cortical excitability in subacute stroke patients.

Enrollment

40 estimated patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Unilateral ischemic or hemorrhagic stroke
  2. Stroke within 3 months
  3. Medical Research Council Scale for Muscle Strength in upper limb ≤ 3
  4. No previous stroke, seizure, dementia, Parkinson's disease or other degenerative neurological diseases.
  5. Patient could sit over 15 minutes
  6. Age over 20

Exclusion criteria

  1. Previous stroke, traumatic brain injury, brain tumor
  2. With central nervous system disease (spinal cord injury, Parkinson's disease)
  3. Any contraindication to rTMS (seizure, alcoholism, metal implant, pacemaker)
  4. Patients unable to cooperate the treatment
  5. Pregnancy
  6. Depression

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 2 patient groups

individualized rTMS
Experimental group
Description:
Patients will receive individualized repetitive transcranial magnetic stimulation according to lateralization index measured by functional near-infrared spectroscopy
Treatment:
Device: Repetitive transcranial magnetic stimulation
Traditional rTMS
Active Comparator group
Description:
Control group is given traditional rTMS
Treatment:
Device: Repetitive transcranial magnetic stimulation

Trial contacts and locations

1

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Central trial contact

Yan Ci Liu, PhD; Meng Ting Lin, M.D.

Data sourced from clinicaltrials.gov

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