Actively Recruiting

Phase Not Applicable
Age: 50Years +
All Genders
NCT06350617

Personalized rTMS Protocol Based on Functional Reserve to Enhance Ambulatory Function in PD Patients

Led by Samsung Medical Center · Updated on 2026-04-28

60

Participants Needed

1

Research Sites

136 weeks

Total Duration

On this page

Sponsors

S

Samsung Medical Center

Lead Sponsor

N

National Research Foundation of Korea

Collaborating Sponsor

AI-Summary

What this Trial Is About

The objective of this study was to determine the effects of protocols of repetitive transcranial magnetic stimulation (rTMS) therapy based on the functional reserve of each patient with Parkinson's disease, compared to conventional high-frequency rTMS therapy on bilateral primary motor cortex (M1). Investigators hypothesized that the functional reserve of each patient with Parkinson's disease will be different, and therefore an appropriate simulating target for rTMS therapy is needed. In addition, this approach could be more effective compared to conventional protocols applied to patient with Parkinson's disease regardless of their severity, predicted mechanism of motor function recovery, or functional reserves.

CONDITIONS

Official Title

Personalized rTMS Protocol Based on Functional Reserve to Enhance Ambulatory Function in PD Patients

Who Can Participate

Age: 50Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with Parkinson's disease by UK Parkinson's Disease Society Brain Bank criteria
  • Modified Hoehn and Yahr stage between 2 and 4
  • Able to walk on flat surfaces without a gait aid
  • Aged 50 years or older
  • Willing to sign informed consent
Not Eligible

You will not qualify if you...

  • Contraindications to rTMS such as epilepsy, metal implants in the head, or history of craniotomy
  • Cognitive impairment based on Montreal Cognitive Assessment (MoCA) below educational thresholds
  • Other neurological conditions like spinal cord injury or stroke
  • Major psychiatric disorders including major depression, schizophrenia, or dementia
  • Severe on-off phenomena or dyskinesia making study participation unsuitable
  • Contraindications to MRI
  • Pregnant or lactating
  • Refusal to participate in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Samsung Medical Center

Seoul, South Korea, 06351

Actively Recruiting

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Research Team

W

Won Hyuk Chang, PhD

CONTACT

H

Ho Seok Lee, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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