Actively Recruiting

Phase Not Applicable
Age: 30Years - 80Years
All Genders
ID07570212

Exploration of the Efficacy of Individualized Transcranial Magnetic Stimulation in the Treatment of Parkinsonian Disorders

Led by Peking University First Hospital · Updated on 2026-05-06

50

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

Sponsors

P

Peking University First Hospital

Lead Sponsor

C

Changping Laboratory

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating whether individualized targeted repetitive transcranial magnetic stimulation (rTMS) can improve both motor and non-motor symptoms in patients with parkinsonian disorders, including Parkinson's Disease, Multiple System Atrophy, and Progressive Supranuclear Palsy. The study aims to determine if this treatment alleviates symptoms and which clinical features respond best to the therapy. Participants will receive a 10-day rTMS treatment over two weeks, with sessions held once daily from Monday to Friday. The stimulation uses intermittent theta burst stimulation (iTBS) targeting specific brain areas with a figure-of-eight coil in the left hemisphere. Each day involves multiple stimulation trains totaling 14,400 pulses. Before treatment, participants undergo screening with clinical assessments, MRI, and EEG. Follow-up assessments occur immediately after treatment and again 10 weeks later. During the study, participants will have clinical tests, MRI scans, and EEG recordings to evaluate changes in motor function, mobility, and non-motor symptoms. Researchers will measure outcomes such as motor symptom changes using the MDS-UPDRS Part III scale, mobility with the 5-meter Timed Up and Go test, and non-motor symptoms via a questionnaire. Safety and treatment effects will be monitored throughout the study period lasting approximately 12 weeks from screening to final follow-up.

CONDITIONS

Brief Title

Individualized Transcranial Magnetic Stimulation in Parkinsonian Disorders

Who Can Participate

Age: 30Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinically established or probable diagnosis of Parkinson's Disease, Multiple System Atrophy, or Progressive Supranuclear Palsy according to MDS criteria
  • Age between 30 and 80 years, inclusive
  • PD patients with Modified Hoehn and Yahr stage 2-4
  • MSA patients with UMSARS Part IV stage 1-4
  • PSP patients with Modified Rankin Scale grade 2-4
  • Ability to understand and comply with study requirements and provide written informed consent
Not Eligible

You will not qualify if you...

  • Presence of intracranial metallic implants or foreign bodies such as cochlear implants or pacemakers
  • Known allergy to EEG conductive paste or contraindications to EEG
  • History of claustrophobia, incompatible implants, or extensive tattoos preventing MRI
  • Currently receiving TMS or other physical therapies like tDCS
  • Unstable systemic diseases needing urgent treatment
  • Personal or family history of epilepsy
  • History of moderate-to-severe psychiatric disorders
  • Chronic insomnia or regular use of sedative-hypnotics
  • Current use of medications that significantly affect central nervous system excitability

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 10 consecutive working days

Participants receive individualized transcranial magnetic stimulation (iTBS) sessions targeting the left hemisphere's somato-cognitive action network sites over ten consecutive working days.

Daily visits for 10 days with multiple stimulation sessions per day

Follow-up

Duration - 10 weeks

Participants are monitored for changes in motor and non-motor symptoms up to 10 weeks after treatment.

1 to 2 visits depending on assessments

Trial Site Locations

Total: 1 location

1

Peking University First Hospital

Beijing, Beijing Municipality, China, 100034

Actively Recruiting

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Research Team

L

Luhua Wei, M.D.

K

Kai Li, M.D.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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