Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
All Genders
NCT07309198

Temporal Interference Stimulation on Motor Symptoms in Parkinson's Disease

Led by Shanghai University of Sport · Updated on 2026-01-06

36

Participants Needed

1

Research Sites

22 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn whether a type of brain stimulation called transcranial temporal interference stimulation (TIS) of the internal globus pallidus (GPi) can help improve movement symptoms in people with Parkinson's disease. The study will also look at how TIS changes brain activity related to these improvements. The main questions this study aims to answer are: * How much can repeated TIS sessions improve movement symptoms in people with Parkinson's disease? * Can these improvements last for up to two months after the treatment ends? * What changes in brain activity happen along with the improvements? Researchers will compare people who receive active TIS with those who receive sham (placebo-like) stimulation to see whether active TIS leads to better movement outcomes. Participants will: * Receive 10 sessions of active or sham TIS over two weeks * Complete movement assessments during the two-week treatment and again 2, 4, and 8 weeks afterward * Complete brain activity assessments before and after the two-week treatment

CONDITIONS

Official Title

Temporal Interference Stimulation on Motor Symptoms in Parkinson's Disease

Who Can Participate

Age: 50Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with idiopathic Parkinson's disease by a physician using MDS criteria, with disease onset after age 40
  • Stable Parkinson's medication, including levodopa, unchanged for at least 4 weeks before and during the study
  • Hoehn and Yahr stage between 1.5 and 3
  • Able to walk without help
  • Montreal Cognitive Assessment score of 21 or higher indicating no dementia
  • Aged between 50 and 80 years
Not Eligible

You will not qualify if you...

  • Any contraindications for MRI or TIS, such as claustrophobia, metal implants in head or heart, or past electroconvulsive therapy
  • Currently taking antipsychotic, antidepressant, or other dopamine-modulating drugs
  • Orthopedic issues that affect movement tests, including osteoarthritis or recent surgery within 6 months
  • History of major psychiatric illness diagnosed by a physician
  • Cardiovascular risks that prevent exercise or study participation
  • Previous deep brain stimulation surgery

AI-Screening

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Trial Site Locations

Total: 1 location

1

Shanghai University of Sport

Shanghai, Shanghai Municipality, China, 200438

Actively Recruiting

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Research Team

Y

Yu Liu, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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