Actively Recruiting

Phase Not Applicable
Age: 40Years - 85Years
All Genders
NCT04468932

Transcranial Magnetic Stimulation in Progressive Supranuclear Palsy

Led by Oregon Health and Science University · Updated on 2025-05-29

30

Participants Needed

1

Research Sites

378 weeks

Total Duration

On this page

Sponsors

O

Oregon Health and Science University

Lead Sponsor

N

National Center of Neuromodulation for Rehabilitation

Collaborating Sponsor

AI-Summary

What this Trial Is About

The objective of this proposal is to investigate the effect of non-invasive repetitive cerebellar transcranial magnetic stimulation (rTMS) on motor control in progressive supranuclear (PSP). The central hypothesis is that augmenting cerebellar inhibition via cerebellar rTMS will decrease postural instability in patients with PSP. We will use functional near infrared spectroscopy (fNIRS) to examine changes in motor and premotor cortical activity after cerebellar rTMS.

CONDITIONS

Official Title

Transcranial Magnetic Stimulation in Progressive Supranuclear Palsy

Who Can Participate

Age: 40Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Probable or possible progressive supranuclear palsy (PSP) by revised MDS PSP Criteria (Hoglinger 2017)
  • Age between 40 and 85 years at screening
  • Ability to understand and cooperate with simple instructions in English
  • Ability to read at a 6th grade reading level in English
  • Ability to stand unassisted for at least 30 seconds and walk independently with a walker
  • Ability to avoid starting new physical or speech therapy during the study
  • Ability to remain on stable doses of any cholinergic, dopaminergic, serotonergic sedative, or NMDA receptor antagonist medications during the study
  • Females of child-bearing age must have a negative urine pregnancy test and use reliable birth control during the study
Not Eligible

You will not qualify if you...

  • Other significant neurological or vestibular disorders
  • Presence of electrically, magnetically, or mechanically activated implants
  • History of injurious metal exposure in eyes, head, or body

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

Oregon Health & Science University

Portland, Oregon, United States, 97239

Actively Recruiting

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Research Team

G

Graham Harker

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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