Transcranial Magnetic Stimulation in Progressive Supranuclear Palsy

  • STATUS
    Recruiting
  • End date
    Jun 5, 2026
  • participants needed
    30
  • sponsor
    Oregon Health and Science University
Updated on 19 February 2024
transcranial magnetic stimulation
dopamine
progressive supranuclear palsy
speech therapy

Summary

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 by increasing functional connectivity between the cerebellum, thalamus, and primary motor cortex.

Details
Condition Progressive supranuclear palsy, Palsy Supranuclear
Age 40-85 years
Treatment Repetitive transcranial magnetic stimulation (rTMS)
Clinical Study IdentifierNCT04468932
SponsorOregon Health and Science University
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

probable or possible PSP by the revised MDS PSP Criteria (Hoglinger 2017)
age 40-85 at time of screening
ability to understand and cooperate with simple instructions in English
ability to read at 6th grade reading level in English
ability to tolerate balance testing with a safety harness
ability to refrain from other physical and speech therapy programs for the duration for the study
ability to remain on stable doses of any cholinergic, dopaminergic, serotonergic sedative or NMDA receptor antagonists for the duration of the study
females of child-bearing age must perform a urine pregnancy test and be on reliable birth control during the course of the study

Exclusion Criteria

other significant neurological or vestibular disorders
presence of electrically, magnetically or mechanically activated implants or history of injurious metal exposure in eyes, head, or body
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.