6 Participants NeededMy employer runs this trial

Transcranial Magnetic Stimulation for Motor Deficits After Brain Tumor Surgery

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Overseen ByResearch Nurse Navigator
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

When doctors perform surgery to remove brain tumors, the goal is to take out as much of the tumor as possible while keeping the patient's brain functions intact. However, sometimes patients have trouble with movements like walking or using their hands after surgery. One reason for this is unintentional damage to important areas of the brain during the operation. A technique called Transcranial Magnetic Stimulation (TMS) might help patients recover these lost abilities faster.

The investigators are conducting a study to see if TMS can help patients recover their movement abilities after brain tumor surgery. TMS uses magnetic pulses to stimulate specific parts of the brain. In this study, the investigators will treat six patients with TMS once per day for three days in a row. Three patients with recent movement difficulties one to two weeks after surgery will be recruited for this study; they will also receive physical therapy. An additional three patients with persisting movement difficulties up to three years after tumor surgery will also be recruited for this study, regardless of whether or not they receive physical therapy.

The investigators will use two standard tests to see how well patients can move before and after the TMS treatment. These tests will help the investigators understand if TMS is making a difference in their recovery.

Who Is on the Research Team?

BJ

Brian J Gill, MD

Principal Investigator

Columbia University

Are You a Good Fit for This Trial?

Inclusion Criteria

I have had surgery and still have movement problems for less than three years.
I have had treatments before, except for TMS therapy.
Ability to understand and the willingness to sign a written informed consent document.
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Exclusion Criteria

Pregnant or breast-feeding individuals.
Patients with implanted devices (e.g., pacemakers, implanted stimulators, intracranial electrodes, cochlear implants).
Active suicidal ideation or plan as assessed by the Columbia Suicide Severity Rating Scale.
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Treatment

Participants receive TMS treatment once per day for three consecutive days

1 week
3 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

6 months
Visits at 1 week, 1 month, 3 months, and 6 months post-intervention

What Are the Treatments Tested in This Trial?

Interventions

  • Transcranial Magnetic Stimulation (TMS)

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Transcranial magnetic stimulationExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Brian J.Gill

Lead Sponsor

Columbia University

Collaborator

Trials
1,529
Recruited
2,832,000+