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Transcranial Magnetic Stimulation

Transcranial magnetic stimulation (TMS) for Chemobrain

N/A
Waitlist Available
Led By Phillip Kuo, MD
Research Sponsored by University of Arizona
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 14 days
Awards & highlights

Study Summary

This trial will test if a treatment called rTMS can help people with PCCI. The study will use tests to measure how well the treatment works.

Eligible Conditions
  • Chemobrain

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~two weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and two weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Memory Testing
Secondary outcome measures
Test for improved brain functional connectivity on fMRI.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Transcranial magnetic stimulation (TMS)Experimental Treatment1 Intervention
We propose to test the efficacy of rTMS for the treatment of PCCI. Efficacy measures will include baseline and post-rTMS neuropsychological testing, functional MRI and biometry data using body worn sensors.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Transcranial magnetic stimulation (TMS)
2013
Completed Phase 4
~510

Find a Location

Who is running the clinical trial?

University of ArizonaLead Sponsor
514 Previous Clinical Trials
148,593 Total Patients Enrolled
Phillip Kuo, MDPrincipal InvestigatorUniversity of Arizona

Frequently Asked Questions

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~0 spots leftby Apr 2025