Intensive TMS for Rapid Relief of Bipolar Depression Symptoms

University of Pennsylvania1 site in 1 country34 target enrollmentMarch 1, 2022

Overview

Brief Summary

The research study is being conducted to test whether using high dose spaced theta-burst rTMS (a form of transcranial magnetic stimulation) produces a significant reduction in depressive symptoms compared with sham. This project will recruit patients aged 18-70 with symptoms of bipolar depression who have failed (or not shown signs of improvement) after at least two prior treatments.

Detailed Description

The research study is being conducted to test whether using high dose spaced theta-burst rTMS (a form of transcranial magnetic stimulation) produces a significant reduction in depressive symptoms compared with sham. This project will recruit patients aged 18-70 with symptoms of bipolar depression who have failed (or not shown signs of improvement) after at least two prior treatments. The null hypothesis is that there will be no difference in reductions in depressive symptoms by the end of a five-day treatment period. The alternative hypothesis is that, compared with sham, active TMS will result in a greater reduction in depressive symptoms by the end of the treatment period. Participants will be randomly assigned to active or sham conditions: 50% to active and 50% to sham.

Registry

clinicaltrials.gov

Start Date

March 1, 2022

End Date

February 19, 2024

Last Updated

last year

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

University of Pennsylvania

Responsible Party

Principal Investigator

Yvette Sheline

McLure Professor of Radiology, Neurology and Psychiatry

University of Pennsylvania

Eligibility Criteria

Inclusion Criteria

•Bipolar depression (BP I and BP II) by Diagnostic and Statistical Manual 5 (DSM 5) criteria
•Age 18-70
•Right or left handed
•All genders
•Treatment resistant depression, as in they must have treatment resistant depression with 2 or more prior antidepressant trials that have failed to produce a response (\> 50% reduction in symptoms) using ATHF criteria
•Able to provide informed consent to participate in the study
•Must be on a stable medication regimen, requiring at least one mood stabilizer
•Depression severity as represented by scoring at least 20 on Montgomery-Asberg Depression Rating Scale (MADRS)

Exclusion Criteria

•No current substance abuse disorder for the past 6 months (previous substance abuse not exclusionary)
•Any psychotic disorder or current active psychotic symptoms (personality disorders not exclusionary unless in the opinion of the referring psychiatrist it would jeopardize participation)
•No dementia or other major neurological disorders
•Not having depression as primary disorder
•No major medical illness, for example metastatic cancer, end stage renal disease
•Not able to verify contact information. Participants must be able to follow through with the study \& must have verified contact information and at least one verified contact
•Pregnancy. While there are no known risks to a fetus this is a new use of TMS, which has not been tested, thus pregnancy is exclusionary
•Score on Young Mania Rating Scale (YMRS) greater than 12 (patients with mixed features have been shown not to respond well to TMS treatment)
•Rapid cycling Bipolar illness (patients with \> 4 mood episodes within the past year will be excluded, as they have a higher risk of switch to mania)
•Any implants, conditions, or contraindications that would be deemed unsafe for TMS or MRI

Outcomes

Primary Outcomes

Clinical Efficacy of High Dose Spaced Theta Burst (HDS-TBS)

Time Frame: Through study completion, approximately 1 week

The primary outcome will be based on the set of repeated Montgomery Asberg Depression scores (10 items rated on a 0-6 scale, 0-60 possible score range, with higher scores indicating greater depressive symptomology), obtained at baseline, on each of the five treatment days and post TMS.