Clinical Trials Directory

Trials / Completed

CompletedNCT04384965

Accelerated iTBS for Depressed Patients During the COVID-19 Pandemic

A Novel and Practical Accelerated Intermittent Theta Burst Protocol as a Substitute for Depressed Patients Needing Electroconvulsive Therapy During the COVID-19 Pandemic

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
176 (actual)
Sponsor
Centre for Addiction and Mental Health · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The current study aims to assess the feasibility, acceptance and clinical outcomes of a practical high-dose aiTBS protocol, including tapering treatments and symptom-based relapse prevention treatments, in patients with unipolar depression previously responsive to ECT and patients needing urgent treatment due to symptom severity during the COVID-19 pandemic.

Conditions

Interventions

TypeNameDescription
DEVICEMagPro X100 Stimulator, B70 Fluid-Cooled CoilTreatment will occur 8 times per treatment day (50 min pause between treatments). Each treatment session will consist of a single iTBS treatment, delivering 600 pulses of iTBS (bursts of 3 pulses at 50 Hz, bursts repeated at 5 Hz, with a duty cycle of 2 seconds on, 8 seconds off, over 60 cycles / \~3 minutes) at a target of 110% of the subject's resting MT.

Timeline

Start date
2020-05-12
Primary completion
2022-05-18
Completion
2022-11-01
First posted
2020-05-12
Last updated
2024-02-20

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT04384965. Inclusion in this directory is not an endorsement.