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
| Type | Name | Description |
|---|---|---|
| DEVICE | MagPro X100 Stimulator, B70 Fluid-Cooled Coil | Treatment 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.