ORCID: https://orcid.org/0000-0003-3965-5664; Blackwell, Simon E.
ORCID: https://orcid.org/0000-0002-3313-7084; Chen, Miaoxi
ORCID: https://orcid.org/0009-0007-3991-153X; Feldmann, Lisa
ORCID: https://orcid.org/0009-0002-3404-2869; Björklund, Jonas
ORCID: https://orcid.org/0000-0003-2521-6679; Dechantsreiter, Esther
ORCID: https://orcid.org/0009-0002-0674-4572; Bulubas, Lucia
ORCID: https://orcid.org/0000-0002-5797-8742; Goerigk, Stephan
ORCID: https://orcid.org/0000-0002-3021-0346; Keeser, Daniel
ORCID: https://orcid.org/0000-0002-0244-1024; Falkai, Peter
ORCID: https://orcid.org/0000-0003-2873-8667; Greimel, Ellen
ORCID: https://orcid.org/0000-0002-9916-9230; Bechmann, Peter; Schulte-Körne, Gerd
ORCID: https://orcid.org/0000-0002-9960-1572; Hasan, Alkomiet
ORCID: https://orcid.org/0000-0002-2662-9742; Strube, Wolfgang
ORCID: https://orcid.org/0000-0003-2380-7651 und Padberg, Frank
ORCID: https://orcid.org/0000-0001-7638-8310
(10. October 2024):
Intermittent theta burst stimulation in adolescents and young adults with depressive disorders: protocol of a randomized, sham-controlled study with a sequential Bayesian design for adaptive trials.
In: European Archives of Psychiatry and Clinical Neuroscience
Abstract
Intermittent theta burst stimulation (iTBS), a variant of repetitive transcranial magnetic stimulation (rTMS), is an established treatment for adults with major depressive disorder (MDD). Due to its favorable safety profile, iTBS is also a promising early intervention in the transition phase from adolescence to early adulthood, but this has not been systematically investigated to date. Thus, the EARLY-BURST trial investigates the efficacy and safety of iTBS over the left dorsolateral prefrontal cortex (lDLPFC) in treatment-seeking young patients (age 16–26 years) with depressive disorders (i.e. major depressive disorder, persistent depressive disorder, bipolar depression), allowing for relevant co-morbidities. Participants have not received antidepressant or antipsychotic medication during the last 12 months except for short-term (< 2 weeks) on-demand medication. The trial will employ a novel sequential Bayesian, randomized, double-blind, parallel-group, sham-controlled design. Up to 90 patients at two clinical sites (Munich, Augsburg) will be randomized 1:1 to the treatment groups, with sequential analyses starting after 26 patients in each group completed the treatment. The primary outcome will be the difference in depression severity at week 6 (post-treatment visit) between active iTBS and sham iTBS, assessed with the Montgomery-Åsberg Depression Rating Scale (MADRS). The trial is planned to be expanded towards a three-arm leapfrog design, contingent on securing additional funding. Thus, in addition to potentially providing evidence of iTBS’s efficacy in adolescents and young adults with depressive disorders, the EARLY-BURST trial aims at setting the stage for subsequent platform trials in this dynamic research field, where novel adaptive study designs are required to meet the need for rapidly testing promising new vs established rTMS protocols.
Trial registration: DRKS00033313.
| Item Type: | Journal article |
|---|---|
| Faculties: | Medicine > Medical Center of the University of Munich > Clinic and Polyclinic for Psychiatry and Psychotherapy |
| Subjects: | 100 Philosophy and Psychology > 150 Psychology |
| ISSN: | 0940-1334 |
| Annotation: | Online first |
| Language: | English |
| Item ID: | 126272 |
| Date Deposited: | 12. Jun 2025 09:24 |
| Last Modified: | 12. Jun 2025 09:24 |
