@article{d36ab8e078164046963a8dd34f8f280d,
title = "Left prefrontal transcranial magnetic stimulation for treatment-resistant depression in adolescents: a double-blind, randomized, sham-controlled trial",
abstract = "Treatment-resistant depression (TRD) is prevalent and associated with a substantial psychosocial burden and mortality. There are few prior studies of interventions for TRD in adolescents. This was the largest study to date examining the feasibility, safety, and efficacy of 10-Hz transcranial magnetic stimulation (TMS) for adolescents with TRD. Adolescents with TRD (aged 12–21 years) were enrolled in a randomized, sham-controlled trial of TMS across 13 sites. Treatment resistance was defined as an antidepressant treatment record level of 1 to 4 in a current episode of depression. Intention-to-treat patients (n = 103) included those randomly assigned to active NeuroStar TMS monotherapy (n = 48) or sham TMS (n = 55) for 30 daily treatments over 6 weeks. The primary outcome measure was change in the Hamilton Depression Rating Scale (HAM-D-24) score. After 6 weeks of blinded treatment, improvement in the least-squares mean (SE) HAM-D-24 scores were similar between the active (−11.1 [2.03]) and sham groups (−10.6 [2.00]; P = 0.8; difference [95% CI], − 0.5 [−4.2 to 3.3]). Response rates were 41.7% in the active group and 36.4% in the sham group (P = 0.6). Remission rates were 29.2% in the active group and 29.0% in the sham group (P = 0.95). There were no new tolerability or safety signals in adolescents. Although TMS treatment produced a clinically meaningful change in depressive symptom severity, this did not differ from sham treatment. Future studies should focus on strategies to reduce the placebo response and examine the optimal dosing of TMS for adolescents with TRD.",
author = "Croarkin, {Paul E.} and Elmaadawi, {Ahmed Z.} and Aaronson, {Scott T.} and Schrodt, {G. Randolph} and Holbert, {Richard C.} and Sarah Verdoliva and Heart, {Karen L.} and Demitrack, {Mark A.} and Strawn, {Jeffrey R.}",
note = "Funding Information: The study was funded by Neuronetics. Mayo Clinic does not endorse specific products or services included in this article. Dr Croarkin has received research support from the National Institute of Mental Health, Neuronetics, and NeoSync, Inc. He has received material support from and provided consultation to Myriad Genetics. He has consulted for Procter & Gamble Co. Dr Elmaadawi receives research support from Duke University and the University of Northwestern. He receives research funding from Neurocrine, Inc, and Neuronetics. Dr Aaronson has received research support from Compass and Neuronetics and serves as a consultant to LivaNova PLC, Neuronetics, Janssen, Sage Therapeutics, and Genomind, Inc. He serves on speaker boards for Janssen and Sunovion Pharmaceuticals, Inc. Dr Holbert has received material support (equipment) from Neuronetics. He is also a speaker for Neuronetics. Ms Heart is an employee of Neuronetics. Dr Demitrack is a consultant to Neuronetics and a full-time employee of Trevena, Inc. Dr Strawn has received research support from Allergan, Neuronetics, Otsuka Pharmaceutical Co, Ltd, National Institute of Mental Health, National Institute of Child Health and Human Development, National Institute of Environmental Health Sciences, and the Yung Family Foundation. He receives royalties from Springer Publishing Co and has received honoraria from CMEology and Neuroscience Education Institute. He receives royalties from UpToDate. He has received material support from and provided consultation to Myriad Genetics. The other authors have no disclosures. The authors declare no competing interests. Publisher Copyright: {\textcopyright} 2020, The Author(s), under exclusive licence to American College of Neuropsychopharmacology.",
year = "2021",
month = jan,
doi = "10.1038/s41386-020-00829-y",
language = "English (US)",
volume = "46",
pages = "462--469",
journal = "Neuropsychopharmacology",
issn = "0893-133X",
publisher = "Nature Publishing Group",
number = "2",
}