» Articles » PMID: 25767458

Rethinking the Role of Sham TMS

Overview
Journal Front Psychol
Date 2015 Mar 14
PMID 25767458
Citations 89
Authors
Affiliations
Soon will be listed here.
Abstract

Sham transcranial magnetic stimulation (TMS) approaches are widely used in basic and clinical research to ensure that observed effects are due to the intended neural manipulation instead of being caused by various possible side effects. We here critically discuss several methodological aspects of sham TMS. Importantly, we propose to carefully distinguish between the placebo versus sensory side effects of TMS. In line with this conceptual distinction, we describe current limitations of sham TMS approaches in the context of placebo effects and blinding success, followed by a short review of our own work demonstrating that the sensory side effects of sham TMS are not unspecific as often falsely assumed. Lastly, we argue that sham TMS approaches are inherently insufficient as full-fledged control conditions as they fail to demonstrate the specificity of TMS effects to a particular brain area or time point of stimulation. Sham TMS should therefore only complement alternative control strategies in TMS research.

Citing Articles

Effects of parietal iTBS on resting-state effective connectivity within the frontoparietal network in patients with schizophrenia: An fMRI study.

Li L, Wang L, Wu H, Li B, Pan W, Jin W Neuroimage Clin. 2024; 45:103715.

PMID: 39608227 PMC: 11638604. DOI: 10.1016/j.nicl.2024.103715.


Online transcranial magnetic stimulation reveals dynamic interactions between language control and processing in bilingual language production.

Wu J, Ji Y, Cai C, Pu X, Wang Q, Yan G Cereb Cortex. 2024; 34(11).

PMID: 39604075 PMC: 11602258. DOI: 10.1093/cercor/bhae452.


Preliminary findings of a randomized controlled trial investigating the efficacy of transcranial magnetic stimulation in treatment-resistant depression: a analysis on the role of co-occurring personality disorders.

Maciaszek J, Rymaszewska J, Wieczorek T, Piotrowski P, Szczesniak D, Beszlej J Front Psychiatry. 2024; 15:1363984.

PMID: 39588550 PMC: 11586332. DOI: 10.3389/fpsyt.2024.1363984.


Adaptation and exogenous attention interact in the early visual cortex: A TMS study.

Lee H, Fernandez A, Carrasco M iScience. 2024; 27(11):111155.

PMID: 39524352 PMC: 11544076. DOI: 10.1016/j.isci.2024.111155.


Meta-learning of human motor adaptation via the dorsal premotor cortex.

Sugiyama T, Uehara S, Izawa J Proc Natl Acad Sci U S A. 2024; 121(44):e2417543121.

PMID: 39441634 PMC: 11536165. DOI: 10.1073/pnas.2417543121.


References
1.
Counter S, Borg E . Analysis of the coil generated impulse noise in extracranial magnetic stimulation. Electroencephalogr Clin Neurophysiol. 1992; 85(4):280-8. DOI: 10.1016/0168-5597(92)90117-t. View

2.
Segev A, Bloch Y . A bit of shame and a proud sham. Brain Stimul. 2012; 6(4):703-4. DOI: 10.1016/j.brs.2012.11.002. View

3.
Broadbent H, Van Den Eynde F, Guillaume S, Hanif E, Stahl D, David A . Blinding success of rTMS applied to the dorsolateral prefrontal cortex in randomised sham-controlled trials: a systematic review. World J Biol Psychiatry. 2011; 12(4):240-8. DOI: 10.3109/15622975.2010.541281. View

4.
Duecker F, Sack A . Pre-stimulus sham TMS facilitates target detection. PLoS One. 2013; 8(3):e57765. PMC: 3587629. DOI: 10.1371/journal.pone.0057765. View

5.
Lisanby S, GUTMAN D, Luber B, Schroeder C, Sackeim H . Sham TMS: intracerebral measurement of the induced electrical field and the induction of motor-evoked potentials. Biol Psychiatry. 2001; 49(5):460-3. DOI: 10.1016/s0006-3223(00)01110-0. View