What is the efficacy of Transcranial Magnetic Stimulation (TMS) for treating Post-Traumatic Stress Disorder (PTSD)?

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Last updated: March 31, 2025View editorial policy

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From the Guidelines

Transcranial Magnetic Stimulation (TMS) is not recommended as a first-line treatment for Post-Traumatic Stress Disorder (PTSD) due to limited evidence supporting its effectiveness for this specific condition. According to the most recent study 1, there were no significant differences in outcomes between repetitive TMS (rTMS) and sham therapies in patients with PTSD, suggesting that placebo effects may play a significant role in rTMS outcomes.

Key Considerations

  • The study found that the benefits of rTMS for treatment-resistant depression (TRD) outweigh the harms, but this does not necessarily apply to PTSD 1.
  • Other treatments, such as medication and psychotherapy, have shown efficacy in treating PTSD, with selective serotonin reuptake inhibitors (SSRIs) like fluoxetine, sertraline, and paroxetine demonstrating effectiveness in reducing symptoms 1.
  • Brief cognitive-behavioral therapy (CBT) has also been shown to speed recovery and prevent the development of chronic PTSD in some studies 1.

Treatment Options

  • Medications like SSRIs are considered first-line treatments for PTSD, with studies showing that they can reduce symptoms and improve quality of life 1.
  • Psychotherapy, including CBT and exposure therapy, is also a recommended treatment option, with evidence supporting its effectiveness in reducing symptoms and improving outcomes 1.
  • TMS may be considered as an adjunctive treatment or for patients who have not responded to other treatments, but its use for PTSD is currently off-label and requires further research to fully understand its effectiveness.

From the Research

Transcranial Magnetic Stimulation (TMS) for PTSD

  • TMS has emerged as a noninvasive neuromodulatory intervention for psychiatric disorders, including PTSD, with mounting evidence for its safety, tolerability, and efficacy 2.
  • The majority of studies utilize repetitive TMS targeted to the right dorsolateral prefrontal cortex (DLPFC) at low frequency (1 Hz) or high frequency (10 or 20 Hz) 2.
  • High-frequency TMS applied to the left DLPFC has been shown to be more effective in PTSD rating scales posttreatment than low-frequency stimulation 3.
  • A meta-analysis found an overall effect size of d = 1.17,95% CI [0.89 - 1.45] for TMS as a treatment for PTSD, with high frequency TMS showing a significantly larger treatment effect compared to low frequency 4.

Efficacy and Safety of TMS for PTSD

  • TMS appears to be safe and effective for PTSD, with effects often sustained for up to 2-3 months 2.
  • The most common side effect of TMS is headache and scalp pain, treated by mild analgesics, while seizures are a rare side effect 3.
  • More research is needed to understand the neurological mechanisms of TMS on specific PTSD symptoms and to design more effective treatment for individuals 4.

Comparison with Other Treatments for PTSD

  • SSRIs, such as sertraline, paroxetine, and fluoxetine, are the most studied medications for PTSD and are considered first-line treatment 5.
  • Non-SSRIs, such as venlafaxine, and other medications may be considered as second-line or third-line treatment for PTSD 5, 6.
  • TMS may be considered as an alternative treatment for PTSD, particularly for individuals who have failed to respond to first-line psychotherapies and pharmacotherapy 2.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Transcranial magnetic stimulation for post-traumatic stress disorder.

Therapeutic advances in psychopharmacology, 2021

Research

Evidence-based prescribing for post-traumatic stress disorder.

The British journal of psychiatry : the journal of mental science, 2020

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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