Non-invasive vestibular nerve stimulation (VeNS) reduces visceral adipose tissue: results of a randomised controlled trial
- PMID: 40082596
- PMCID: PMC11906803
- DOI: 10.1038/s41598-025-92744-9
Non-invasive vestibular nerve stimulation (VeNS) reduces visceral adipose tissue: results of a randomised controlled trial
Abstract
Across multiple species, chronic vestibular stimulation activates hypothalamic regions involved in energy homeostasis and reduces body fat. This first-in-human randomised controlled trial evaluated the efficacy and safety of electrical vestibular nerve stimulation (VeNS) as a means of reducing excess body weight and fat. Overweight and obese adults were randomised 1:1 to receive 60 min of daily VeNS (n = 117) or sham stimulation (n = 124) for 6 months, together with a hypocaloric diet. The primary endpoints were weight loss based. Secondary endpoints included reduction in visceral adipose tissue (VAT). It is VAT, more than subcutaneous fat depots, which is particularly associated with the risks associated with obesity. The weight loss based primary endpoints were not met. However, mean change in VAT was significantly greater in the active (- 12.6%) versus the sham (- 4.7%) group (p = 0.03). This suggests that regular VeNS may cause a clinically meaningful reduction in VAT.
Keywords: Galvanic stimulation; Neuromodulation; Obesity; Vestibular; Vestibular nerve stimulation; Visceral adipose tissue.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Competing interests: PDM is named as an inventor on various patents issued to the University of California that pertain to using vestibular stimulation to modify body mass composition. PDM and JM are co-founders of Neurovalens Ltd which is a company commercially developing vestibular stimulation as a treatment modality for a range of conditions including obesity. JM is CEO of Neurovalens and PDM is a director. SW is an employee of Neurovalens. No one in the Neurovalens team had any direct interaction with the clinical trial participants, nor were they involved in any aspects of trial execution, such as sample collection or measuring clinical outcomes. No other authors have competing interests.
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