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Electrical vestibular stimulation to improve balance in older adults: a pilot randomized controlled trial
Jordan A King1,2, Noah Walters3, Nadine Rodrigues3
1Department of Biomedical Engineering, University of Calgary, Calgary, AB, Canada.
Background:
Falls are the leading cause of injury-related hospitalizations among older adults, often linked to vestibular dysfunction. While vestibular rehabilitation therapy is a standard intervention, designed to compensate for vestibular impairment with proprioceptive and visual cues, potential cumulative effects of noisy Electrical Vestibular Stimulation (nEVS) on balance improvement in older adults are not well understood.
Objective:
This study evaluated the efficacy of cumulative nEVS dosing in improving static balance, its potential mechanisms, and clinical significance.
Methods:
A single-blind, pilot randomized controlled trial enrolled 40 older adults (mean age: 77.7 ± 11.8 years). Participants were randomly assigned to a Stimulation group (nEVS intervention) or Sham group. The nEVS regimen included low-amplitude wideband stimulation (± 0.35 mA, 0.001-300 Hz) for 20 min, three times weekly for six weeks. Balance performance was assessed immediately before and after nEVS using a head-mounted sensor to measure physiological vibration acceleration ('Phybrata') power as a measure of postural stability in four conditions: Floor Eyes Open, Floor Eyes Closed, Foam Eyes Open, and Foam Eyes Closed. Follow-ups occurred at 3 months and 6 months post-intervention.
Results:
The Stimulation group exhibited significant and sustained reductions in Phybrata power with improvements observed as early as Session 3 and persisting through 6 months in Foam EC. Additionally, the Sham group demonstrated smaller reductions in Phybrata power, potentially reflecting a learning effect.
Conclusion:
nEVS may be a safe and effective intervention for improving balance in older adults. Its benefits in addressing age-related deficits in balance and sensory integration highlight its potential for fall prevention and rehabilitation. This study was retrospectively registered as a clinical trial on February 25, 2025 (NCT06846047).
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