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Sleep, energy and the brain

Transcutaneous auricular vagus nerve stimulation (taVNS) improves sleep quality in chronic insomnia disorder: A double-blind, randomized, sham-controlled trial.

3 Small study in people

What this means for you: first signals, nothing more.
Type of study
controlled trial
Studied in
people
Participants
40
Published
2025 in Sleep medicine
Cited
7 times by other research
Who paid
Not declared. PubMed carries no conflict-of-interest statement for most articles; that is not the same as independent.
Source
PubMed 40398066 · doi 10.1016/j.sleep.2025.106579
The plain-language write-up of this study is still being written. Below is the abstract exactly as the researchers published it.
Abstract by the researchers — original text

BACKGROUND: Insomnia is a common sleep disorder that significantly impacts quality of life and health. Conventional treatments such as cognitive-behavioral therapy and pharmacological interventions have limitations, underscoring the need for non-invasive alternatives. Transcutaneous auricular vagus nerve stimulation (taVNS) has emerged as a promising therapy to enhance sleep quality by modulating the autonomic nervous system. OBJECTIVE: This study aimed to evaluate the efficacy and safety of taVNS compared to sham in managing chronic insomnia disorder. METHODS: A randomized, double-blind, sham-controlled trial was conducted with 40 participants diagnosed with chronic insomnia disorder. Participants were randomly assigned to receive taVNS or sham for 30 min daily over six weeks. Sleep quality was assessed using the Pittsburgh Sleep Quality Index (PSQI) as the primary outcome. Secondary outcomes included the Insomnia Severity Index (ISI), World Health Organization Quality of Life Brief Version (WHOQOL-BREF), and total sleep time. Adverse events were recorded, and objective sleep measures were obtained using Fitbit wearable devices. RESULTS: In the modified intention-to-treat analysis at 6 weeks, the taVNS group exhibited significantly greater reductions in PSQI scores compared to the sham group (mean change: 4.5 ± 3.55 vs. -1.9 ± 2.15; Cohen's d = -1.21; p = .009). ISI scores also improved more in the taVNS group (-7.6 ± 5.23 vs. -4.25 ± 3.48; Cohen's d = -.75; p = .023). Total sleep time increased significantly in the taVNS group (584 ± 1015 min, vs. -10.8 ± 579 min; Cohen's d = .69; p = .019) and improved quality of life (WHOQOL-BREF: 32.2 ± 40.9 vs. 7.95 ± 33.5; Cohen's d = .65, p = .047). No significant adverse events were reported. CONCLUSIONS: taVNS significantly improved sleep quality, insomnia severity, and overall quality of life compared to sham. These findings establish taVNS as a safe and effective non-invasive therapy for managing insomnia, with potential for broader clinical applications.