Could a gentle zap to the neck ease long COVID fatigue?
NCT ID NCT05445427
First seen Jun 27, 2026 · Last updated Sep 10, 2026 · Updated 2 times
Summary
This pilot study tested whether a non-invasive vagus nerve stimulator can help people with post-COVID syndrome who suffer from fatigue and headaches. Eighteen participants used the device, and researchers measured changes in their functional status and fatigue levels. The goal is to see if this simple, drug-free approach can improve daily life for those with lingering COVID symptoms.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- non-invasive vagus nerve stimulator
- What this could lead to
- If it works, this could point toward a simple, drug-free way to manage lingering fatigue and headaches after COVID-19.
- What could go wrong
- This is a very small pilot study with only 18 people, so results may not apply widely. The device may not work better than a placebo, and benefits could be minor.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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18 people
The number who actually took part.
- Started
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Dec 2022
- Finished
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Mar 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Presence of fatigue and post exertional malaise. * Presence of headache * Clinical diagnosis of post COVID syndrome. * They have consented to participate in the study * They have the ability to participate in all aspects of the study. Exclusion Criteria: * Pregnant. * Prior adverse reaction to 14FDG. * Active implantable medical device e.g. pacemaker, hearing aid implant * Metallic device e.g. stent, orthopedic hardware in neck * Using another electronic device at the same time e.g. TENS, mobile phone. * Any other condition deemed exclusionary by the study principal investigator
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Mayo Clinic in Rochester
Rochester, Minnesota, 55905, United States
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