Zap to the arm may get blood pumping – small study tests the idea
NCT ID NCT07354607
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study is testing whether transcutaneous electrical nerve stimulation (TENS) – a gentle electrical pulse on the skin – can increase blood flow in the arm. Thirty-six healthy adults will try six different stimulation settings to see which works best. The goal is to find the optimal frequency and electrode placement for the strongest blood flow response.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- transcutaneous electrical nerve stimulation (TENS)
- What this could lead to
- If successful, this could point toward a non-drug way to improve blood flow, possibly helping people with circulation problems.
- What could go wrong
- This is a very early, small pilot study in healthy volunteers, not patients. It only tests short-term effects, so real-world benefits are uncertain.
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
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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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About 36 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- 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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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subject aged 18 years or older * Having freely given written consent, after being informed of the purpose of the study, its conduct and its risks. * Affiliated with a social security scheme Exclusion Criteria: * Persons with pacemakers or any other implantable electrical devices, * Pregnant women * Suffering from dermatological conditions or muscle/skin lesions on the arms and forearms. * Participant unable to give free and informed consent. * Participant unable to comply with the specific procedures of the study. * Participant deprived of liberty or benefiting from legal protection measures.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Centre Hospitalier Métropole Savoie
RECRUITINGChambéry, 73000, France
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