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Peripheral Nerve Activation Sensitivity

Peripheral Nerve Activation Sensitivity to Electromagnetic and Electrical Stimulation in the Upper Arm

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07160413
Acronym
PERNEAC
Enrollment
50
Registered
2025-09-08
Start date
2025-09-01
Completion date
2026-12-31
Last updated
2025-09-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nerve Excitation Sensitivity

Keywords

Peripheral nerve stimulation, Magnetic and electric stimulation, Sensitivity of nerves to magnetic fields

Brief summary

Volunteers will undergo various peripheral nerve stimulations (electric, electromagnetic, and temporal interference) to evaluate each method's sensitivity. The main objective is to examine the relationship between nerve activation and coil placement relative to the nerve, as well as how different coil types influence maximal nerve activation.

Interventions

DEVICEElectric and electromagnetic stimulation

Application of electromagnetic and electric stimulation using coils of different designs and electrodes to assess peripheral nerve sensitivity. The stimulation is momentary, non-therapeutic, and performed for basic science research purposes

Sponsors

Bern University of Applied Sciences
CollaboratorOTHER
Swiss Paraplegic Research, Nottwil
CollaboratorNETWORK
Thomas Niederhauser
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Person aged \> 18 years * Signed informed consent * Healthy * Willingness and ability to adhere to study procedures

Exclusion criteria

* Known hypersensitivity to electric or electromagnetic stimulation * Any implanted metal or electronic device in the upper body (except dental work such as fillings or braces), e.g., active medical devices, metal implants * Neurological or neuromuscular disorders or conditions * History of seizures or epilepsy * Current treatment with drugs that lower seizure threshold (e.g., certain analgesics, methylxanthines, antipsychotics, antidepressants, antiepileptics, anesthetics) * Pregnancy or breastfeeding * Surgical intervention of the arm within the last 4 weeks * Allergy to adhesives or ultrasound gel components (e.g., polyethylene glycols) * Skin lesions, infections, or strictures in the arm region * Tattoos on the stimulated (right) arm and hand, or in any area likely to be captured in video recordings * Inability to follow study procedures (e.g., due to language barrier, psychological disorders, dementia) * Participant deprived of liberty by administrative or judicial decision or under legal guardianship

Design outcomes

Primary

MeasureTime frameDescription
Maximum nerve activation response to electromagnetic stimulation with different coilsDay 1Maximum of the measured signals (muscle contraction from electromyography (EMG) and finger movement from accelerometer) obtained across all stimulation positions at a given stimulation intensity for each coil type. This reflects the relative sensitivity of peripheral nerves to electromagnetic stimulation with different coil designs.

Secondary

MeasureTime frameDescription
Spatial range of nerve activation with electromagnetic coilsDay 1Distance around the stimulation position yielding the maximum response (E1), within which the measured signals (muscle contraction and finger movement) remain at least 50% of the maximum, across all coil positions at a given stimulation intensity.
Spatial range of nerve activation with neuromuscular electrical stimulation electrodes (NMES)Day 1Distance around the stimulation position yielding the maximum response, within which the measured signals (muscle contraction and finger movement) remain at least 50% of the maximum, across all NMES electrode positions at a given stimulation intensity.
Amplitude ratios of temporal interference stimulation (TIS) electrodes associated with nerve activationDay 1Electrode amplitude ratios during Temporal Interference Stimulation (TIS) for which measured signals remain at least 50% of the maximum signals observed at the optimal position.

Countries

Switzerland

Contacts

Primary ContactThomas Niederhauser, PhD
thomas.niederhauser@bfh.ch+41 32 321 67 63

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026