NCT07160413

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
8mo left

Started Sep 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress52%
Sep 2025Dec 2026

First Submitted

Initial submission to the registry

August 29, 2025

Completed
3 days until next milestone

Study Start

First participant enrolled

September 1, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 8, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2025

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Expected
Last Updated

September 12, 2025

Status Verified

September 1, 2025

Enrollment Period

4 months

First QC Date

August 29, 2025

Last Update Submit

September 8, 2025

Conditions

Keywords

Peripheral nerve stimulationMagnetic and electric stimulationSensitivity of nerves to magnetic fields

Outcome Measures

Primary Outcomes (1)

  • Maximum nerve activation response to electromagnetic stimulation with different coils

    Maximum 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.

    Day 1

Secondary Outcomes (3)

  • Spatial range of nerve activation with electromagnetic coils

    Day 1

  • Spatial range of nerve activation with neuromuscular electrical stimulation electrodes (NMES)

    Day 1

  • Amplitude ratios of temporal interference stimulation (TIS) electrodes associated with nerve activation

    Day 1

Study Arms (1)

Stimulated

EXPERIMENTAL
Device: Electric and electromagnetic stimulation

Interventions

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

Stimulated

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Institute for Human Centered Engineering HuCE

Biel, Biel, 2502, Switzerland

RECRUITING

Central Study Contacts

Thomas Niederhauser, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Prof. Dr.

Study Record Dates

First Submitted

August 29, 2025

First Posted

September 8, 2025

Study Start

September 1, 2025

Primary Completion

December 31, 2025

Study Completion (Estimated)

December 31, 2026

Last Updated

September 12, 2025

Record last verified: 2025-09

Locations