Testing Non-Invasive Spinal Stimulation Devices

Part of paid clinical trials in West Orange, New Jersey.

Sponsor
Gail Forrest
Study ID
NCT07217314
Status
Recruiting

Conditions

  • Healthy Participants

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Spinal Stimulation — DEVICE
    Participants will lay on their back and have small electrodes placed on the center of their backs and several leg muscles. The back electrodes, connected to a battery-operated unit, will send an electrical current to the spine. The leg electrodes will record muscle activity. This will take approximately 4 hours to complete on each day. The 4 hours includes set-up/placement of the electrodes for each device, 4 trials of stimulation for each device with breaks, and removal of electrodes after testing on each device.

Study Details

The purpose of this study is to compare updated spinal stimulation devices with the spinal stimulation device that is currently used. Spinal stimulation is often used in studies aimed at assisting individuals with a spinal cord injury. These devices were updated to improve upon limitations in the currently used device. The devices will be compared in a group of people without spinal cord injury or other nervous system conditions.

Key Dates

Start date
May 29, 2025
Status verified
Aug 2025
Primary completion
Jan 31, 2027
Completion
Jan 31, 2029

Study Design

Enrollment
10 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER

Arms

  • Experimental: Healthy Participants

Primary Outcome Measure

Leg EMG activity during spinal stimulation [ Time Frame: up to 6 weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Kessler FoundationWest OrangeNew Jersey07052
Research Manager
9733243557
Gail F Forrest, PhD (PRINCIPAL_INVESTIGATOR)

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