Testing Non-Invasive Spinal Stimulation Devices

Recruiting now · Not applicable

Conditions studied: Healthy Participants

In brief

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 facts

Study ID

NCT07217314

Run by

Gail Forrest

People needed

10

Starts

2025-05-29

Expected to finish

2029-01-01

Last updated by the study team

2026-05-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• At least 18 years of age
• Proficient in English
• Available for the testing session
• Able to give informed consent
• Able to tolerate spinal stimulation

You may not qualify if…

• Pregnant (female only).
• Untreated severe and persistent problems regulating blood pressure, heart rate, or other automatic functions.
• Any past or present injury or disease to the nervous system
• Heart or lung disease that may interfere with stimulation
• A skin condition in any area that may affect the ability to receive stimulation
• Taking any medication that may affect the ability to receive spinal stimulation
• Ongoing drug abuse

Where it is running

• Kessler Foundation — West Orange, New Jersey, United States (enrolling)

Full record on ClinicalTrials.gov

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