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NCT05669508 · ClinicalTrials.gov registry record · NA

Wearable Electrical Stimulation on the Back to Modulate Spinal Cord Activity

A NA study of Spinal Cord Injuries and Spinal Cord Diseases, sponsored by Thomas Jefferson University.

Active
Registry status
NA
Development phase
4
Enrollment target
1
Study location

NCT05669508 is a NA study of Spinal Cord Injuries and Spinal Cord Diseases that is active but no longer recruiting, run by Thomas Jefferson University. The registered enrollment target is 4 participants, below the 62-participant average among 202 other Spinal Cord Injuries trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05669508, a NA study of Spinal Cord Injuries and Spinal Cord Diseases, is active but no longer recruiting, sponsored by Thomas Jefferson University.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
4 participants
Enrollment target
1
Study location

Study Summary

The goal of this study is to evaluate if non-invasive electrical spinal stimulation can help people with paralysis caused by SCI improve strength and function of their arms, legs, hands or feet. The study will involve therapy sessions involving exercises done at the same time as electrical stimulation therapy. This study has multiple parts to evaluate the effectiveness and safety of "smart" electrical stimulation of the spinal cord, which involves stimulating the spinal cord at precise locations and times to improve movement and function.

Interventions

  • DEVICE RISES-T System
  • OTHER Occupational/Physical Therapy

Study Locations (1)

Pennsylvania

  • Thomas Jefferson University - Philadelphia

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2022-02-10
Est. Completion 2026-12-31
Phase NA

Sponsor

Thomas Jefferson University

292 total trials

What the Registry Record Tells You About NCT05669508

The ClinicalTrials.gov registry entry for NCT05669508 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 4 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 62-participant average among 202 other Spinal Cord Injuries trials with a reported enrollment target (94% lower). The listed sponsor is Thomas Jefferson University, which has 292 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Spinal Cord Injuries appearing as the primary indexed condition, and to 2 interventions - of which RISES-T System is the first listed.

NCT05669508 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT05669508 about?

NCT05669508 is a clinical study titled "Wearable Electrical Stimulation on the Back to Modulate Spinal Cord Activity". The goal of this study is to evaluate if non-invasive electrical spinal stimulation can help people with paralysis caused by SCI improve strength and function of their arms, legs, hands or feet. The study will involve therapy sessions involving exercises done at the same time as electrical stimulati...

What is the current status of trial NCT05669508?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 4 participants. The study started on 2022-02-10. Estimated completion is 2026-12-31.

What conditions does trial NCT05669508 study?

This clinical trial studies the following conditions: Spinal Cord Injuries, Spinal Cord Diseases.

What interventions are being tested in trial NCT05669508?

The interventions under investigation include: RISES-T System (DEVICE), Occupational/Physical Therapy (OTHER).

Who is sponsoring clinical trial NCT05669508?

This trial is sponsored by Thomas Jefferson University, which has 292 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05669508 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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