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Feasibility of Home Based Transcutaneous Spinal Cord Stimulation for Persons With SCI

NCT06140706 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2025-04-10

No results posted yet for this study

Summary

The proposed study will focus on the feasibility of and effectiveness to a home-based program for persons with chronic SCI focused on upper limb training augmented with a transcutaneous neurostimulator supported via a video telehealth platform.

Conditions

  • Tetraplegia

Interventions

BEHAVIORAL

transcutaneous Spinal Cord Stimulation (tSCS)

Neurostimulation for upper extremity training, delivered through video telehealth, 8 weeks of home use for (i) feasibility and (ii) potential functional improvement.

Sponsors & Collaborators

  • ONWARD Medical, Inc.

    collaborator INDUSTRY

  • VA Palo Alto Health Care System

    lead FED

Principal Investigators

  • Jenny Kiratli, PhD · VA Palo Alto Health Care System

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-01
Primary Completion
2027-12-31
Completion
2027-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06140706 on ClinicalTrials.gov