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

Part of paid clinical trials in Palo Alto, California.

Sponsor
VA Palo Alto Health Care System
Study ID
NCT06140706
Status
Not Yet Recruiting

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Conditions

  • Tetraplegia

Eligibility Criteria

Sex
ALL
Age
18 Years - 75 Years
Healthy Volunteers
Not accepted

Interventions

  • transcutaneous Spinal Cord Stimulation (tSCS) — BEHAVIORAL
    Neurostimulation for upper extremity training, delivered through video telehealth, 8 weeks of home use for (i) feasibility and (ii) potential functional improvement.

Study Details

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.

Key Dates

Start date
Sep 1, 2025
Status verified
Apr 2025
Primary completion
Dec 31, 2027
Completion
Dec 31, 2027

Study Design

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

Arms

  • Experimental: tSCS plus home tele-video support
    Cervical transcutaneous spinal stimulation during home tele-video visits

Primary Outcome Measure

NASA-TLX (NASA Task Load Index) [ Time Frame: At 8 weeks (after completion of home program) ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
VA Palo Alto Health Care SystemPalo AltoCalifornia94304-

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VA Palo Alto Health Care System· Palo Alto, CA

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