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Non-Invasive Stimulation for Improving Motor Function

NCT03592173 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2024-08-06

No results posted yet for this study

Summary

The purpose of this study is to determine if spinal excitability is increased with a Spinal Associative Stimulation (SAS) protocol, and to determine the functional consequences of this technique on motor recovery.

Conditions

  • Spinal Cord Injuries

Interventions

DIAGNOSTIC_TEST

Paired TMS & Peripheral Nerve Stimulation

Method of assessing neurophysiology and activity of the spinal cord

Sponsors & Collaborators

  • Burke Medical Research Institute

    collaborator OTHER

  • Kathleen Friel

    lead OTHER

Principal Investigators

  • Kathleen Friel, PhD · Burke Medical Research Institute

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2025-09-30
Completion
2025-12-31
FDA Device
Yes

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 NCT03592173 on ClinicalTrials.gov