Impact of Direct Current Electrical Stimulation on Treatment of Lumbosacral Radiculopathy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNeuFit - Neurological Fitness and Education

About this trial

This study will compare two methods of electrical stimulation (alternating current and direct current) as an adjunctive therapy to treating lumbosacral radiculopathy. Both types of electrical stimulation have been used in clinical practice for physical therapy, however direct current stimulation is much less common and there is less known about its impact on physical therapy outcomes. The aim of this project is to show the efficacy of a novel device, the Neubie direct current device, compared to traditional TENS unit in clinical physical therapy treatment of radiculopathy. Outcomes measured will include: pain intensity, functional status, neurological status, electrophysiological changes and patient satisfaction.

Eligibility criteria

Qualifiers

Must show evidence of lumbo-sacral radiculopathy as determined by EMG and straight leg raise test.

Must be able to attend weekly sessions for the 6-week period of the study (no extended travel)

Must be at least 18 years old.

Disqualifiers

Currently pregnant

Cardiac pacemaker

Active or recent cancer

Active or recent blood clots

Trial design

Treatments tested in this trial

  • Neubie Direct Current Electrical Stimulation Device
  • Transcutaneous Electrical Stimulation

Treatment groups

150 Participants
are divided into 2 treatment groups