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