Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT06984224

Pulsed Direct Current Electrical Stimulation for Treatment of Low Back Pain

The goal of this interventional clinical trail is to determine the efficacy of the use of the Neubie pulsed direct current electrical stimulation device for the treatment of participants experiencing mechanical low back pain. The main question it aims to answer is:

Does treatment with the Neubie improve symptoms and time to resolution of back pain compared to standard of care?

Researchers will compare a 12 session treatment physical therapy regimen using the Neubie to standard of care to see if there is a difference in symptom severity and time to resolution.

Participants will:

* Visit the clinic 2 times a week to undergo active physical therapy treatments with or without electrical stimulation from the Neubie. * Undergo testing and fill out surveys on evaluation and final session on quality of life, disability, pain, and spinal mobility.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Conditions

Back Pain, Low Back Pain Low Back Pain Neurologic Manifestations Pain Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

To determine the efficacy of direct current (DC) electrical stimulation (the Neubie device) on back pain, patients presenting with mechanical, non-radicular low back pain will enroll in a 4 to 6 week treatment regimen at EA Therapeutic Health. The first session will consist of an intake evaluation session that will include: Modified Oswestry Pain Scale, The Schober test for mobility, Heart Rate Variability, and Quality of Life Index. These tests will serve as baseline (and a within subject control) for the intervention.

Participants will then undergo a treatment protocol that incorporates either traditional physical therapy (PT) exercises (standard of care control) or PT exercises with the Neubie utilized concurrently (experimental group). Subjects will undergo an evaluation session prior to starting treatment that includes the Modified Oswestry Pain Scale, The Schober test for mobility, Heart Rate Variability, and Quality of Life Index.

The experimental group subjects will undergo 12 sessions of physical therapy over a 4 to 6-week period which include 45 min of various physical therapy exercises concurrently with the Neubie followed by a 15 minute passive Vagus nerve stimulation protocol with the Neubie.

Control group subjects will participate in a physical therapy protocol that includes manual therapy (e.g. trigger point release, mobilization of the sacroiliac (SI) joint and exercises for back strengthening and stretching. Experimental group subjects will participate in a physical therapy protocol that includes manual therapy (e.g. trigger point release, mobilization of the SI joint) and exercises for back strengthening and stretching in conjunction with Neubie DC e-stim. Both control and experimental groups will receive a customized Home Exercise Program with exercises to be performed at home 1 time a day.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Must show evidence of axial mechanical low back pain at least 3/10 on visual analog scale, without radiation to the lower limbs. Pain has to have been present for at least two weeks or diagnosed as chronic .
  • Normal lower limb strength
  • Able to attend twice weekly physical therapy visis for up to 6 weeks
  • 18 years of age, or older

Exclusion criteria

  • Currently pregnant
  • Cardiac pacemaker
  • Active or recently treated cancer
  • Active or recent blood clots
  • Epilepsy
  • Open wounds
  • History of lumbar spine fusion surgery
  • Radicular symptoms suggesting radiculopathy or spinal stenosis.

Treatment and study plan

Neubie Direct Current Stimulation Device

Device

Pulsed Direct Current Electrical Stimulation Device

Primary outcomes

  1. Modified Oswestry Disability Index

    Time frame: Pre-intervention

    MODIFIED OSWESTRY DISABILITY SCALE - Each question is scored from 0-5 (minimum to maximum). The point total from each section is summed and the then divided by the total number of questions answered and multiplied by 100 to create a percentage disability. The scores range from 0-100% with lower scores meaning less disability.

  2. Modified Oswestry Disability Index

    Time frame: 6 weeks

    MODIFIED OSWESTRY DISABILITY SCALE - Each question is scored from 0-5 (minimum to maximum). The point total from each section is summed and the then divided by the total number of questions answered and multiplied by 100 to create a percentage disability. The scores range from 0-100% with lower scores meaning less disability.

  3. Visual Analog Pain Scale

    Time frame: Pre-intervention

    The Visual Analog Scale (VAS) for measuring pain ranges from 0-10, with 0 representing "no pain" and 10 representing "worst pain imaginable".

  4. Visual Analog Pain Scale

    Time frame: 6 weeks

    The Visual Analog Scale (VAS) for measuring pain ranges from 0-10, with 0 representing "no pain" and 10 representing "worst pain imaginable".

  5. Schober Test

    Time frame: Pre-intervention

    Schober Test for Spinal Mobility

  6. Schober Test

    Time frame: 6 weeks

    Schober Test for Spinal Mobility

  7. Quality of Life Index

    Time frame: Pre-intervention

    Quality of Life Index Score has a range from 0 to 100. Lower values represent poorer quality of life, while higher values indicate better quality of life.

  8. Quality of Life Index

    Time frame: 6 weeks

    Quality of Life Index Score has a range from 0 to 100. Lower values represent poorer quality of life, while higher values indicate better quality of life.

  9. Heart Math HRV

    Time frame: Pre-intervention

    The Heart Math HRV system takes a reading of the participant's HRV. This is provided in a numerical value which will be used as the HRV "score".

  10. Heart Math HRV

    Time frame: 6 weeks

    The Heart Math HRV system takes a reading of the participant's HRV. This is provided in a numerical value which will be used as the HRV "score".

Study contacts

Contact information is provided by the study sponsor or research team.

Melanie Brennan

CONTACT

[email protected]

Ramona von Leden

CONTACT

[email protected]

5303832292

Sponsors and collaborators

Lead sponsor

NeuFit - Neurological Fitness and Education

Industry

Collaborators

  • EA Therapeutic Health
  • Mayo Clinic

Registry information

Official study title

Efficacy of Pulsed Direct Current Electrical Stimulation (Neubie) on Low Back Pain

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
May 22, 2025
Registry last updated
May 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.