Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07368920

Transcutaneous Electrical Nerve Stimulation (TENS) for the Treatment of Low Back Pain (LBP) in Adults

Led by Xijing Hospital · Updated on 2026-03-20

40

Participants Needed

1

Research Sites

152 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to assess the effects and safety of transcutaneous electrical nerve stimulation (TENS) in adults with myofascial low back pain. Eligible participants will receive TENS treatment 5 times per week for 4 weeks. Pain intensity and functional outcomes will be assessed at baseline and weekly during the 4-week treatment period, and adverse events will be recorded.

CONDITIONS

Official Title

Transcutaneous Electrical Nerve Stimulation (TENS) for the Treatment of Low Back Pain (LBP) in Adults

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 65 years
  • Diagnosis of myofascial low back pain characterized by localized pain with a palpable taut band, a specific trigger point with referred pain or sensory changes, and an identifiable tender spot
  • Mild baseline pain intensity (VAS score less than 4 on a 0-10 scale)
  • Symptoms present for more than 1 month
  • Able to understand study procedures and cooperate well
  • Provided written informed consent
Not Eligible

You will not qualify if you...

  • Low back pain caused by other conditions such as lumbar disc herniation, spinal stenosis, ankylosing spondylitis, spinal tumor, tuberculosis, or infection
  • Received physical therapy, interventional procedures, or medication affecting pain or function within 4 weeks before enrollment
  • Presence of systemic disease or organ dysfunction
  • Skin or soft tissue breakdown or infection near the treatment area
  • Use of sedatives or opioid painkillers within 6 months before enrollment or currently receiving treatments that may affect outcomes
  • Severe psychiatric disorders or inability to cooperate with study procedures
  • Pregnant or breastfeeding women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Xjing hospital

Xi'an, Shaanxi, China, 710032

Actively Recruiting

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Research Team

B

Bo Gao MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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