A Study on the Efficacy of Dual-Carrier-Frequency Transcranial Alternating Current Stimulation Modulating the Hippocampus for the Treatment of Chronic Non-Specific Low Back Pain

NCT ID
NCT07832188
Registry status
Recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Qilu Hospital of Shandong University
Conditions
Chronic Pain

Overview

ClinicalTrials.gov lists this study as Recruiting.

Enrollment: 60 participants (Estimated).

What is being studied

  • Intervention: Behavioral Disciplines and Activities
  • Intervention: Convulsive Therapy
  • Device: Dual-carrier-frequency transcranial alternating current stimulation
  • Intervention: Electric Stimulation Therapy
  • Intervention: Electroshock
  • Intervention: Psychiatric Somatic Therapies
  • Intervention: Psychological Techniques
  • Intervention: Therapeutics
  • Intervention: Transcranial Direct Current Stimulation
  • Device: Transcranial electrical stimulation (tES)

Who may be eligible

Ages
18 Years to 80 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: 1. Age between 18 and 80 years; 2. Meets the diagnostic criteria for non-specific low back pain as specified in the Chinese Clinical Guidelines for the Diagnosis and Treatment of Non-specific Low Back Pain (2022) ; 3. Diagnosed with chronic non-specific low back pain within the past 3 months, or pain located between T12 and the gluteal fold for at least half of the days within the past 6 months; 4. VAS score ≥ 3 (Visual Analogue Scale, 0-10); 5. Mechanical pain induced by posture, activity, and movement (e.g., flexion and functional movement tasks); 6. Voluntarily agrees to participate in this study and has signed the informed consent form. Exclusion Criteria: 1. Clear etiology of specific low back pain, such as vertebral fracture, severe spinal cord/nerve root compression symptoms (progressive neurological deficit), spinal infection, tumor, ankylosing spondylitis, etc.; 2. Prior major lumbar surgery or implants (e.g., internal fixation, spinal cord stimulation devices, etc.), or recent (within 3 months) invasive analgesic treatments such as nerve blocks or radiofrequency ablation; 3. Contraindications to MEG or MRI, including the presence of ferromagnetic metal implants in the body (e.g., cardiac pacemakers, hearing aids, carotid artery stents, etc.), claustrophobia that precludes MEG examination, or failed MEG acquisition; 4. History of severe cardiovascular disease, epilepsy, or other conditions that contraindicate electrical stimulation; 5. Pregnancy or lactation; 6. Cognitive impairment, psychiatric disorders, or other conditions that prevent understanding or compliance with the study procedures; 7. Rheumatic diseases, connective tissue diseases, or diabetes.

Study locations

1 study location is listed.

Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.

Countries: China

  • Shandong, China: 1

Sample of listed locations

  • Qilu hospital, Jinan, Shangdong — Jinan, Shandong, 250000, China — Recruiting

Study details

Start date
July 3, 2026
Primary completion date
September 24, 2029
Completion date
September 24, 2029
First posted
September 21, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07832188
Registry last updated
September 21, 2026
QualifiedStudies registry data refreshed
September 28, 2026
QualifiedStudies record fetched
September 28, 2026

View NCT07832188 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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