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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