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A Randomized Controlled Clinical Study on the Improvement of Chronic Low Back Pain Symptoms Using an Extracorporeal Shortwave Diathermy Device

A Randomized Controlled Clinical Study on the Improvement of Chronic Low Back Pain Symptoms Using an Extracorporeal Shortwave Diathermy Device

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125954
Enrollment
Unknown
Registered
2026-06-01
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Back pain

Interventions

Intervention group (extracorporeal shortwave diathermy + conventional rehabilitation):Extracorporeal shortwave diathermy
Control group (sham irradiation conventional rehabilitation)
:Rehabilitation exercise

Sponsors

Wuhan Orthopaedics Hospital of Integrated Traditional Chinese and Western Medicine The Affiliated Hospital of Wuhan Sports University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 65 years, male or female; 2. Meet the diagnostic criteria for chronic low back pain, with a disease duration of more than 3 months. 3. Average pain Visual Analog Scale (VAS) score >= 4 points within the past week; 4.Voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Presence of definite specific spinal pathological changes (e.g., spinal tumor, tuberculosis, fracture, ankylosing spondylitis, etc.); 2. Accompanied by severe lumbar disc herniation with obvious nerve root compression symptoms or clear surgical indications; 3. Implanted cardiac pacemaker, neurostimulator, or presence of metal implants in the treatment area; 4. Pregnant or lactating women; 5.Concurrent severe primary diseases of the cardiovascular, cerebrovascular, hepatic, renal, or hematopoietic systems, or cognitive and mental disorders that preclude cooperation with scale assessments; 6. Presence of an intrauterine device (IUD); 7. Patients with tuberculosis, active acute inflammation (e.g., acute suppurative inflammation), bleeding disorders, or bleeding tendencies; 8.Female menstrual period; 9.Thermoregulatory disorders or sensory disorders; 10. Postoperative wound not healed; 11.Patients with severe cardiovascular or cerebrovascular diseases; 12.Patients with calculi (stones).

Design outcomes

Primary

MeasureTime frame
Pain Visual Analog Scale (VAS) score;

Secondary

MeasureTime frame
Record of rescue oral analgesic use during the trial;SF-36 Quality of Life Scale Score;Single-leg stance time (or Single-leg standing time);apanese Orthopaedic Association (JOA) Score;Oswestry Disability Index (ODI) score;finger to floor distance,FFD;Assessment of cross-sectional area and thickness change rate of the multifidus muscle using a musculoskeletal ultrasound device;

Countries

China

Contacts

Public ContactChen Wang

Wuhan Orthopaedics Hospital of Integrated Traditional Chinese and Western Medicine The Affiliated Hospital of Wuhan Sports University

408414296@qq.com+86 27 86643885

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026