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Cupping exercise therapy for patients with chronic non-specific low back pain: a randomized controlled trial

Cupping exercise therapy for patients with chronic non-specific low back pain: a randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082992
Enrollment
Unknown
Registered
2024-04-12
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Chronic Non-specific Low Back Pain

Interventions

Cupping + Walking Exercise Group:With the patient in the prone position, the therapist performs symmetrical rows of canisters centered along the patients lumbosacral bladder meridian (bilaterally para
Health Education Group:Health Education

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: ? Based on the diagnostic criteria for chronic non-specific low back pain provided by the American Physical Therapy Association (APTA): (1) Persistent pain in the posterior trunk, from the lower border of the 12th rib to the inferior border of the gluteus maximus, with or without radiating pain in the outer aspect of the thigh (pain not extending below the level of the knee joint); (2) Local tenderness or muscle spasms upon physical examination; (3) Apart from imaging findings such as vertebral and facet joint morphological changes, no other positive findings are present; (4) Duration of overall pain > 12 weeks. ? Age: 18-60 years; gender not limited; BMI: 18-24 kg/m2. ? Visual Analogue Scale (VAS) score: 3-8. ? No history of lumbar surgery or standardized non-surgical treatment. ? No analgesic medication taken in the 2 weeks prior to enrollment. ? Signed informed consent form.

Exclusion criteria

Exclusion criteria: ? History of vertebral fractures or spinal surgery; ? Diagnosed with ankylosing spondylitis, scoliosis, spondylolisthesis, or isthmic spondylolysis; ? Presence of concurrent conditions such as spinal tuberculosis, fractures, tumors, or other pathological lesions in the lumbar region; ? Presence of other severe diseases, such as cancer, stroke, or mental disorders; ? Pregnant or lactating women. ? Presence of contraindications for cupping therapy, such as renal dysfunction, hepatic cardiac dysfunction, the presence of a pacemaker, pregnancy, or skin diseases in the treatment area.

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale (VAS);Lumbar Range of Motion;

Secondary

MeasureTime frame
Japanese Orthopaedic Association;Oswestry Disability Index;Thickness of the thoracolumbar fascia;SF-36 scale;Lumbar multifidus muscle cross-sectional area;Lumbar erector spinae muscle cross-sectional area;lumbar erector spinae muscle elasticity and lumbar multifidus muscle elasticity;

Countries

China

Contacts

Public ContactDebiao Yu

Fujian Provincial Hospital

405528346@qq.com+86 159 8022 5823

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026