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The effect of eight weeks of spinal mobilization apparatus on pain and muscle fatigue in patients with non-specific low back pain

The effect of Spinal mobilization apparatus on pain and muscle fatigue in patients with non-specific Low back pain

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042333
Enrollment
Unknown
Registered
2021-01-19
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-04-19

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

Conditions

non-specific low back pain

Interventions

intervention group:Spinal joint loosening apparatus + sling exercise training
control group:sling exercise training

Sponsors

Ningbo College of Health Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Medical history: Most of the patients had a history of acute lumbar sprain and chronic low back pain; (2) Symptoms: The patient's lower back pain is obviously diffuse and has unclear location. It is often accompanied by hip discomfort and pain in the back of the thigh, but the range is generally not more than the knee joint; (3) Signs: Increased muscle tension in the lower back, bands and nodules can be reached in the muscles, accompanied by low back pain. The physiological radian of waist decreases or even disappears, and the spine process can be touched, and the range of waist movement is obviously limited. (4) Imaging examination: no obvious abnormalities were found, part of the spine has rotational scoliosis, and the pelvis is not ascending or equal width. Physiological radian change, lumbar vertebra bone hyperplasia. (5) No relevant treatment has been given in the past two weeks; (6) Patients voluntarily participate in this study, agree and sign informed consent; (7) Aged between 18 and 65 years. If the above conditions are met, it can be included in this study.

Exclusion criteria

Exclusion criteria: (1) Fail to cooperate with examination and treatment; (2) Receive other treatments during the treatment; (3) Imaging findings of root compression, accompanied by symptoms of corresponding innervated muscles and sensory areas; (4) Patients with tumor, mandatory spondylitis, tuberculosis, fracture, etc. after laboratory examination shall be excluded; (5) Critically ill patients: recent unstable blood pressure control and women's pregnancy; Patients with abnormal coagulation function; (6) Severe skin injury or skin disease in the manipulation part; Any one of the above items shall be excluded.

Design outcomes

Primary

MeasureTime frame
JOA scale;

Secondary

MeasureTime frame
visual analogue scale;muscle thickness(Transverse abdominis, multifissure and erector spinalis);core muscle group endurance test;Intra-abdominal pressure;Surface electromyography;range of motion;Sf-36 Self-rating Health Scale;

Countries

China

Contacts

Public ContactYang Faming

Ningbo College of Health Sciences

64577698@qq.com+86 17815919753

Outcome results

None listed

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