Effect of Lumbar-pelvic rhythmic training combined with ADIM on chronic nonspecific low back pain

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300074305

Enrollment

Unknown

Registered

2023-08-03

Start date

2023-08-14

Completion date

Unknown

Last updated

2023-08-07

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

Conditions

Chronic low back pain

Interventions

Intervention Group 1:abdominal drawing-in maneuver(ADIM)

Intervention Group 2:Lumbar-pelvic rhythmic training

Intervention Group 2:ADIM combined with Lumbar-pelvic rhythmic training

Control Group:Health and Physical Education

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Age > 18 years old; (2) chronic lower back pain lasting for more than three months; (3) Imaging examination showed no abnormality (4) No symptoms of lower extremity radiation pain or nerve root compression (5) Pain intensity on the visual analog scale (VAS) was between 3 and 8; (6) signs or symptoms of cardiovascular, pulmonary and/or metabolic diseases; (7) had at least 4 hours of sedentary work per day, had a sedentary lifestyle, and had no regular exercise in the past 3 months; (8) It is confirmed that they have not participated in similar experimental studies or exercise interventions in the past; (9) no history of smoking, anaemia or other cardiovascular diseases

Exclusion criteria

Exclusion criteria: (1) less than 6 months after lumbar, lower limb or abdominal surgery; (2)Rheumatic and inflammatory diseases (e.g. Rheumatoid Arthritis, ankylosing spondylitis, psoriatic arthritis, lupus erythematosus, Scheuermann disease) ; (3) mental illness and cognitive impairment; (4) progressive neurological disorder (e.g. multiple sclerosis, Parkinson's disease, motor neuron disease) ; (5) musculoskeletal system diseases, such as fracture, dislocation, structural abnormality, etc. (6) severe scoliosis; (7) history of vestibular and hearing impairment, hearing abnormality; (8) BMI =27.5; (9) pregnancy, malignant tumor, acute trauma, spinal cord compression, cauda equina syndrome, severe heart, lung, liver and kidney dysfunction;

Design outcomes

Primary

Measure	Time frame
Visual Analogue Scale(VAS);Transverse abdominis muscle thickness;	—

Secondary

Measure	Time frame
muscle area of multifarious ;Sorensen test;curl-up test;Side Bridge;Degree of muscle activation;Roland-Morris Disability Questionnaire(RMDQ);The Fear-avoidance Beliefs Questionnaire(FABQ);SF-36;	—

Countries

China

Contacts

Public ContactLiu Wei

Beijing Sport University

lwyx1998812@163.com+86 188 0147 9581

Outcome results

None listed

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