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Electrophysiologic characteristics of patients with chronic nonspecific low back pain in sit-to-stand tasks and the effect of manipulative therapy on such patients

Electrophysiologic characteristics of patients with chronic nonspecific low back pain in sit-to-stand tasks and the effect of manipulative therapy on such patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075141
Enrollment
Unknown
Registered
2023-08-26
Start date
2023-08-26
Completion date
Unknown
Last updated
2023-08-28

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

CNLBPgroup:Maitland joint mobilization technique

Sponsors

chengdu sport university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for CNLBP group ? Duration of low back pain =3 months; ? Average pain intensity of 3 or higher in the past week on a 0-10 numerical rating scale; ? No treatment and rehabilitation intervention for at least four weeks prior to enrollment; ? Non-athletes aged 18 or older; ? Right-handed with normal or corrected-to-normal vision. Inclusion criteria for the Con group ? Subjects who have neither experienced low back pain nor sustained low back pain for more than three days in the past year; ? Non-athletes aged 18 or above; ? Right-handed with normal or corrected-to-normal visual acuity.

Exclusion criteria

Exclusion criteria: Exclusion Criteria for CNLBP Group/Con Group ? Low back pain with radicular symptoms, or accompanied by a history of chronic pain in other parts of the body or a history of current acute pain. ? Lower back pain with radicular symptoms or history of chronic pain in other parts of the body or current acute pain; ? Atopic lower back pain (tumor, infection, metabolic disease, rheumatoid arthritis, fracture); (iii) Extraspinal disorders (e.g., vascular, genitourinary); ? History of any spinal surgery or hip or knee surgery; ? Neurologic disease, history of psychiatric illness; ? Spinal deformity (spondylolisthesis, isthmic bifida, or scoliosis); ? Pregnancy; ? Analgesic, anxiolytic/sedative or antidepressant medications taken in the past month; ? Consumption of any caffeine-containing food or beverage within 24 hours prior to the day of the test.

Design outcomes

Primary

MeasureTime frame
electromyography;

Secondary

MeasureTime frame
pressure pain threshold;lumbar spine mobility;visual analogue scale;

Countries

China

Contacts

Public ContactMinjia Wang

Chengdu Sport University

wangminjia@cdsu.edu.cn+86 133 4096 1727

Outcome results

None listed

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