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Cortical activation patterns in response to peripheral stimulation and during exercise were compared between patients with chronic low back pain and healthy individuals by fNIRS

Cortical activation patterns in response to peripheral stimulation and during exercise were compared between patients with chronic low back pain and healthy individuals by fNIRS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500098495
Enrollment
Unknown
Registered
2025-03-10
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-17

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

Chronic low back pain gruop:None
Health control gruop:None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1)CLBP group: a. Aged >=18 years; b. Numerical Pain Rating Scale (NPRS) score >=3; c. Persistent low back pain lasting more than 3 months; d. Signed informed consent. 2)Healthy control group (HC group): a. Aged >=18 years; b. No acute or recurrent low back pain in the past six months, no history of chronic pain; c. Demographic characteristics (age, gender, BMI) matched 1:1 with the CLBP group; d. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1)Low back pain caused by specific pathologies, such as diagnosed or known conditions like arthritis, tumors, neurological diseases, fractures, herniated discs, ankylosing spondylitis, or rheumatism. 2)Diagnosed with or having any condition that may cause motor impairment, such as vestibular disorders. 3)Having a mental illness, such as depression or schizophrenia. 4)Pregnant or with a history of chronic pain. 5)Any degree of injury to the skin around the lower back area. 6)Taking painkillers or psychiatric medications within 24 hours prior to the test. 7)Receiving treatments that affect the central nervous system, such as TMS or iTBS, within 48 hours before the test.

Design outcomes

Primary

MeasureTime frame
The average change in oxygenated hemoglobin concentration in each brain region of interest compared to baseline.;The functional connectivity of each brain region of interest during the task;The electrical pain threshold on both sides of the L5 spinous process;

Secondary

MeasureTime frame
The Oswestry Disability Index;Numeric Pain Rating Scale;Chinese Version of Fear-Avoidance Belief Questionnaire;

Countries

China

Contacts

Public ContactLin Yang

West China Hospital, Sichuan University

Green.yanglin@scu.edu.cn+86 177 0811 2611

Outcome results

None listed

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