Chronic low back pain
Conditions
Interventions
Experimental group:Cerebellar tDCS (2mA,20min,3 times per week, four weeks) with core stability training
Control group:Cerebellar sham tDCS (2mA,20min,3 times per week, four weeks) with core stability training
Sponsors
The Fifth Affiliated Hospital of Guangzhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 55 Years
Inclusion criteria
Inclusion criteria: (1) Participants voluntarily enrolled in the study and provided written informed consent; (2) Aged 18–55 years; (3) Chronic low back pain (LBP) persisting for >3 months, with no analgesic medication use within the preceding two weeks; (4) No history of lumbar disc herniation, scoliosis, spinal trauma, or surgical interventions; (5) Absence of intracranial metallic implants, epilepsy, psychiatric disorders, or malignancies.
Exclusion criteria
Exclusion criteria: (1) Presence of lower limb numbness; (2) Suspected or confirmed pregnancy; (3) Patients deemed by the investigator to be ineligible for study participation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analogue Scale;Pain Catastrophizing Scale;Pain Self-Efficacy Questionnaire,PSEQ;RMDQ(Roland Morris Disability Questionnaire; | — |
Secondary
| Measure | Time frame |
|---|---|
| Anticipatory postural adjustment; | — |
Countries
China
Contacts
Public ContactMao Haian
The Fifth Affiliated Hospital of Guangzhou Medical University
Outcome results
None listed