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Anticipatory Postural Adjustments Characteristics in Patients with Chronic Non-Specific Low Back Pain and the Effects of Transcranial Direct Current Stimulation

The predictable postural control characteristics and the immediate effects of transcranial direct current stimulation in patients with CNLBP

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105328
Enrollment
Unknown
Registered
2025-07-02
Start date
2025-07-15
Completion date
Unknown
Last updated
2025-07-07

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

Intervention group 1:True stimulation - interval of 3~7 days - false stimulation Active transcranial direct current stimulation (tDCS) at 1.5 mA for 20 minutes targeting the supplementary motor area (

Sponsors

Beijing Sport University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1)Non-athletes aged 18 years or older; (2)Pain duration of 3 months or more; (3)An average pain intensity of 3 or higher on the Numeric Rating Scale (NRS) over the past week; (4)No treatment or rehabilitation intervention received for at least four weeks prior to enrollment; (5)Right-handed, with normal or corrected-to-normal vision; (6)Participants meet the safety criteria for anodal transcranial direct current stimulation (a-tDCS).

Exclusion criteria

Exclusion criteria: (1)Presence of radicular symptoms or a history of chronic pain in other body regions, or a history of current acute pain; (2)Specific low back pain due to causes such as tumor, infection, metabolic disease, rheumatoid arthritis, or fracture; (3)Extradural diseases (e.g., vascular or genitourinary system disorders); (4)History of any spinal surgery or hip/knee joint surgery; (5)Neurological disorders or a history of psychiatric illness; (6)Spinal deformities (e.g., spondylolisthesis, spondylolysis, or scoliosis); (7)Pregnancy.

Design outcomes

Primary

MeasureTime frame
Muscle onset latency;

Secondary

MeasureTime frame
Muscle activation level;Motion control test;Center of Pressure (CoP);

Countries

China

Contacts

Public ContactMengya Liu

Beijing Sport University

liumy66@163.com+86 132 8128 8660

Outcome results

None listed

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