Skip to content

To investigate the clinical efficacy and neural mechanism of HD-tDCS in somatosensory cortex combined with core stability training in patients with chronic low back pain

To investigate the clinical efficacy and neural mechanism of HD-tDCS in somatosensory cortex combined with core stability training in patients with chronic low back pain

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076620
Enrollment
Unknown
Registered
2023-10-13
Start date
2023-11-01
Completion date
Unknown
Last updated
2023-10-16

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

A Group:Anodal High- definition transcranial direct current stimulation targeting at primary somatosensory cortex and Core stability exercise
B group:Cathodal High- definition transcranial direct current stimulation targeting at S1 and Core stability exercise
C group:Sham stimulation targeting at primary somatosensory cortex and Core stability exercise

Sponsors

The first affiliated hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. medical diagnosis of non-specific LBP with pain and symptoms persisting for more than 3 months and visual analogue scale (VAS)>3 cm. 2. aged 18–40 years and without history of other diseases. Participants were excluded if they had any of the followings: 1) outside the range of age, 2) pregnant, 3) acute LBP or sub-acute LBP. 3. chronic LBP of traumatic or structural origin, LBP with neurological symptoms or pain radiation in the lower leg(s). 4. previous back surgery, spinal tumors or infections, or neurological and/or musculoskeletal disorders unrelated to LBP. 5.No history of non-steroidal anti-inflammatory drugs and other drugs in the past half a year.

Exclusion criteria

Exclusion criteria: Subjects who did not meet the above inclusion criteria or were pregnant.

Design outcomes

Primary

MeasureTime frame
Visual Analog Score, VAS;westry Disability Index, ODI;Pain Catastrophizing Scale, PCS;

Secondary

MeasureTime frame
Thickness of TrA and MF;Ability of postural control;Onset time, MF and MFV;Beta;Pearson correction coefficient;Roland Morris Disability Questionnaire, RMDQ;

Countries

China

Contacts

Public ContactHongjiang Wang

The first affiliated hospital, Sun Yat-sen University

wanghj73@mail.sysu.edu.cn+86 156 0239 2369

Outcome results

None listed

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