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High-Definition Transcranial Direct Current Stimulation Combined with Attentional Bias Modification Training on Alpha Oscillations in Chronic Low Back Pain

High-Definition Transcranial Direct Current Stimulation Combined with Attentional Bias Modification Training on Alpha Oscillations in Chronic Low Back Pain

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066247
Enrollment
Unknown
Registered
2022-11-29
Start date
2022-12-01
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low back pain

Interventions

group1:Real HD-tDCS + ABM
group2:sham HD-tDCS + ABM

Sponsors

The Sixth Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
22 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Being right-handed; 2) aged 18-65 years, with a history of chronic low back pain for more than 3 months, and a mean NRS score of rest pain greater than 3 on a scale of 0-10 in the past week; 3) BDI score, non-depressed patients; 4) have not participated in psychological experiments before; 5) body mass index (BMI) should be in the normal range: 18.5 ± 27kg/m2; 6) pain-modifying medications (including antipyretics and sleeping pills) should not be taken; Female candidates should be in the middle and late follicular phase; 7) Patients with a score less than 24 on the Mini-Mental State Examination (MMSE) were excluded; 8) have normal or corrected vision and normal color vision.

Exclusion criteria

Exclusion criteria: 1) Body index > 30 kg/m2; 2) with metal and electronic implants; Known intracranial tumors and a history of craniocerebral injury; 3) intake of opioid analgesics , tetracyclic antidepressants, antiviral drugs and antipsychotics; The use of narcotic analgesics was tested in the first two weeks; Use of non-narcotic analgesics (e.g., NSAIDs) 24 hours before testing; 4) frequent headache or tinnitus and a history of alcohol or drug abuse; Confirmation or suspicion of pregnancy and lactation; 5) include evidence of spinal cord defects, any history of back/brain surgery; 6) diagnosed acute or chronic mental illness or other mental illness; Severe neurological disorders; History of epilepsy, family history of epilepsy; A 15-minute history of loss of consciousness; 7) pregnancy, any open wounds on the scalp and/or face; 8) hearing or vision impairment; Illiterate; 9) have any contraindications to tDCS; 10) drug dependence/abuse or presence of a degenerative disease (e.g., Alzheimer's disease); 11) consume > 8 units of caffeine per day (maximum one cup of caffeine on the test day); Smokers daily > 5 pieces; 12) severe depression with a score greater than 35 on the Beck Depression Inventory (BDI).

Design outcomes

Primary

MeasureTime frame
Alpha Oscillations;

Secondary

MeasureTime frame
Pain-threshold;

Countries

China

Contacts

Public ContactYuling Wang

The Sixth Affiliated Hospital of Sun Yat-sen University

Wangyul@mail.sysu.edu.cn+86 13054445587

Outcome results

None listed

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