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Effect of transcutaneous spinal cord direct current stimulation combined with exercise therapy on chronic low back pain

Effect of transcutaneous spinal cord direct current stimulation combined with exercise therapy on chronic low back pain

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078852
Enrollment
Unknown
Registered
2023-12-20
Start date
2023-12-22
Completion date
Unknown
Last updated
2024-01-08

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

tsDCS group:(1) tsDCS treatment, 20 minutes each time, 5 times a week for 4 consecutive weeks
(2) Exercise therapy, including activation training, static stability training, dynamic stability training and activation training, 30 minutes each time, 5 times a week for 4 consecutive weeks.
sham group:(1) sham stimulation, 20 minutes each time, 5 times a week for 4 consecutive weeks

Sponsors

Rehabilitation Department,First Affiliated Hospital of Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Age 18-60 years old, gender is not limited; (2) low back pain lasting at least 12 weeks, at least once a week; (3) Visual analog scale (VAS), 3=VAS < 7; (4) Oswestry Disability Index (ODI), ODI=12%;

Exclusion criteria

Exclusion criteria: (1) Specific low back pain caused by definite pathological changes in the lumbar spine, such as discogenic low back pain, ankylosing spondylitis, spinal tumors, visceral diseases, and spinal trauma; (2) Acute or chronic musculoskeletal system pain in other parts of the body; (3) Skin damage at any treatment site (broken or infected skin); (4) Use of implantable electronic devices (such as pacemakers); (5) Highly conductive metals in any part of the body (e.g. electrical/metal implants, internal fixation devices, etc.); (6) History of seizures in the past 36 months; (7) Use of painkillers, psychotropic drugs or alcohol abuse history; (8) Women who are menstruating, pregnant or preparing for pregnancy; (9) Those who do not want to sign the informed consent.

Design outcomes

Primary

MeasureTime frame
pain;

Secondary

MeasureTime frame
pain;Muscle strength and Activation;Balance and Proprioception;Magnetic resonance imaging;Patient-reported outcomes;

Countries

China

Contacts

Public ContactJingming Hou

The First Affiliated Hospital of Military Medical University

hjmkfk@163.com+86 177 2356 2203

Outcome results

None listed

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