tDCS trial for musculoskeletal and spinal cord diseases
- Conditions
- Cervical spondylotic myelopathy, Cervical spondylotic amyotrophy, Lumbar spinal canal stenosis, RotaCervical spondylotic myelopathy, Cervical spondylotic amyotrophy, Lumbar spinal canal stenosis, Rotator cuff tear, Frozen shoulderC10.228.854, C26.761.340, C05.550.251
- Registration Number
- JPRN-jRCTs032180298
- Lead Sponsor
- Shitara Hitoshi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 160
1)Participants who can be obtained informed consent from themselves
2)Currently, taking no medical treatment for serious health reasons such as mental and neurological diseases.
3)Health subjects or Patients with cervical spondylotic myelopathy, cervical spondylotic amyotrophy, lumbar spinal canal stenosis, rotator cuff tear, or frozen shoulder
4)Dominant hand or foot is the right
5)No contraindication on the implementation of transcranial magnetic stimulation (TMS) or tDCS
1)Patients with complication of more than one disease which is cervical spondylotic myelopathy, cervical spondylotic amyotrophy, lumbar spinal canal stenosis, rotator cuff tear, or frozen shoulder
2)Patients with obvious resting pain
3)Suspected women who are pregnancy
4)Complete paralysis
5)Participants who have any contraindications on the implementation of TMS or TMS
6)Participants who have any contraindications for undergoing an MRI scan
7)Participants who are judged unsuitable subjects by a doctor
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method