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tDCS trial for musculoskeletal and spinal cord diseases

Not Applicable
Recruiting
Conditions
Cervical spondylotic myelopathy, Cervical spondylotic amyotrophy, Lumbar spinal canal stenosis, Rota
Cervical spondylotic myelopathy, Cervical spondylotic amyotrophy, Lumbar spinal canal stenosis, Rotator cuff tear, Frozen shoulder
C10.228.854, 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
Inclusion Criteria

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

Exclusion Criteria

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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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