Stroke
Conditions
Interventions
Experimental group:cerebellar tDCS + upper limb training
Control group:cerebellar sham tDCS + upperlimb training
Sponsors
The Fifth Affiliated Hospital of Guangzhou Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.First-ever supratentorial stroke or prior supratentorial stroke without residual hand dysfunction; 2.Post-stroke duration: 2 weeks to 10 years; 3.Observable lesion confirmed by MRI or CT imaging; 4.Ability to maintain a seated position with backrest support for >=40 minutes; 5.Absence of severe cognitive impairment (Mini-Mental State Examination [MMSE] score >21) and capacity to follow verbal commands.
Exclusion criteria
Exclusion criteria: 1.Pregnant or lactating patients; 2.Participation in drug or medical device clinical trials within the preceding three months; 3.Patients deemed ineligible for study participation by the investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Upperlimb Fugl-Meyer scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| mean HbO concentration ;lateralization Index;networ connectivity; | — |
Countries
China
Contacts
Public ContactMao Haian
The Fifth Affiliated Hospital of Guangzhou Medical University
Outcome results
None listed