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Effects of TDCS combined FES on upper limb function with severe chronic stroke patients

Effects of TDCS combined FES on upper limb function with severe chronic stroke patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ICR-15006108
Enrollment
Unknown
Registered
2015-03-15
Start date
2015-03-19
Completion date
Unknown
Last updated
2017-07-03

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

Conditions

upper limb fucntion impairment after stroke

Interventions

FES+TDCS Group:TDCS combine FES therapy
FES+sham TDCS group:sham TDCS+FES therapy

Sponsors

Shanghai Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Age between 35 and 70 years; (2) Cerebral hemorrhage or cerebral infraction for the first time; (3) No sequelae after lacunar cerebral infraction; (4) Satisfying the cerebrovascular disease diagnostic criteria defined by The 4th National Conference on Cerebrovascular Disease, 1995; (5) Confirmed by head CT or MRI; (6) Time since stroke of 6 months at least an ipsilateral arm Brunnstrom recovery at stages 0-3; (7) No metals implanted; (8) Conscious and able to communicate; (9) No peripheral neuropathy with upper limb; (10) Signed informed consent himself (herself) or his (her) immediate family member.

Exclusion criteria

Exclusion criteria: (1) Not satisfying the cerebrovascular disease diagnostic criteria defined by The Fourth National Conference on Cerebrovascular Disease, 1995; (2) Not first cerebral hemorrhage or cerebral infraction, lacunar infraction with squelae; (3) Unconsciousness,or with sensory aphasia or mental disorders, cannot coordinate examination and treatment; (4) With serious illnesses, such as heart, liver or kidney diseases, or serious coagulation disorders; (5) With a history of cognitive disorder, neuropsychiatric disorder, drug or alcohol abuse; (6) With organ failure, carcinoma or fatal stroke that seriously affect life quality more than hand dysfunction; (7) Time since stroke less than 6 months; (8) Cannot complete basic course, cannot persist treatment, or be difficult to follow-up; (9) With upper limb metal implants or skull defect; (10) Claustrophobia, unable to accept the fMRI examination.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer scale of upper limb;Wolf motor function test;modified Ashworth scale;fMRI;TMS;SEMG;WHOQOL-BREF Scale;

Countries

China

Contacts

Public ContactDingguo Zhang
dgzhang@sjtu.edu.cn+86 18918963613

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 24, 2026