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Multimodal EMG and neuroimaging study of tDCS synchronous hemiplegic upper limb FES on functional recovery after stroke

Multimodal EMG and neuroimaging study of tDCS synchronous hemiplegic upper limb FES on functional recovery after stroke

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058057
Enrollment
Unknown
Registered
2022-03-28
Start date
2021-10-01
Completion date
Unknown
Last updated
2023-12-03

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

Conditions

Stroke

Interventions

Group 1:tDCS+FES
Group 2:sham tDCS+FES
Group 3:tDCS+sham FES

Sponsors

SUN YAT-SEN MEMORIAL HOSPITAL, SUN YAT-SEN UNIVERSITY
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 40-80 years; 2. First cerebral infarction; 3. Patients with previous lacunar cerebral infarction without sequelae; 4. The diagnosis conforms to the diagnostic points of various cerebrovascular diseases adopted at the Fourth National Conference on Cerebrovascular Diseases in 1995; 5. Confirmed by head CT or MRI; 6. 3 months <=the onset time <=6 months, with upper limb dysfunction; 7. Brunnstrom grade of the affected upper limb stage III-V; 8. Informed consent signed by the patient himself or by his immediate family members.

Exclusion criteria

Exclusion criteria: 1. Inpatients with unconsciousness and MMSE evaluation indicating dementia, sensory aphasia or mental disorders, and unable to cooperate with examination and treatment; 2. Patients with serious primary diseases of the heart, liver, kidney and hematopoietic system; 3. Previous history of cognitive impairment, neuropsychiatry, drug abuse and alcoholism; 4. Stroke patients with major organ failure or critical condition, cancer and other diseases or states that affect the quality of life of patients more than the limb dysfunction after stroke; 5. Those who cannot complete the basic course of treatment and may have poor compliance (that is, can not adhere to the treatment) and difficult to follow the patients; 6. Patients with metal implants in upper limbs and intracranial.

Design outcomes

Primary

MeasureTime frame
Upper function;

Secondary

MeasureTime frame
MRI;Electrophysiology;Surface electromyography;

Countries

China

Contacts

Public ContactLiu Huihua

SUN YAT-SEN MEMORIAL HOSPITAL, SUN YAT-SEN UNIVERSITY

liuhuihua@mail.sysu.edu.cn+86 20 81332880

Outcome results

None listed

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