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Comparative study of different tDCS stimulation on brain function and upper limb rehabilitation in stroke patients

Comparative study of different tDCS stimulation on brain function and upper limb rehabilitation in stroke patients

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082837
Enrollment
Unknown
Registered
2024-04-09
Start date
2023-11-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

stroke dysphagia

Interventions

bi-tDCS group:The patient was treated with anode tDCS on the basis of routine rehabilitation training. Sponge electrode 5 cm × 7 cm. According to the international electroencephalography 10-20 system
a-tDCS group:The patient was treated with anode tDCS on the basis of routine rehabilitation training. Sponge electrode 5 cm × 7 cm. According to the electrode placement method of the international EEG
c-tDCS group:The patient was treated with cathode tDCS on the basis of routine rehabilitation training. Sponge electrode 5 cm × 7 cm. According to the electrode placement method of the international E
sham-tDCS group:Patients were randomized to receive sham stimulation of tDCS in the unaffected or lesional hemisphere, with the same electrode placement position and treatment parameters as the above

Sponsors

Zibo Central Hospital of Shandong Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria of ischemic stroke in the Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke; (2) First onset, unilateral lesions, paralysis of one limb; (3) Age =18 years old (4) Duration of disease =6 months (5) hemiplegic side Brunnstrom stage upper limb stage I-V; (6) Simple Mental State Examination Scale (MMSE) score =24 points (primary education =20 points, illiteracy =17 points) (7) Patients and their families voluntarily participate and sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Progressive stroke; (2) Head skin infection or damage; (3) Have a history of epilepsy and use of antiepileptic drugs; (4) Carrying an implantable electronic device (such as a pacemaker); (5) Take antidepressants, anxiety and other neurologic drugs

Design outcomes

Primary

MeasureTime frame
delta/alpha power ratio,DAR;Brain symmetry index,BSI;Fugl-Meyer Assessment-Upper Extremity,FMA-UE;

Secondary

MeasureTime frame
Wolf Motor Function Test,WMFT;Simple Test for Evaluating Hand Function,STEF;Functional Independence Measure,FIM;

Countries

China

Contacts

Public ContactHoubing;Zhao hongfei

School of Nursing and Rehabilitation, Caofeidian Campus, North China University of Science and Technology, Tangshan City, Hebei Province Zibo Central Hospital of Shandong Province

houbing220@163.com+86 186 3094 8701

Outcome results

None listed

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