Cognitive Dysfunction Clinical Trial
Official title:
A Multi-center RCT Study on the Efficacy and Mechanism of Multi-channel tDCS in Rehabilitation of Cognitive Function After Stroke
This clinical RCT study intends to combined different forms of multi-channel tDCS with the routine cognitive training process to treat patients with post-stroke cognitive dysfunction. The therapeutic effects among single-channel tDCS group, multi-channel tDCS and pseudo-multichannel tDCS group will be compared. Brain magnetic resonance mechanism research will also be included to reveal the possible mechanism of multi-channel tDCS technology for PSCI brain network. Thus, the efficacy and mechanism of multi-channel tDCS in post-stroke cognitive function rehabilitation will be researched both in the clinical and basic levels.
| Status | Recruiting |
| Enrollment | 180 |
| Est. completion date | December 2023 |
| Est. primary completion date | March 2023 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 60 Years |
| Eligibility | Inclusion Criteria: - 18-60 year-old - diagnosed cerebral apoplexy, meeting the diagnostic criteria of ICD-10 - cognitive function, perceptual function decline after stroke - first onset and duration of 3-12 months - right-handed - MMSE =25 - MoCA =25 - sign informed consent voluntarily and comply with the study plan Exclusion Criteria: - NIHSS =21 points - MoCA =18, or DRS-2 = 124, or CES-D = 16 - taking drugs that affect central nervous activity, such as nerve antagonists - specific contraindication, such as electrode patch allergy, local skin injury or - - - - inflammation, and hyperalgesia in stimulated areas - patients use implantable electronic devices (such as cardiac pacemakers) or have - metal implants such as stents that affect MRI examination - patients with a previous history of epilepsy, mental illness or skull injury - patients with dementia or obvious cognitive dysfunction before stroke - patients with aphasia or dysarthria and cannot complete the scale evaluation - pregnancy |
| Country | Name | City | State |
|---|---|---|---|
| China | Southwest Hospital | Chongqing | |
| China | Rainbowfish Rehabilitation Nursing Care | Hangzhou | Zhejiang |
| China | SAHZhejiangU | Hangzhou | Zhejiang |
| China | Zhejiang Provincial People's Hospital | Hangzhou | Zhejiang |
| Lead Sponsor | Collaborator |
|---|---|
| Second Affiliated Hospital, School of Medicine, Zhejiang University |
China,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | MMSE | Mini-mental State Examination | Change from Baseline MMSE at 2 weeks and 3 months after intervention | |
| Primary | MoCA | Montreal Cognitive Assessment | Change from Baseline MoCA at 2 weeks and 3 months after intervention | |
| Primary | AVLT | The Auditory-Verbal Learning Test | Change from Baseline AVLT at 2 weeks and 3 months after intervention | |
| Primary | WAIS-DST | WAIS Digit Symbol Test | Change from Baseline WAIS-DST at 2 weeks and 3 months after intervention | |
| Secondary | DEX | Dysexecutive Ques-tionnaire | Change from Baseline DEX at 2 weeks and 3 months after intervention | |
| Secondary | GNAT | Go/No-go Association Task | Change from Baseline GNAT at 2 weeks and 3 months after intervention |
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