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International Cooperation Study on Rehabilitation Program of Cognitive Dysfunction After Stroke

International Cooperation Study on Rehabilitation Program of Cognitive Dysfunction After Stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003704
Enrollment
Unknown
Registered
2014-09-21
Start date
2013-08-03
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

stroke

Interventions

acupuncture group:basic treatment +acupuncture
RehaCom training group:basic treatment +RehaCom training
acupuncture & RehaCom group:basic treatment +acupuncture + RehaCom training

Sponsors

Fujian University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years old; 2. Diagnosed with stroke according to the criteria of 'Diagnostic Criteria for All Kinds of Cerebrovascular Disease'(made by the fourth national academic conference on cerebrovascular disease,1995), and confirmed by CT or MRI; 3. According to the Mini-Mental Status Examination(MMSE) screening: illiterate (uneducated) group 6 years) group<=24points; 4. The cognitive impairment must occur after stroke and to rule out other causes; 5. Onset of stroke within half a year; 6. The patients should be conscious, with stable vital signs; 7. The Patients or their legal guardians have already agreed on participating in this clinical research and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with severe vision, hearing impairment or mental disorders that would impede cognitive disorders; 2. Patients with severe unilateral spatial neglect which would impede the operating of RehaCom system; 3. Patients with dementia or obvious intellectual abdication history before stroke; 4. Associated with severe heart disease, liver, kidney failure, ancer, alimentary tract hemorrhage which could impede the cognitive evaluation and training; 5. Pregnant and lactating women; 6. Patients with cardiac pacemaker; 7. Patients participating in other clinical trials that would affect the evaluation results of this study.

Design outcomes

Primary

MeasureTime frame
Mini-Mental State Examination (MMSE);Montreal Cognitive Assessment (MoCA);

Secondary

MeasureTime frame
detection of region of interest with functional magnetic resonance;detection of brain electrical signal with ERP;Functional Independence Measure;

Countries

China

Contacts

Public ContactChenLidian

Fujian University of Traditional Chinese Medicine

cld@fjtcm.edu.cn+86 0591-22861989

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 19, 2026