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Evaluation research of rehabilitation outcome of traditional Chinese medicine on stroke

Evaluation research of rehabilitation outcome of traditional Chinese medicine on stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034293
Enrollment
Unknown
Registered
2020-07-01
Start date
2020-07-16
Completion date
Unknown
Last updated
2020-07-06

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

Conditions

Stroke

Interventions

case series:Nil

Sponsors

The Affiliated People's Hospital of Fujian University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who meet the diagnostic criteria of stroke and are confirmed by CT or MRI; 2. Inpatients; 18 years old 24 in middle school and above, MMSE > 20 in primary school, MMSE > 17 in illiterate; 4. Patients with different degrees of limb motor dysfunction caused by stroke; 5. Patients with stable condition and conscious consciousness; 6. Patients without obvious communication barriers; 7. For patients who voluntarily sign the informed consent form, if the subjects are unable to sign, their immediate relatives or guardians will sign the informed consent on behalf of them.

Exclusion criteria

Exclusion criteria: 1. Patients with other brain diseases, such as inflammation, infection, tumor and other brain damage sequelae; 2. Stroke patients without neurological deficit sequelae, such as transient ischemic attack (TIA), lacunar infarction, etc; 3. Patients with severe visual or hearing impairment, mental disorder and other factors that affect normal answering; 4. Patients with obvious mental retardation and dementia before onset; 5. Patients with severe heart, liver, kidney, endocrine and hematopoietic diseases; 6. Pregnant and lactating women; 7. Patients who are unwilling to cooperate or cannot tolerate the test; 8. Patients who are participating in other clinical trials affecting the evaluation of the results of this study.

Design outcomes

Primary

MeasureTime frame
Mini-Mental State Examination, MMSE;Fugl-Meyer, FMA;Modified Barthel Index, MBI;Montreal Cognitive Assessment, MoCA;

Secondary

MeasureTime frame
Oxford Cognitive Screen - Putonghua;SS-QOL;

Countries

China

Contacts

Public ContactBin Chen

The Affiliated People's Hospital of Fujian University of Traditional Chinese Medicine

chenbin327425224@163.com+86 15980273832

Outcome results

None listed

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