Cerebral Infarction
Conditions
Interventions
None listed
Sponsors
Kansai Medical Univerisity
Hyogo Medical University Hospital Konan Medical Center Uonuma Kikan Hospital Hanwa Memorial Hospital Kyorin University Hospital Kitasato University Hospital Hoshigaoka Medical Center Japanese Red Cross Aichi Medical Center Nagoya Daiichi Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients with cerebral infarction who were hospitalized and prescribed rehabilitation within 7 days of onset. 2. Patients aged 65 years or older at the time of consent acquisition. 3. Patients who, after receiving a thorough explanation of the study, provided informed consent based on a full understanding and their own free will.
Exclusion criteria
Exclusion criteria: 1. Patients hospitalized for transient ischemic attack (including those who developed cerebral infarction after hospitalization for transient ischemic attack). 2. Patients hospitalized for intracerebral hemorrhage or subarachnoid hemorrhage. 3. Patients for whom end-of-life care is indicated. 4. Patients whose initial rehabilitation intervention occurred more than 8 days after admission. 5. Patients discharged within one week of admission. 6. Patients who developed cerebral infarction during hospitalization at their own or another facility. 7. Individuals who declined participation in the study. 8. Patients deemed unsuitable for inclusion by the principal investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| modified Rankin Scale at 1 year after stroke | — |
Secondary
| Measure | Time frame |
|---|---|
| Readmission within one year after onset Stroke recurrence within one year after onset Occurrence of cardiovascular events within one year after onset Patient-reported outcomes at one year after onset Incidence of falls within one year after onset Adverse events during hospitalization | — |
Countries
Japan
Contacts
Public ContactTomoyuki Ogino
Hyogo Medical University Faculty of Rehabilitation
Outcome results
None listed