cerebral hemorrhage Chronic, hemorrhage, brain
Conditions
Interventions
Using a tele-rehabilitation system that connect the the investigator and the subject, the subject will carry out rehabilitation via screen once a week for about an hour for six months under the guidan
tele-rehabilitation, hemorrhage, brain, application
Sponsors
Kawabori Masahito
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients who have completed the 6-month evaluation of the RAINBOW-Hx study. 2. Patients who can understand how to use the tele-rehabilitation system. 3. Patients who have received a sufficient explanation of their participation in this study and can provide written consent of their own free will after fully understanding the study. If the patient is unable to sign the document themselves, a proxy may sign it. However, written consent by a proxy will not be accepted if the patient is not fully capable of understanding or expressing their will.
Exclusion criteria
Exclusion criteria: 1. Patients who experienced a serious adverse event (SAE) in the RAINBOW-Hx study or who have continued to experience moderate or severe adverse events since the RAINBOW-Hx study, and who are judged by the principal investigator to be at high risk for safety. 2. Patients who are otherwise judged by the principal investigator or co-investigators to be inappropriate as subjects.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety of rehabilitation using a tele-rehabilitation system up to 6 months after the start of the program | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate the feasibility of rehabilitation using the tele-rehabilitation system Evaluate the change from the baseline of the RAINBOW-Hx study for the efficacy endpoints Evaluate the change from the baseline of this study for the efficacy endpoints | — |
Contacts
Public ContactArisa Miura
Hokkaido University Hospital
Outcome results
None listed