Stroke
Conditions
Interventions
Circuit group (Control group):A therapist organizes 2-4 cases of hemiplegic patients with similar limb dysfunction to undergo sequence training based on the ICF concept, which is based on the ICF conc
(2) the affected upper limb / bobath grip to reach distant objects
(3) the affected upper limb / bobath grip to reach high objects
(4) the affected upper limb (sharp hand) using chopsticks to simulate eating or (non-sharp hand) using spoons to simulate eating
(5) the affected upper limb / bobath grip to simulate the use of a cup to drink
(6) the affected hand to tie a button
(7) the affected hand to turn the pages of a book
(8) both hands to put on the clothes
(9)hands wringing the towel
(10) hands tying the shoelaces. A therapist supervised the training to ensure the quality of the training. Intervention time: 30 min/session
2 sessions/day, 5 days/week, 4 weeks.
Joint Intervention Group:Virtual reality training was performed on the basis of the ICF sequence set. Virtual reality training was performed using the Easy Brain Resuscitation virtual reality device.
2 times/day, 5 days/week, total 4 weeks.
Sponsors
Sir Run Run Shaw Hospital, Zhejiang University School of Medicine
Eligibility
Sex/Gender
All
Age
40 Years to 70 Years
Inclusion criteria
Inclusion criteria: ? patients diagnosed with stroke by computed tomography or MRI imaging and confirmed that the lesion was located in the basal ganglia region; ? first onset of the disease, and the duration of the disease were between 48 hours and three months; ? age 40-70 years old; ? upper limb and finger Brunnstrom stage III and above, thus excluding patients with severe functional impairment and unable to complete the training; ? vital signs were stable and actively cooperated with the treatment; ? voluntarily enrolled in this study and signed informed consent. Vital signs were stable and actively cooperated with the treatment; ? Voluntary enrollment in this study and signing of informed consent.
Exclusion criteria
Exclusion criteria: ? Combined with other diseases remaining on the affected side of the upper limb dysfunction; ? cognitive dysfunction; ? visual and auditory dysfunction; ? unclear consciousness, can not cooperate with the treatment; ? combined with other serious diseases such as severe heart failure, malignant tumors, emphysema, etc. is not suitable for the training of the patients; ? allergic to the materials worn in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fugl-Meyer ; | — |
Secondary
| Measure | Time frame |
|---|---|
| Hong Kong version of the Functional Test for the Hemiplegic Upper Extremity,FTHUE-HK;Modified Barthel Scale;Stroke Impact Scale,SIS; | — |
Countries
China
Contacts
Public ContactYang Liu
Sir Run Run Shaw Hospital, Zhejiang University School of Medicine
Outcome results
None listed