upper limb motor dysfunction of stroke patient
Conditions
Interventions
Study Four-Control Group:task-oriented training was performed for the patients' upper limb motor dysfunction
Study Four-VR Intervention group:Based on the patients performance in the 19 items covering four aspects (grasping, gripping, pinching, and gross motor skills) in the ARAT assessment, as well as the s
Study Two-experimental group:Receive VR-ARAT and ARAT scale assessments. On Day 1 (baseline assessment), in a random order, first conduct the traditional ARAT assessment, that is, complete 19 tasks in
Study Two-Control Group 1: On Day 1 (baseline assessment), conduct the traditional ARAT assessment and ARAT-VR assessment in a random order, following a process similar to that of the experimental gro
Study Two-Control Group 2:Complete the traditional ARAT and ARAT-VR assessments respectively. Use a Likert scale (-2 to +2) to evaluate the consistency of difficulty between VR tasks and real tas
Sponsors
Jiangsu Medical College
Eligibility
Sex/Gender
All
Age
35 Years to 70 Years
Inclusion criteria
Inclusion criteria: The inclusion criteria are the same across all studies.1. Meet the diagnostic criteria of stroke, and have cerebral hemorrhage or cerebral infarction confirmed by computed tomography (CT) or magnetic resonance imaging (MRI) 2: 3. Age 35-70 years old 3: 4.ARAT > 15 points, and can actively and independently complete the task of grasping and placing a 5cm wooden block 4: 5. Stable condition without severe cognitive impairment (MoCA>=26), able to cooperate with therapists to complete the trial 5: 6. Visual field is intact or normal after correction 6: 7. No obvious VR motion sickness, can tolerate the test 7: 8. Voluntarily participate in this experiment and agree to sign an informed consent form.
Exclusion criteria
Exclusion criteria: The exclusion criteria are the same across all studies.1. History of traumatic brain injury, Parkinson's disease, mental illness, or drug or alcohol abuse 2. Severe comprehensive aphasia and difficulty in following therapist's instructions 3. Severe hearing loss 4. Unilateral neglect and visual impairment 5. Severe sensory dysfunction of the hemiplegic upper limb (SWMT of the hemiplegic thumb monofilament tactile test between grades 1 and 3) 6. Significant upper limb pain (VAS>4) 7. Obvious VR motion sickness, unable to tolerate the test 8. Important organ failure or other critical diseases 9. No informed consent was obtained.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Action Research Arm Test (Study Two/Four); | — |
Secondary
| Measure | Time frame |
|---|---|
| Electroencephalography data(Study Four);Surface Electromyography (Study Four);Functional Near-Infrared Spectroscopy (Study Three/Four);Nine-Hole Peg Test (Study Four);Modified Barthel Index (Study Four);Kinematic Parameter (Study Two/Four);Purdue Pegboard Test (Study Four);Montreal Cognitive Assessment (Study Four); | — |
Countries
China
Contacts
Public ContactSu Bin
Jiangsu Medical College
Outcome results
None listed