| Literature DB >> 23035951 |
Youn Joo Kang1, Hae Kyung Park, Hyun Jung Kim, Taeo Lim, Jeonghun Ku, Sangwoo Cho, Sun I Kim, Eun Sook Park.
Abstract
BACKGROUND: Several experimental studies in stroke patients suggest that mirror therapy and various virtual reality programs facilitate motor rehabilitation. However, the underlying mechanisms for these therapeutic effects have not been previously described.Entities:
Mesh:
Year: 2012 PMID: 23035951 PMCID: PMC3543207 DOI: 10.1186/1743-0003-9-71
Source DB: PubMed Journal: J Neuroeng Rehabil ISSN: 1743-0003 Impact factor: 4.262
Demographic and clinical characteristics of stroke patients
| 1 | M | 64 | 5 | Infarction | Rt. Th (subcortical) | 96 |
| 2 | F | 45 | 12 | Infarction | Rt. BG (subcortical) | 116 |
| 3 | F | 50 | 9 | Hemorrhage | Rt. BG (subcortical) | 112 |
| 4 | F | 77 | 20 | Infarction | Rt. pontine | 87 |
| 5 | M | 67 | 6 | Infarction | Lt. Th (subcortical) | 98 |
| 6 | M | 50 | 47 | Infarction | Lt. Th (subcortical) | 120 |
| 7 | F | 54 | 96 | Infarction | Rt. BG (subcortical) | 126 |
| 8 | M | 63 | 20 | Hemorrhage | Rt. Th (subcortical) | 114 |
| 9 | M | 61 | 5 | Infarction | Rt. BG (subcortical) | 90 |
| 10 | M | 69 | 7 | Hemorrhage | Lt. P,O (cortical and subcortical) | 100 |
| 11 | M | 72 | 6 | Infarction | Lt. BG, Th (subcortical) | 92 |
| 12 | M | 72 | 16 | Infarction | Lt. CR (cortical and subcortical) | 76 |
| 13 | M | 50 | 40 | Hemorrhage | Rt. F, P (subcortical) | 91 |
| 14 | M | 71 | 5 | Infarction | Rt. BG, Th (subcortical) | 86 |
| 15 | F | 65 | 8 | Infarction | Rt. BG (subcortical) | 100 |
| 16 | M | 70 | 6 | Infarction | Rt. F,O (cortical and subcortical) | 92 |
| 17 | M | 34 | 24 | Hemorrhage | Rt. cerebellum | 112 |
| 18 | F | 70 | 22 | Infarction | Lt. CR (cortical and subcortical) | 91 |
Rt., right; Lt., left; BG, basal ganglia; Th, thalamus; F, frontal lobe; P, parietal lobe; O, occipital lobe; MCA, middle cerebral artery; CR, corona radiata.
Figure 1Setup of the real mirror (A) and virtual mirror (B) experiments. In the virtual mirror task, the subjects wore a head-mounted display while sitting in front of a table. The left upper extremity of healthy subjects, or the unaffected upper extremity of stroke patients, was placed on the experimental device, which records the angle of the wrist movements. Subjects could see a virtual cup on a virtual table and a virtual upper extremity contralateral to the moving upper extremity through the head-mounted display. The movements of the virtual upper extremity were controlled by the movements of the real moving upper extremity.
Figure 2Setup of the continuous visual feedback (A) and intermittent visual feedback (B) experiments. During the task (A), participants could see a virtual left upper extremity (affected arm in the stroke group) continuously during exercise. However, during task (B), the virtual upper extremity and cup became invisible, so that participants had to find the exact position of the virtual cup in the virtual environment using his or her own cognitive domain.
Figure 3Facilitation of MEPs during the virtual mirror program in healthy subjects and stroke patients. The amplitude increment and latency decrement of MEPs in healthy subjects and stroke patients were significantly greater in the virtual mirror paradigm than in the real mirror exercise (repeated measures ANOVA; ***P <0.001).
Figure 4Facilitation of MEPs during visual-feedback-controlled virtual mirror exercise in healthy subjects and stroke patients. The amplitude increment and latency decrement of MEPs in healthy subjects and stroke patients were significantly greater for the intermittent visual feedback program (mode 2) than for the continuous visual feedback program(mode 1) (independent two sample t-test; **P <0.01).