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https://ir.csmu.edu.tw:8080/ir/handle/310902500/19271
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题名: | A controlled pilot trial of two commercial video games for rehabilitation of arm function after stroke |
作者: | MH, Chen LL, Huang CF, Lee CL, Hsieh YC, Lin Liu, H MI, Chen WS, Lu |
贡献者: | 中山醫學大學 |
关键词: | Commercial video game;stroke;upper extremity rehabilitation |
日期: | 2015-07 |
上传时间: | 2018-06-22T03:29:01Z (UTC)
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出版者: | Clin Rehabil |
ISSN: | 0269-2155 |
摘要: | OBJECTIVES:
To investigate the acceptability and potential efficacy of two commercial video games for improving upper extremity function after stroke in order to inform future sample size and study design.
DESIGN:
A controlled clinical trial design using sequential allocation into groups.
SETTING:
A clinical occupational therapy department.
SUBJECTS:
Twenty-four first-stroke patients.
INTERVENTIONS:
Patients were assigned to one of three groups: conventional group, Wii group, and XaviX group. In addition to regular one-hour conventional rehabilitation, each group received an additional half-hour of upper extremity exercises via conventional devices, Wii games, or XaviX games, for eight weeks.
MAIN MEASURES:
The Fugl-Meyer Assessment of motor function, Box and Block Test of Manual Dexterity, Functional Independence Measure, and upper extremity range of motion were used at baseline and postintervention. Also, a questionnaire was used to assess motivation and enjoyment.
RESULTS:
The effect size of differences in change scores between the Wii and conventional groups ranged from 0.71 (SD 0.59) to 0.28 (SD 0.58), on the Fugl-Meyer Assessment of motor function (d = 0.74) was larger than that between the XaviX and conventional groups, ranged from 0.44 (SD 0.49) to 0.28 (SD 0.58) (d = 0.30). Patient enjoyment was significantly greater in the video game groups (Wii mean 4.25, SD 0.89; XaviX mean 4.38, SD 0.52) than in the conventional group (mean 2.25, SD 0.89, F = 18.55, p < 0.001), but motivation was not significantly different across groups.
CONCLUSION:
Patients were positive to using video games in rehabilitation. A sample size of 72 patients (24 per group) would be appropriate for a full study. |
URI: | http://dx.doi.org/10.1177/0269215514554115 https://ir.csmu.edu.tw:8080/ir/handle/310902500/19271 |
關聯: | Clin Rehabil. 2015 Jul;29(7):674-82 |
显示于类别: | [職能治療學系暨碩士班] 期刊論文
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