评估瑞典版国际瀑布功效量表(FES-I)

E. Nordell, M. Andreasson, Karin Gall, K. Thorngren
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引用次数: 68

摘要

有许多测量跌倒心理结果的工具,例如跌倒效能量表(FES)。FES的扩展版本,即国际瀑布功效量表(FES- i),已被开发并翻译成几种欧洲语言。本研究的目的是评估内部信度,检查FES-I(S)(瑞典版FES-I)的内部结构,并检查跌倒恐惧与用短表格12 (SF-12)测量的健康相关生活质量之间的相关性。86名参与者,年龄50-85岁(88%为女性),从隆德大学医院骨科招募,并接受跌倒相关骨折治疗,回答了FES-I(S), SF-12和背景因素问卷。FES-I(S)具有较高的内部信度(Cronbach’S α=0.95)和平均0.55的项目间相关。因子分析分别区分了体力活动要求较低项目和体力活动要求较高项目占主导的两个因子。FES-I(S)和SF-12生理成分得分与FES-I(S)和SF-12心理成分得分之间的Spearman等级相关系数分别为- 0.591和- 0.402,显著相关(p=0.01)。FES-I(S)将在瑞典的康复研究和临床试验中用于评估对跌倒的恐惧。建议进一步的研究来验证FES-I(S)的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating the Swedish version of the Falls Efficacy Scale-International (FES-I)
A number of instruments measuring psychological outcomes of falling exist, e.g. the Falls Efficacy Scale (FES). An extended version of the FES, the Falls Efficacy Scale-International (FES-I), has been developed and translated into several European languages. The aims of this study were to evaluate internal reliability, examine the internal structure of the FES-I(S) (the Swedish version of the FES-I), and to examine the correlation between fear of falling and health-related quality of life measured with Short Form 12 (SF-12). Eighty-six participants, aged 50–85 years (88% women), recruited from the Orthopaedic Department, Lund University Hospital, and treated for a fall-related fracture, answered the FES-I(S), SF-12 and a questionnaire of background factors. The FES-I(S) showed a high internal reliability (Cronbach's α=0.95) and an inter-item correlation averaging 0.55. Factor analyses discriminated two factors dominated by items of less and more demanding physical activities, respectively. All items loaded strongly on a unitary underlying dimension There were significant correlations (p=0.01) between the FES-I(S) and SF-12 physical component score and the FES-I(S) and SF-12 mental component score with Spearman's rank correlation coefficient of −0.591 and −0.402, respectively. The FES-I(S) will be useful to assess fear of falling in Sweden in rehabilitation research and in clinical trials. Further studies are suggested to verify FES-I(S) validity.
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