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两种评估健康年轻成年人压力疼痛阈值方案的可靠性

Reliability of 2 protocols for assessing pressure pain threshold in healthy young adults.

作者信息

Bisset Leanne M, Evans Kerrie, Tuttle Neil

机构信息

Senior Lecturer, Griffith Health Institute, Griffith University, Gold Coast, Queensland, Australia.

Senior Lecturer, Griffith Health Institute, Griffith University, Gold Coast, Queensland, Australia.

出版信息

J Manipulative Physiol Ther. 2015 May;38(4):282-7. doi: 10.1016/j.jmpt.2015.03.001. Epub 2015 Apr 27.

DOI:10.1016/j.jmpt.2015.03.001
PMID:25925018
Abstract

OBJECTIVE

The purposes of this study were to determine whether there were differences in mean values or reliability for 2 frequently used protocols for pressure pain threshold (PPT) and to calculate how large a difference in PPT is necessary to be 95% confident that a real change has occurred.

METHODS

Thirteen participants (8 females) aged 22.3 (±2.3) years from a university community were included. Two testers evaluated participants using 2 protocols, in which PPT was measured 3 times at 8 different body locations. The "cluster protocol" consisted of 3 successive measurements at each location with a 30-second rest between each measurement. The "circuit protocol" consisted of 1 measurement taken at each anatomical location until "the circuit" was complete and then repeated a total of 3 times.

RESULTS

A 2-way analysis of variance did not reveal significant differences between protocols at any body location (P = .46-.98). Intertester reliability was good to excellent for all locations (intraclass correlation coefficient, 0.84-0.96), and limits of agreement ranged from 108 to 223 kPa.

CONCLUSIONS

Either the cluster or circuit protocol can be used to measure PPT in clinical or research setting. A difference of 160 kPa is considered sufficient to indicate a real difference between repeated measures of PPT regardless of protocol used for testing.

摘要

目的

本研究旨在确定两种常用的压力痛阈(PPT)测量方案在平均值或可靠性方面是否存在差异,并计算出PPT需要有多大差异才能有95%的把握确定发生了真实变化。

方法

纳入了来自大学社区的13名参与者(8名女性),年龄为22.3(±2.3)岁。两名测试者使用两种方案对参与者进行评估,在8个不同身体部位测量PPT 3次。“聚类方案”包括在每个部位连续进行3次测量,每次测量之间休息30秒。“循环方案”包括在每个解剖部位进行1次测量,直到“循环”完成,然后总共重复3次。

结果

双向方差分析未显示在任何身体部位两种方案之间存在显著差异(P = 0.46 - 0.98)。所有部位的测试者间可靠性良好至优秀(组内相关系数,0.84 - 0.96),一致性界限范围为108至223 kPa。

结论

聚类方案或循环方案均可用于临床或研究环境中测量PPT。无论使用何种测试方案,PPT重复测量之间相差160 kPa被认为足以表明存在真实差异。

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