Cerrada Christian J, Weinberg Janice, Sherman Karen J, Saper Robert B
Department of Family Medicine, Boston University School of Medicine and Boston Medical Center, 1 Boston Medical Center Place, Dowling 5 South, Boston, MA 02118, USA.
BMC Res Notes. 2014 Apr 9;7:227. doi: 10.1186/1756-0500-7-227.
Little is known about the reliability of different methods of survey administration in low back pain trials. This analysis was designed to determine the reliability of responses to self-administered paper surveys compared to computer assisted telephone interviews (CATI) for the primary outcomes of pain intensity and back-related function, and secondary outcomes of patient satisfaction, SF-36, and global improvement among participants enrolled in a study of yoga for chronic low back pain.
Pain intensity, back-related function, and both physical and mental health components of the SF-36 showed excellent reliability at all three time points; ICC scores ranged from 0.82 to 0.98. Pain medication use showed good reliability; kappa statistics ranged from 0.68 to 0.78. Patient satisfaction had moderate to excellent reliability; ICC scores ranged from 0.40 to 0.86. Global improvement showed poor reliability at 6 weeks (ICC = 0.24) and 12 weeks (ICC = 0.10).
CATI shows excellent reliability for primary outcomes and at least some secondary outcomes when compared to self-administered paper surveys in a low back pain yoga trial. Having two reliable options for data collection may be helpful to increase response rates for core outcomes in back pain trials.
ClinicalTrials.gov: NCT01761617. Date of trial registration: December 4, 2012.
在腰痛试验中,对于不同调查管理方法的可靠性了解甚少。本分析旨在确定在一项针对慢性腰痛的瑜伽研究中,与计算机辅助电话访谈(CATI)相比,自我填写纸质调查问卷对于疼痛强度和背部相关功能等主要结局,以及患者满意度、SF-36和整体改善情况等次要结局的回答可靠性。
在所有三个时间点,疼痛强度、背部相关功能以及SF-36的生理和心理健康分量表均显示出极佳的可靠性;组内相关系数(ICC)得分在0.82至0.98之间。止痛药物使用情况显示出良好的可靠性;kappa统计量在0.68至0.78之间。患者满意度具有中等至极佳的可靠性;ICC得分在0.40至0.86之间。整体改善情况在6周(ICC = 0.24)和12周(ICC = 0.10)时显示出较差的可靠性。
在腰痛瑜伽试验中,与自我填写纸质调查问卷相比,CATI对于主要结局以及至少部分次要结局显示出极佳的可靠性。拥有两种可靠的数据收集方式可能有助于提高腰痛试验中核心结局的应答率。
ClinicalTrials.gov:NCT01761617。试验注册日期:2012年12月4日。