Bronfort Gert, Evans Roni L, Maiers Michele, Anderson Alfred V
Wolfe-Harris Center for Clinical Studies, Northwestern Health Sciences University, Bloomington, MN 55431, USA.
J Manipulative Physiol Ther. 2004 Oct;27(8):503-8. doi: 10.1016/j.jmpt.2004.08.002.
To assess the feasibility of recruiting sciatica patients and to evaluate their compliance in preparation for a full-scale randomized clinical trial. We also aimed to determine the responsiveness of key outcome measures.
Thirty-two subjects were randomly assigned to spinal manipulation (n=11), epidural steroid injections (n=11), or self-care education (n=10). No between-group comparisons were planned because of the small sample size.
At week 12 (the end of the treatment phase), the outcome measures indicating the most improvement/change were the Oswestry disability score (mean, 22.9; SD, 19.9; effect size [ES], 1.8), leg pain severity (mean, 2.9; SD, 1.7; ES, 1.7), and if the symptoms were bothersome (mean, 25.2; SD, 16.0; ES, 1.6). Twenty-four patients were either "very satisfied" or "completely satisfied," and 22 of 32 patients reported 75% or 100% improvement. After 52 weeks, the outcome measure showing the most improvement/change was leg pain severity (mean, 2.3; SD, 2.6; ES, 1.35), followed by the Oswestry disability score (mean, 15.6; SD, 20; ES, 1.2) and if symptoms were bothersome (mean, 18.1; SD, 22.6; ES, 1.1). Eighteen patients were either "very satisfied" or "completely satisfied," and 15 of 32 patients reported 75% or 100% improvement.
The results of this pilot study suggest that it is feasible to recruit subacute and chronic sciatica patients and to obtain their compliance for a full-scale randomized clinical.
评估招募坐骨神经痛患者的可行性,并评估他们为全面随机临床试验做准备时的依从性。我们还旨在确定关键结局指标的反应性。
32名受试者被随机分配至脊柱推拿组(n = 11)、硬膜外类固醇注射组(n = 11)或自我护理教育组(n = 10)。由于样本量小,未计划进行组间比较。
在第12周(治疗阶段结束时),显示改善/变化最大的结局指标是Oswestry功能障碍评分(均值为22.9;标准差为19.9;效应量[ES]为1.8)、腿痛严重程度(均值为2.9;标准差为1.7;ES为1.7)以及症状是否困扰(均值为25.2;标准差为16.0;ES为1.6)。24名患者“非常满意”或“完全满意”,32名患者中有22名报告改善了75%或100%。52周后,显示改善/变化最大的结局指标是腿痛严重程度(均值为2.3;标准差为2.6;ES为1.35),其次是Oswestry功能障碍评分(均值为15.6;标准差为20;ES为1.2)以及症状是否困扰(均值为18.1;标准差为22.6;ES为1.1)。18名患者“非常满意”或“完全满意”,32名患者中有15名报告改善了75%或100%。
这项初步研究的结果表明,招募亚急性和慢性坐骨神经痛患者并使其依从全面随机临床试验是可行的。