1 Department of Health Sciences, Faculty of Health Sciences, University of Jaén, Jaén, Spain.
2 Unit of Pharmacology, Department of Basic Medical Sciences, Faculty of Medicine and Health Sciences, NFOC Group, Universitat Rovira i Virgili, Reus, Spain.
Clin Rehabil. 2018 Sep;32(9):1249-1257. doi: 10.1177/0269215518768393. Epub 2018 Apr 13.
To assess the effectiveness of 12 weeks of Pilates practice on disability, pain and kinesiophobia in patients with chronic non-specific low back pain.
This is a randomized controlled trial.
This study was conducted in the university laboratory.
A total of 64 participants with chronic non-specific low back pain were included.
Participants were randomly allocated to intervention group consisted in Pilates intervention during 12 weeks ( n = 32) or control group who received no treatment ( n = 32).
Disability, pain and kinesiophobia were assessed by Roland Morris Disability Questionnaire, visual analogue scale and Tampa Scale of Kinesiophobia, respectively. Measurements were performed at baseline, at 6 and 12 weeks after study completion.
There were significant differences between groups with observed improvement in Pilates intervention group in all variables after treatment ( P < 0.001). Major changes on disability and kinesiophobia were observed at six weeks of intervention with no significant difference after 12 weeks ( P < 0.001). Mean changes of the intervention group compared with the control group were 4.00 (0.45) on the Roland Morris Disability Questionnaire and 5.50 (0.67) in the Tampa Scale of Kinesiophobia. Pain showed better results at six weeks with a slightly but statistically significant improvement at 12 weeks with Visual Analogue Scale scores of 2.40 (0.26) ( P < 0.001).
Pilates intervention in patients with chronic non-specific low back pain is effective in the management of disability, pain and kinesiophobia.
评估 12 周普拉提练习对慢性非特异性下腰痛患者残疾、疼痛和运动恐惧的疗效。
这是一项随机对照试验。
本研究在大学实验室进行。
共纳入 64 例慢性非特异性下腰痛患者。
参与者被随机分配到干预组( n =32),接受 12 周的普拉提干预,或对照组( n =32),不接受任何治疗。
使用罗尔登莫里斯残疾问卷、视觉模拟评分和坦帕运动恐惧量表分别评估残疾、疼痛和运动恐惧。在基线、研究完成后 6 周和 12 周进行测量。
在治疗后,普拉提干预组在所有变量上均有显著差异( P < 0.001)。在干预 6 周后,运动恐惧和残疾方面有显著改善,12 周后无显著差异( P < 0.001)。与对照组相比,干预组的平均变化在罗尔登莫里斯残疾问卷上为 4.00(0.45),在坦帕运动恐惧量表上为 5.50(0.67)。疼痛在 6 周时有更好的结果,12 周时有轻微但统计学上显著的改善,视觉模拟评分 2.40(0.26)( P < 0.001)。
普拉提干预慢性非特异性下腰痛患者在管理残疾、疼痛和运动恐惧方面是有效的。