首页> 外文期刊>Pain. >The effect of 300 mW, 830 nm laser on chronic neck pain: a double-blind, randomized, placebo-controlled study.
【24h】

The effect of 300 mW, 830 nm laser on chronic neck pain: a double-blind, randomized, placebo-controlled study.

机译:300 mW,830 nm激光对慢性颈部疼痛的影响:一项双盲,随机,安慰剂对照研究。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

A randomized, double-blind, placebo-controlled study of low-level laser therapy (LLLT) in 90 subjects with chronic neck pain was conducted with the aim of determining the efficacy of 300 mW, 830 nm laser in the management of chronic neck pain. Subjects were randomized to receive a course of 14 treatments over 7 weeks with either active or sham laser to tender areas in the neck. The primary outcome measure was change in a 10 cm Visual Analogue Scale (VAS) for pain. Secondary outcome measures included Short-Form 36 Quality-of-Life questionnaire (SF-36), Northwick Park Neck Pain Questionnaire (NPNQ), Neck Pain and Disability Scale (NPAD), the McGill Pain Questionnaire (MPQ) and Self-Assessed Improvement (SAI) in pain measured by VAS. Measurements were taken at baseline, at the end of 7 weeks' treatment and 12 weeks from baseline. The mean VAS pain scores improved by 2.7 in the treated group and worsened by 0.3 in the control group (difference 3.0, 95% CI 3.8-2.1). Significant improvements were seen in theactive group compared to placebo for SF-36-Physical Score (SF36 PCS), NPNQ, NPAD, MPQVAS and SAI. The results of the SF-36 - Mental Score (SF36 MCS) and other MPQ component scores (afferent and sensory) did not differ significantly between the two groups. Low-level laser therapy (LLLT), at the parameters used in this study, was efficacious in providing pain relief for patients with chronic neck pain over a period of 3 months.
机译:进行了一项随机,双盲,安慰剂对照研究,对90例慢性颈痛患者进行了低水平激光治疗(LLLT),旨在确定300 mW,830 nm激光对慢性颈痛的治疗效果。受试者被随机接受主动或假激光在7周内接受14疗程的治疗,以治疗颈部的压痛部位。主要的预后指标是疼痛的10厘米视觉模拟量表(VAS)的变化。次要结果指标包括简短的36型生活质量问卷(SF-36),诺斯威克公园颈部疼痛问卷(NPNQ),颈部疼痛和残疾量表(NPAD),麦吉尔疼痛问卷(MPQ)和自我评估的改善(SAI)通过VAS测量疼痛。在基线,治疗7周结束时和距基线12周时进行测量。在治疗组中,VAS平均疼痛评分提高了2.7,而在对照组中则降低了0.3(差异3.0,95%CI 3.8-2.1)。与安慰剂相比,活动组的SF-36生理评分(SF36 PCS),NPNQ,NPAD,MPQVAS和SAI有显着改善。两组的SF-36-心理得分(SF36 MCS)和其他MPQ组分得分(生气和感官)的结果无显着差异。在此研究中使用的参数下,低水平激光疗法(LLLT)可有效缓解3个月内慢性颈部疼痛的患者的疼痛。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号