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Comparative Effectiveness of Chuna Manipulative Therapy for Non-Acute Lower Back Pain: A Multi-Center Pragmatic Randomized Controlled Trial

机译:Chuna手法治疗非急性下腰痛的比较效果:多中心实用随机对照试验

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摘要

Current evidence on the effectiveness and safety of Chuna manipulative therapy (CMT) for managing non-acute lower back pain (LBP) is insufficient. We investigated the comparative effectiveness and safety of CMT, a Korean style of manipulation, plus usual care (UC) compared to UC alone for non-acute LBP. We conducted a parallel, two-armed, multi-centered, assessor blinded, pragmatic, randomized controlled trial at four major Korean medical hospitals. Overall, 194 patients were randomly allocated to either CMT plus UC ( = 97) or UC alone ( = 97), for six weeks of treatment and six months follow-up. The primary outcome was measured using the numerical rating scale (NRS) of LBP intensity at 7 weeks. Secondary outcomes included NRS of leg pain, Oswestry Disability Index (ODI) for functional disability, patient global impression of change (PGIC) scale, and safety. A total of 194 patients were included in the intention-to-treat analysis, and 174 patients provided complete data for the primary outcome. At 7 weeks, clinically significant differences between groups were observed in the NRS of LBP (CMT + UC: −3.02 ± 1.72, UC: −1.36 ± 1.75, < 0.001), ODI scores (CMT + UC: −5.65 ± 4.29, UC: −3.72 ± 4.63, = 0.003), NRS of leg pain (CMT + UC: −2.00 ± 2.33, UC: −0.44 ± 1.86, < 0.0001), and PGIC (CMT + UC: −0.28 ± 0.85, UC: 0.01 ± 0.66, = 0.0119). Mild to moderate safety concerns were reported in 21 subjects. CMT plus UC showed higher effectiveness compared to UC alone in patients with non-acute LBP in reducing LBP and leg pain and in improving function with good safety results using a powered sample size and including mid-term follow-up.
机译:有关Chuna手法治疗非急性下背痛(LBP)的有效性和安全性的现有证据不足。我们调查了非急性LBP与单独使用UC相比,CMT,韩国操作方式以及常规护理(UC)的相对有效性和安全性。我们在韩国的四家主要医院进行了平行,两臂,多中心,评估者盲目,务实,随机对照试验。总体而言,有194名患者被随机分配接受CMT加UC(= 97)或仅接受UC(= 97)治疗,疗程为6周,为期6个月。使用7周时LBP强度的数字量表(NRS)测量主要结局。次要结果包括腿痛的NRS,功能障碍的Oswestry残疾指数(ODI),患者对变化的整体印象(PGIC)量表和安全性。意向治疗分析共纳入194例患者,其中174例患者提供了主要结果的完整数据。在第7周时,各组之间在LBP的NRS(CMT + UC:−3.02±1.72,UC:−1.36±1.75,<0.001),ODI评分(CMT + UC:−5.65±4.29,UC)之间观察到临床上的显着差异:-3.72±4.63,= 0.003),腿痛的NRS(CMT + UC:-2.00±2.33,UC:-0.44±1.86,<0.0001),以及PGIC(CMT + UC:-0.28±0.85,UC:0.01 ±0.66,= 0.0119)。据报道有21位受试者有轻度至中度的安全隐患。与非急性LBP患者相比,CMT加UC在单独使用非常规LBP的患者(包括中期随访)减轻LBP和腿痛以及改善功能方面具有更高的有效性,并具有良好的安全性。

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