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A randomized controlled trial on the efficacy of intermittent cervical traction for patients with chronic neck pain.

机译:间歇性颈椎牵引治疗慢性颈痛的疗效的随机对照试验。

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OBJECTIVE: To investigate the efficacy of intermittent cervical traction in the treatment of chronic neck pain over a 12-week follow-up. DESIGN: A randomized controlled trial. SETTING: Hospital-based outpatient practice. SUBJECTS: Seventy-nine patients with chronic neck pain. INTERVENTIONS: Subjects were randomly assigned to either experimental group (n = 39, mean age = 50.5 +/- 9.8) or control group (n = 40, mean age = 48.8 +/- 9.1). Experimental group received intermittent cervical traction and control group received infrared irradiation alone; twice a week over a period of six weeks. OUTCOME MEASUREMENTS: The values of Chinese version of the Northwick Park Neck Pain Questionnaire (NPQ), verbal numerical pain scale (VNPS), and cervical active range of motion (AROM) were measured at baseline, six-week and 12-week follow-up. RESULTS: No significant differences were found between the two groups in the NPQ (P > 0.05), VNPS (P > 0.05) and AROM (P > 0.05).
机译:目的:探讨间歇性颈椎牵引治疗慢性颈痛的疗效,历时12周。设计:一项随机对照试验。地点:基于医院的门诊实践。受试者:79例慢性颈部疼痛患者。干预措施:将受试者随机分为实验组(n = 39,平均年龄= 50.5 +/- 9.8)或对照组(n = 40,平均年龄= 48.8 +/- 9.1)。实验组采用间歇性颈椎牵引,对照组仅采用红外辐射。在六个星期的时间内每周两次。结果测量:在基线,六周和十二周随访时,测量中文版《诺斯威克公园颈部疼痛问卷》(NPQ),口头数字疼痛量表(VNPS)和宫颈活动范围(AROM)的值。向上。结果:两组在NPQ(P> 0.05),VNPS(P> 0.05)和AROM(P> 0.05)之间均无显着差异。

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