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首页> 外文期刊>Physiotherapy >Dose-response effects of medical exercise therapy in patients with patellofemoral pain syndrome: A randomised controlled clinical trial
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Dose-response effects of medical exercise therapy in patients with patellofemoral pain syndrome: A randomised controlled clinical trial

机译:exercise股痛综合征患者药物治疗的剂量反应:一项随机对照临床试验

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摘要

Objectives: To evaluate two different therapeutic exercise regimens in patients with patellofemoral pain syndrome (PFPS). Design: Multicentre, randomised controlled clinical trial. Setting: Three primary healthcare physiotherapy clinics. Participants: Forty-two patients with PFPS were assigned at random to an experimental group or a control group. Forty participants completed the study. Interventions: Both groups received three treatments per week for 12 weeks. The experimental group received high-dose, high-repetition medical exercise therapy, and the control group received low-dose, low-repetition exercise therapy. The groups differed in terms of number of exercises, number of repetitions and sets, and time spent performing aerobic/global exercises. Main outcome measures: Outcome parameters were pain (measured using a visual analogue scale) and function [measured using the step-down test and the modified Functional Index Questionnaire (FIQ)]. Results: At baseline, there were no differences between the groups. After the interventions, there were statistically significant (. P<. 0.05) and clinically important differences between the groups for all outcome parameters, all in favour of the experimental group: -1.6 for mean pain [95% confidence interval (CI) -2.4 to -0.8], 6.5 for step-down test (95% CI 3.8 to 9.2) and 3.1 for FIQ (95% CI 1.2 to 5.0). Conclusion: The results indicate that exercise therapy has a dose-response effect on pain and functional outcomes in patients with PFPS. This indicates that high-dose, high-repetition medical exercise therapy is more efficacious than low-dose, low-repetition exercise therapy for this patient group.Registered on http://www.clinicaltrials.gov (identifier: NCT01290705).
机译:目的:评估pa股股骨疼痛综合征(PFPS)患者的两种不同的治疗运动方案。设计:多中心,随机对照临床试验。地点:三家初级保健理疗诊所。参与者:将42例PFPS患者随机分为实验组或对照组。四十名参与者完成了研究。干预措施:两组均每周接受三种治疗,共12周。实验组接受大剂量,高重复性的医学运动疗法,对照组接受小剂量,低重复性的运动疗法。各组的锻炼次数,重复次数和套数以及进行有氧/整体锻炼所花费的时间有所不同。主要结局指标:结果参数为疼痛(使用视觉模拟量表测量)和功能(使用降压测试和改良的功能指数问卷(FIQ)测量)。结果:基线时,两组之间没有差异。干预后,两组之间所有结局参数的统计学差异(。P <。0.05)和临床上重要的差异,均支持实验组:平均疼痛为-1.6 [95%置信区间(CI)-2.4至-0.8],降压测试为6.5(95%CI为3.8至9.2)和FIQ为3.1(95%CI为1.2至5.0)。结论:结果表明,运动疗法对PFPS患者的疼痛和功能结局具有剂量反应作用。这表明对于该患者组而言,高剂量,高重复性的医学运动疗法比低剂量,低重复性的运动疗法更有效。在http://www.clinicaltrials.gov上注册(标识:NCT01290705)。

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