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靶向运动对前交叉韧带重建术后股后肌群持续缺损患者膝关节肌肉功能的影响——一项随机对照试验的研究方案

The effect of targeted exercise on knee-muscle function in patients with persistent hamstring deficiency following ACL reconstruction - study protocol for a randomized controlled trial.

作者信息

Bregenhof Bo, Jørgensen Uffe, Aagaard Per, Nissen Nis, Creaby Mark W, Thorlund Jonas Bloch, Jensen Carsten, Torfing Trine, Holsgaard-Larsen Anders

机构信息

Orthopaedic Research Unit, Department of Orthopaedics and Traumatology, Odense University Hospital, Institute of Clinical Research, University of Southern Denmark, Sdr. Boulevard 29, 5000, Odense C, Denmark.

Department of Orthopaedics, Lillebaelt Hospital, Kolding, Skovvangen 2-8, 6000, Kolding, Denmark.

出版信息

Trials. 2018 Jan 26;19(1):75. doi: 10.1186/s13063-018-2448-3.

Abstract

BACKGROUND

Anterior cruciate ligament (ACL) reconstruction, using hamstring auto-graft is a common surgical procedure, which often leads to persistent hamstring muscle-strength deficiency and reduced function. The purpose of this randomized controlled trial (RCT) is to investigate the effect of a combined, progressive, strength and neuromuscular exercise intervention on knee muscle strength, functional capacity and hamstring muscle-tendon morphology in ACL-reconstructed patients with persistent hamstring muscle-strength deficiency compared with controls.

METHODS/DESIGN: The study is designed as a multicenter, parallel-group RCT with balanced randomization (1:1) and blinded outcome assessments (level of evidence: II) and will be reported in accordance with the CONSORT Statement. Fifty ACL-reconstructed patients (hamstring auto-graft) with persistent limb-to-limb knee-flexor muscle-strength asymmetry at 12-24 months' post surgery, will be recruited through outpatient clinics and advertisements. Patients will be randomized to a 12-week progressive, strength and neuromuscular exercise group (SNG) with supervised training twice weekly or a control intervention (CON) consisting of a home-based, low-intensity exercise program. Outcome measures include between-group change in maximal isometric knee-flexor strength (primary outcome) and knee-extensor muscle strength, hamstring-to-quadriceps strength ratios of the leg that has been operated on and Knee injury and Osteoarthritis Outcome Score (KOOS) (secondary outcomes). In addition, several explorative outcomes will be investigated: The International Knee Documentation Committee Subjective Knee Form (IKDC), the Tegner Activity Score, rate of force development (RFD) for the knee flexors and extensors, tendon regeneration and potential muscle hypertrophy at graft harvest site evaluated by magnetic resonance imaging (MRI), postural control, kinetic/kinematic gait characteristics and knee-related functional capacity.

DISCUSSION

This RCT is designed to investigate the effect of combined, progressive-resistance and neuromuscular exercises on knee-flexor/extensor strength, in the late rehabilitation phase following ACL reconstruction. Reduced hamstring strength represents a potential risk factor for secondary ACL rupture and accelerated progression of osteoarthritis. If deemed effective, the intervention paradigm introduced in this study may help to improve current treatment strategies in ACL-reconstructed patients.

TRIAL REGISTRATION

ClinicalTrials.gov, ID: NCT02939677 (recruiting). Registered on 20 October 2016.

摘要

背景

使用腘绳肌自体移植物进行前交叉韧带(ACL)重建是一种常见的外科手术,该手术常导致腘绳肌力量持续不足和功能下降。本随机对照试验(RCT)的目的是研究与对照组相比,联合、渐进性、力量和神经肌肉锻炼干预对ACL重建术后腘绳肌力量持续不足患者的膝关节肌肉力量、功能能力和腘绳肌肌腱形态的影响。

方法/设计:本研究设计为一项多中心、平行组RCT,采用均衡随机化(1:1)和盲法结局评估(证据等级:II),并将按照CONSORT声明进行报告。将通过门诊和广告招募50例在术后12 - 24个月存在双侧膝关节屈肌力量不对称的ACL重建患者(腘绳肌自体移植物)。患者将被随机分为一个为期12周的渐进性、力量和神经肌肉锻炼组(SNG),每周接受两次有监督的训练,或一个由家庭低强度锻炼计划组成的对照干预组(CON)。结局指标包括组间最大等长膝关节屈肌力量(主要结局)和膝关节伸肌力量的变化、手术侧腿的腘绳肌与股四头肌力量比以及膝关节损伤和骨关节炎结局评分(KOOS)(次要结局)。此外,还将研究几个探索性结局:国际膝关节文献委员会主观膝关节表格(IKDC)、Tegner活动评分、膝关节屈肌和伸肌的力量发展速率(RFD)、通过磁共振成像(MRI)评估的移植部位的肌腱再生和潜在肌肉肥大、姿势控制、动力学/运动学步态特征以及膝关节相关功能能力。

讨论

本RCT旨在研究ACL重建术后康复后期联合、渐进性抗阻和神经肌肉锻炼对膝关节屈肌/伸肌力量的影响。腘绳肌力量降低是继发性ACL断裂和骨关节炎加速进展的潜在危险因素。如果被证明有效,本研究中引入的干预模式可能有助于改善ACL重建患者的当前治疗策略。

试验注册

ClinicalTrials.gov,ID:NCT02939677(招募中)。于2016年10月20日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af4c/5787267/204ad79d6c2b/13063_2018_2448_Fig1_HTML.jpg

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