Discipline of Podiatry, School of Allied Health, La Trobe University, Melbourne, Victoria, Australia.
La Trobe Sport and Exercise Medicine Research Centre, School of Allied Health, La Trobe University, Melbourne, Victoria, Australia.
Br J Sports Med. 2018 Mar;52(5):298-302. doi: 10.1136/bjsports-2017-098273. Epub 2017 Oct 22.
To evaluate the effectiveness of prefabricated foot orthoses for the prevention of lower limb overuse injuries in naval recruits.
This study was a participant-blinded and assessor-blinded, parallel-group randomised controlled trial. Three-hundred and six participants aged 17-50 years who undertook 11 weeks of initial defence training at the Royal Australian Navy Recruit School (Cerberus, Australia) were randomised to a control group (flat insoles, n=153) or an intervention group (contoured, prefabricated foot orthoses, n=153). The combined incidence of medial tibial stress syndrome, patellofemoral pain, Achilles tendinopathy and plantar fasciitis/plantar heel pain during the 11-week training period were compared using incidence rate ratios (IRR). Data were analysed using the intention-to-treat principle.
Sixty-seven injuries (21.9%) were recorded. The control and intervention group sustained 40 (26.1%) and 27 (17.6%) injuries, respectively (IRR 0.66, 95% CI 0.39 to 1.11, p=0.098). This corresponds to a 34% reduction in risk of developing medial tibial stress syndrome, patellofemoral pain, Achilles tendinopathy or plantar fasciitis/plantar heel for the intervention group compared with the control group. Participants in the prefabricated orthoses group were more likely to report at least one adverse event (20.3% vs 12.4%; relative risk (RR) 1.63, 95% CI 0.96 to 2.76; p=0.068; number needed to harm 13, 95% CI 6 to 253). The most common adverse events were foot blisters (n=20, 6.6%), arch pain (n=10, 3.3%) and shin pain (n=8, 2.6%).
Prefabricated foot orthoses may be beneficial for reducing the incidence of lower limb injury in naval recruits undertaking defence training.
Australian New Zealand Clinical Trials Registry: ACTRN12615000024549.
评估预制足部矫形器预防海军新兵下肢过度使用损伤的效果。
本研究是一项参与者盲法和评估者盲法的平行组随机对照试验。306 名年龄在 17-50 岁之间的参与者在澳大利亚皇家海军新兵学校(Cerberus)进行了 11 周的初始防御训练,他们被随机分为对照组(平足垫,n=153)或干预组(定制预制足部矫形器,n=153)。在 11 周的训练期间,使用发病率比值(IRR)比较内侧胫骨应力综合征、髌股疼痛、跟腱炎和足底筋膜炎/足底跟痛的综合发病率。使用意向治疗原则进行数据分析。
记录了 67 例损伤(21.9%)。对照组和干预组分别发生 40(26.1%)和 27(17.6%)例损伤(IRR 0.66,95%CI 0.39 至 1.11,p=0.098)。这意味着与对照组相比,干预组发生内侧胫骨应力综合征、髌股疼痛、跟腱炎或足底筋膜炎/足底跟痛的风险降低了 34%。预制矫形器组的参与者更有可能报告至少一种不良事件(20.3%比 12.4%;相对风险(RR)1.63,95%CI 0.96 至 2.76;p=0.068;需要伤害的人数 13,95%CI 6 至 253)。最常见的不良事件是足部水疱(n=20,6.6%)、足弓疼痛(n=10,3.3%)和胫骨疼痛(n=8,2.6%)。
预制足部矫形器可能有助于降低接受防御训练的海军新兵下肢损伤的发生率。
澳大利亚新西兰临床试验注册中心:ACTRN12615000024549。