Tamgüç Büşra, Pişirici Pelin
Bahcesehir University, Graduate Education Institute, Physiotherapy and Rehabilitation Doctoral Program, Istanbul, Turkiye.
Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Bahcesehir University, Istanbul, Turkiye.
Orthop J Sports Med. 2025 Apr 4;13(4):23259671251326454. doi: 10.1177/23259671251326454. eCollection 2025 Apr.
Current anterior cruciate ligament (ACL) injury prevention programs focus on integrating the athlete's cognitive and motor skills. A few studies examine the effectiveness of different types of attentional instructions on motor learning.
To investigate the acute and first-week effects of combined focus of attention and video instructions given to female athletes with dynamic knee valgus (DKV) and landing technique.
Controlled laboratory study.
A total of 30 athletes were randomized to (1) a verbal combined focus-instructed group (VFIG) (n = 10), (2) a video-instructed group (VIG) (n = 10), and (3) a control group (CG) (n = 10). DKV was assessed with frontal plane projection angle (FPPA) during the single-leg squat test, and landing technique was assessed with the Landing Error Scoring System (LESS) during drop vertical jump (DVJ) task. After pre-FPPA and pre-LESS values were recorded, 2 training blocks that contained 10 repetitions of the DVJ task in each were completed with group-specific instructions, and posttest measurements were taken immediately afterward and a week after as a retention test. Parametric tests were utilized due to the normal distribution of numerical descriptive features. Independent-sample tests compared numerical features between groups, chi-square tests assessed categorical features, and mixed-order analysis of variance evaluated variables based on retention times, with Bonferroni correction applied and a significance threshold set at < .05.
Statistical improvement occurred in both VFIG and VIG intragroup FPPA assessment at posttest and retention test (respectively, < .001; < .001; < .01). In the intergroup evaluation, FPPA showed superior improvement in VFIG at the posttest and retention test ( = .001; < .01). In the intragroup evaluation, there was a statistical improvement in LESS values in both VFIG and VIG, at the posttest and retention test (respectively, = .04; < .001; < .05), and VIG had superior improvement in the intragroup evaluation compared with VFIG. There was no statistically significant difference between LESS values in the intergroup evaluation (for all, > .05). There was no significant difference in the CG tests (for all, > .05).
Our study demonstrated that while both types of instructions were effective in improving knee valgus and landing technique, verbal combined focus instructions were superior in improving valgus. Future long-term studies will help in the understanding of the prevention of ACL injuries in female athletes.
Considering that female athletes have a higher risk of ACL injury due to higher DKV values than men, the authors believe that combined verbal and video instructions are important in reducing the knee valgus value and improving the landing technique, thus possibly reducing the injury rate.
NCT06424886 (ClinicalTrials.gov identifier).
当前的前交叉韧带(ACL)损伤预防方案侧重于整合运动员的认知和运动技能。一些研究探讨了不同类型的注意力指导对运动学习的有效性。
研究给予有动态膝外翻(DKV)和落地技术的女性运动员注意力集中与视频指导相结合的急性和第一周效果。
对照实验室研究。
总共30名运动员被随机分为(1)言语联合集中指导组(VFIG)(n = 10),(2)视频指导组(VIG)(n = 10),以及(3)对照组(CG)(n = 10)。在单腿深蹲测试期间,用额面投影角(FPPA)评估DKV,在垂直跳(DVJ)任务期间,用落地误差评分系统(LESS)评估落地技术。记录FPPA和LESS的预测试值后,完成2个训练组块,每个组块包含10次DVJ任务重复,并给予特定组别的指导,随后立即进行后测试测量,并在一周后作为保留测试进行测量。由于数值描述特征呈正态分布,因此采用参数检验。独立样本检验比较组间的数值特征,卡方检验评估分类特征,混合顺序方差分析根据保留时间评估变量,并应用Bonferroni校正,显著性阈值设定为P <.05。
在VFIG和VIG组内FPPA评估中,后测试和保留测试均出现统计学改善(分别为P <.001;P <.001;P <.01)。在组间评估中,FPPA在VFIG组的后测试和保留测试中显示出更好的改善(P =.001;P <.01)。在组内评估中,VFIG和VIG组的LESS值在测试后和保留测试中均有统计学改善(分别为P =.04;P <.001;P <.05),并且VIG在组内评估中的改善优于VFIG。组间评估中LESS值无统计学显著差异(所有P >.05)。CG测试无显著差异(所有P >.05)。
我们的研究表明,虽然两种类型的指导在改善膝外翻和落地技术方面均有效,但言语联合集中指导在改善外翻方面更优。未来的长期研究将有助于理解女性运动员ACL损伤的预防。
考虑到女性运动员由于DKV值高于男性而有更高的ACL损伤风险,作者认为言语和视频指导相结合对于降低膝外翻值和改善落地技术很重要,从而可能降低损伤率。
NCT06424886(ClinicalTrials.gov标识符)