前交叉韧带重建后深蹲视觉生物反馈程序的疗效:一项前瞻性、平行、随机对照试验方案。

IF 2.1 Q3 SPORT SCIENCES
International Journal of Sports Physical Therapy Pub Date : 2025-09-02 eCollection Date: 2025-01-01 DOI:10.26603/001c.142879
Michael J Wellsandt, Neal Weldon, Dave M Werner, Matthew L McManigal, Matthew A Tao, Michael D Rosenthal, Balasrinivasa R Sajja, Christopher S Wichman, Ashley Baker, Christopher Johnson, Zachary Specht, Brittany A Weaver, Brian Knarr, Caleb Nabower, Elizabeth Wellsandt
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引用次数: 0

摘要

背景:前交叉韧带重建(ACLR)后,膝关节负荷的改变是普遍和持续的,是膝骨关节炎(OA)发展的重要驱动因素。目的:描述一项前瞻性、平行、随机对照试验,旨在评估ACLR术后早期实施的8周深蹲视觉生物反馈方案的疗效。研究设计:随机对照临床试验。方法:招募34例(13-35岁)进行前瞻性、平行、随机对照试验。在渐进式的、基于标准的术后物理治疗中,参与者将被随机分配到一个8周的体重深蹲项目中,其中有或没有视觉生物反馈,当治疗外科医生允许50%的负重时开始。结果将在干预前后、aclr后6个月和aclr后9个月进行测量。主要观察结果为:1)干预后深蹲时膝关节屈曲力矩脉冲肢间比的变化;2)干预前至6个月期间软骨微结构的变化。次要结局包括:1)aclr后6个月深蹲时膝关节屈曲力矩脉冲腿间比,2)干预后和aclr后6个月步态时膝关节屈曲力矩峰值腿间比,3)干预后和aclr后6个月股四头肌力量。探索性结果包括膝关节活动范围和积液、单腿跳跃测试、日常体力活动、额外的运动生物力学和患者报告的结果。讨论:本研究将评估ACLR术后早期实施的8周深蹲视觉生物反馈方案的效果。研究结果将为未来全面的膝关节负荷康复干预措施的开发和测试提供信息,这些干预措施旨在优化膝关节负荷的大小和频率,以预防前交叉韧带损伤后的早期膝关节OA。证据等级:NA。试验注册:Clinicaltrials.gov参考:NCT05363683。2022年5月6日注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficacy of a Squat Visual Biofeedback Program After ACL Reconstruction: Protocol for a Prospective, Parallel, Randomized Controlled Trial.

Efficacy of a Squat Visual Biofeedback Program After ACL Reconstruction: Protocol for a Prospective, Parallel, Randomized Controlled Trial.

Background: Altered knee joint loading is pervasive and persistent after anterior cruciate ligament reconstruction (ACLR) and a significant driver for the development of knee osteoarthritis (OA).

Purpose: To describe a prospective, parallel, randomized controlled trial aiming to evaluate the efficacy of an eight-week squat visual biofeedback program implemented early after ACLR.

Study design: Randomized controlled clinical trial.

Methods: Thirty-four individuals (13-35 years of age) will be recruited for a prospective, parallel, randomized controlled trial. Embedded within progressive, criterion-based post-operative physical therapy, participants will be randomly allocated to an eight-week bodyweight squatting program either with or without visual biofeedback initiated when 50% weightbearing is allowed by the treating surgeon. Outcomes will be measured at pre- and post-intervention, six months post-ACLR, and nine months post-ACLR. The primary outcomes are 1) change in knee flexion moment impulse interlimb ratio during squatting at post-intervention, and 2) change in cartilage microstructure from pre-intervention to six months. Secondary outcomes include 1) knee flexion moment impulse interlimb ratio during squatting at six months post-ACLR, 2) peak knee flexion moment interlimb ratio during gait at post-intervention and six months post-ACLR, and 3) quadriceps strength at post-intervention and six months post-ACLR. Exploratory outcomes include knee range of motion and effusion, single-legged hop tests, daily physical activity, additional movement biomechanics, and patient-reported outcomes.

Discussion: This study will assess the efficacy of an eight-week squat visual biofeedback program implemented early after ACLR. Findings will inform the future development and testing of comprehensive knee loading rehabilitation interventions that seek to optimize both the magnitude and frequency of knee joint loading to prevent early knee OA after ACL injuries.

Level of evidence: NA.

Trial registration: Clinicaltrials.gov reference: NCT05363683. Registered May 6, 2022.

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来源期刊
CiteScore
2.50
自引率
5.90%
发文量
124
审稿时长
16 weeks
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