Effects of Contralateral Strength Training on Postoperative Strength Deficits in the Immobilized Lower Extremity
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- KOOS
研究概览
简要总结
This is a prospective, randomized controlled trial that will enroll patients undergoing unilateral meniscal root repair or meniscus transplant. The objective of this study is to determine if immediate postoperative strength training of the contralateral (non-surgical) lower extremity reduces postoperative loss of strength in an immobilized lower extremity.
After the completion of surgery, patients will be randomized to either the experimental treatment (Group 1) or control group (Group II)for postoperative rehabilitation.
详细描述
Group I will receive knee flexion and extension strength training exercises for the contralateral (non-operative) lower extremity in addition to standard of care postoperative rehabilitation. The experimental strength training will be performed with moderate resistance and will require moderate effort. Exercises will include unilateral leg presses, lunges, step ups, and step downs. These exercises are performed as standard of care but are not typically introduced into the physical therapy regimen until 10-12 weeks postoperatively. In the experimental group, these exercises will be introduced starting with the first postoperative physical therapy session, but only for the contralateral (non-operative) leg.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 90 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient is indicated for meniscal root repair
- •Patient is indicated for meniscus transplant
- •Patient is at least 18 years of age
- •Patient is expected to survive at least 1 year beyond surgery
- •Patient has intact lower extremities bilaterally
- •Patient is willing to participate by complying with pre-and post-operative visit requirements
- •Patient is willing and able to review and sign a study informed consent form
排除标准
- •Lower extremity musculoskeletal defects
- •Systemic neuromuscular disorders
- •Failure to complete pre-operative BIDOEX strength assessment
- •Failure to complete pre-operative self-assessment score intake forms
结局指标
主要结局
KOOS
时间窗: 6 Weeks, 3 Months, 6 Months
A patient-reported outcome measurement instrument, developed to assess the patient's opinion about their knee and associated problems.
次要结局
未报告次要终点