Isokinetic Training With Blood Flow Restriction for Patellofemoral Pain Syndrome
2026年8月21日 更新者:Jingzhi Zhang、Nanjing Mingzhou Rehabilitation Hospital
Effects of Isokinetic Training Combined With Blood Flow Restriction in Patellofemoral Pain Syndrome
This randomized controlled trial aims to investigate the effects of isokinetic training combined with blood flow restriction (BFR) in individuals with patellofemoral pain syndrome (PFPS).
研究概览
地位
完全的
条件
研究类型
介入性
注册 (实际的)
60
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
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Nanjing、中国
- Nanjing Mingzhou Rehabilitation Hospital
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
接受健康志愿者
不
描述
Inclusion Criteria:
- Participants aged 18 to 40 years.
- Clinical diagnosis of patellofemoral pain syndrome (PFPS).
- Presence of anterior or retropatellar knee pain for at least 3 months.
- Pain provoked by at least two activities that increase patellofemoral joint load, including squatting, stair climbing, running, jumping, prolonged sitting, or kneeling.
- Average knee pain intensity of ≥3 on a 10-point visual analog scale (VAS) during aggravating activities.
- Ability to participate in exercise training and attend scheduled intervention sessions.
- Willingness to provide written informed consent.
Exclusion Criteria:
- History of knee surgery or significant trauma to the lower extremity within the previous 12 months.
- Clinical evidence of other knee disorders, including ligament injury, meniscal injury, patellar instability, osteoarthritis, or tendinopathy.
- Presence of neurological, cardiovascular, or systemic musculoskeletal disorders that may affect lower limb function or exercise participation.
- Current participation in other structured lower extremity rehabilitation or strength training programs.
- Contraindications to blood flow restriction training, including uncontrolled hypertension, vascular disease, thromboembolic disorders, or clotting abnormalities.
- Use of pain-relieving injections or surgical interventions for knee pain within the previous 6 months.
- Pregnancy.
- Inability to complete the assessment or intervention procedures.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:IT+BFR group
Isokinetic Training Combined With Blood Flow Restriction
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Participants in this group will receive isokinetic muscle strength training combined with blood flow restriction (BFR).
BFR will be applied to the proximal thigh using a pneumatic cuff at an individualized pressure based on limb occlusion pressure.
Isokinetic training will target the knee musculature using an isokinetic dynamometer under supervised conditions.
Each session will last 30 minutes, with training performed multiple times per week throughout the intervention period.
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有源比较器:IT group
Isokinetic Training
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Participants in this group will receive supervised isokinetic muscle strength training targeting the knee musculature using an isokinetic dynamometer.
Each session will last 30 minutes throughout the intervention period.
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有源比较器:ACE group
Aerobic Cycling Exercise
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Participants in this group will receive supervised aerobic cycling exercise using a stationary bicycle.
Training will be performed at a moderate intensity for 30 minutes per session throughout the intervention period.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Anterior Knee Pain Scale (AKPS)
大体时间:From enrollment to the end of treatment at 4 weeks
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The AKPS is a validated questionnaire used to assess pain and functional limitations associated with patellofemoral pain syndrome.
Scores range from 0 to 100, with higher scores indicating better knee function and fewer symptoms.
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From enrollment to the end of treatment at 4 weeks
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Zhang、Nanjing Mingzhou Rehabilitation Hospital
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2026年5月25日
初级完成 (实际的)
2026年8月15日
研究完成 (实际的)
2026年8月15日
研究注册日期
首次提交
2026年5月15日
首先提交符合 QC 标准的
2026年5月15日
首次发布 (实际的)
2026年5月22日
研究记录更新
最后更新发布 (实际的)
2026年8月25日
上次提交的符合 QC 标准的更新
2026年8月21日
最后验证
2026年8月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.