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临床试验/NCT07454356
NCT07454356招募中不适用

Comparing High Intensity Stretch Device Combined With Physical Therapy Versus Physical Therapy Alone to Prevent Motion-Restoring Surgery Following Primary Total Knee Arthroplasty: Study Protocol for a Randomized Controlled Trial

Ermi LLC1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2025年12月9日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
150
试验地点
1
主要终点
Change from Enrollment in Active and Passive Knee Flexion Range of Motion (Degrees)

研究概览

简要总结

The goal of this clinical trial is to learn whether adding a stretching device to standard physical therapy can help people regain knee bending after total knee replacement surgery.

Some people have difficulty bending their knee during recovery. When this happens, doctors may recommend another procedure called motion-restoring surgery to improve knee movement.

This study aims to answer two main questions. First, does adding a hydraulic high-intensity stretching device to physical therapy help people regain knee bending after surgery? Second, does using the device affect recovery, daily activities, or the chance of needing another procedure?

Researchers will compare two treatment approaches. One group will receive standard physical therapy alone. The other group will receive standard physical therapy and will also use a hydraulic high-intensity stretching device called the Ermi Knee Flexionater at home.

Participants who receive the device will use it at home each day in addition to attending their physical therapy sessions. Researchers will measure how well participants can bend their knee and will ask questions about pain, daily function, and activity level. Participants will also complete simple walking and mobility tests.

Study visits will occur about four weeks after surgery when participants enroll, and again at about eight weeks, twelve weeks, six months, one year, and two years after surgery. Researchers will compare results between the two groups to see whether the stretching device improves recovery after knee replacement.

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
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 40 years or older
  • Undergoing primary total knee replacement surgery
  • Knee flexion less than 105 degrees at approximately 4 weeks after surgery
  • Considered a candidate for motion-restoring surgery, with any surgery delayed until after 2 months of nonoperative treatment

排除标准

  • Not willing to participate
  • Diagnosis of advanced rheumatoid arthritis
  • Neurological deficit affecting the operative leg
  • Revision total knee replacement or previous major surgery on the same knee
  • Cognitive impairment
  • Prior total hip replacement on the same side (ipsilateral total hip arthroplasty)
  • Living more than 2 hours from the study site or unwilling to attend required local physical therapy visits

研究组 & 干预措施

Physical Therapy Only

Active Comparator

Participants will receive standard postoperative physical therapy following primary total knee arthroplasty according to the treating clinician's usual rehabilitation protocol.

干预措施: Standard Physical Therapy (Other)

Hydraulic high-Intensity Stretch Device Plus Standard Physical Therapy

Experimental

Participants will receive standard postoperative physical therapy and will use a hydraulic high-intensity stretch device (Ermi Knee Flexionater) at home in accordance with the study protocol.

干预措施: Hydraulic high Intensity Stretch Device (Device)

结局指标

主要结局

Change from Enrollment in Active and Passive Knee Flexion Range of Motion (Degrees)

时间窗: Baseline (Enrollment at 4 weeks post-operative), 8 weeks post-operative, 12 weeks post-operative, 6 months post-operative, 1 year post-operative, and 2 years post-operative

Change in active and passive knee flexion measured in degrees using a standard goniometer. Higher values indicate greater knee flexion and improved range of motion.

次要结局

  • Change from Enrollment in KOOS Score(Baseline (Enrollment), 8 weeks, 12 weeks, 6 months, 1 year, and 2 years post-operative)
  • Change from Enrollment in WOMAC Score(Baseline (Enrollment), 8 weeks, 12 weeks, 6 months, 1 year, and 2 years post-operative)
  • Change from Enrollment in Visual Analog Scale (VAS) Pain Score(Baseline (Enrollment), 8 weeks, 12 weeks, 6 months, 1 year, and 2 years post-operative)
  • Change from Enrollment in Timed Up and Go (TUG) Test Time (Seconds)(Baseline (Enrollment), 8 weeks, 12 weeks, 6 months, 1 year, and 2 years post-operative)
  • Change from Enrollment in Six-Minute Walk Test (6MWT) Distance (Meters)(Baseline (Enrollment), 8 weeks, 12 weeks, 6 months, 1 year, and 2 years post-operative)
  • Number of Participants Experiencing Adverse Events(From enrollment to 2 years post-operative follow-up)

研究者

发起方
Ermi LLC
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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