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临床试验/NCT06699264
NCT06699264已完成不适用

Effekte Von Blood Flow Restriction Therapie Auf Das Schmerzempfinden Bei Patienten Mit Rekonstruktion Des Vorderen Kreuzbandes (Effects of Blood Flow Restriction Therapy on Pain Sensation in Patients With Anterior Cruciate Ligament Reconstruction)

Praxisklinik Rennbahn AG2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2023年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
2
主要终点
Rate of Pressure and Pain Treshold (Wagner FPX)

研究概览

简要总结

After surgical treatment of a tear of the anterior cruciate ligament, physiotherapeutic exercises are done as standard therapy. This is to achieve a rapid improvement in pain and knee function. In this study, the Investigators examine how low-intensity strength training with simultaneous restriction of blood flow works and whether it is effective and well tolerated. For this purpose, a pressure cuff is applied to the leg during training. Participation in this study will last four weeks for each participant. The Investigators will invite participants for 11 study visits. One appointment will last about 30 minutes. If a participant decides to take part in the study, they will be randomly assigned to one of two groups. The participants will belong to either an experimental group or the control group. In the experimental group, the participants will be treated with the intervention method. The intervention method involves 4 weeks of low-intensity strength training with an additional pressure cuff on the leg, which should lead to improved adaptations to the muscle as well as a reduction in pain. In the control group, the participants will receive the same strength training only without the additional pressure cuff. The benefit is that in addition to the participants actual rehabilitation program, each participant will receive free training to build their muscles. This could contribute to an accelerated rehabilitation process and a faster build-up of strength as well as an improvement in pain. It is additionally possible that the participants will help future patients with their participation. The intervention method for strength training with simultaneous restriction of blood flow (Blood Flow Restriction Training) has been studied for some time. There is good evidence of improved muscle, tendon and pain adaptations in both healthy individuals and patients with ACL injury. Whether this training method also has an effect on pain perception will be investigated in this study.

Participants may experience side effects if they are treated with the intervention method (low-intensity strength training with simultaneous restriction of blood flow). The Investigators may not yet know all the risks and side effects of the intervention method. So far, the following risks and side effects are known:

  • Temporay numbness
  • Muscle soreness
  • Pressure sensation

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 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • It must be your first anterior cruciate ligament surgery
  • You must be between 18 and 60 years old
  • You must be able to successfully complete certain exercises
  • The injury must have occurred no longer than 6 months ago

排除标准

  • Injury in other ligaments in the knee and cartilage
  • thrombosis
  • infection
  • high blood pressure (which is not treated with medication)

研究组 & 干预措施

Experimental Group

Experimental

Group 1 (experimental group) will be trained with the intervention method (low-load strength training) using the Tourniquet Touch (VBM Medizintechnik GmbH Einsteinstrasse 1, 72172 Sulz a.N., Germany)

干预措施: Blood Flow Restriction Training (Other)

Control Group

Active Comparator

Group 2 (controll group) receives the same strength training only without simultaneous restriction blood flow.

干预措施: Training without BFR (Other)

结局指标

主要结局

Rate of Pressure and Pain Treshold (Wagner FPX)

时间窗: Pre and post training as well as in week 1 of training

The Wagner FPX (Wagner Instruments, Greenwich, CT 06836-1217 USA) is used to quantify and document sensitivity and pain thresholds through defined application of pressure. Pain sensitivity is measured in kgf/s at four pre-defined positions: Position 1: dominant quadriceps muscles - centered on the muscle belly, 20 cm proximal to the proximal end of the patella Position 2: non-dominant quadriceps muscles - centered on the muscle belly, 20cm proximal to the proximal end of the patella Position 3: dominant m. biceps brachii - centered on the muscle belly, 10 cm proximal to the cubital fossa (= elbow bend) Position 4: non-dominant trapezius muscle (based on handedness) - centered on the muscle belly, 10 cm from the proximal end of the acromion in a direct line to the neck

Rate of Pressure and Pain Treshold (Wagner FPX)

时间窗: From enrollment to the end of training at 4 weeks as well as in week 1 of training

The Wagner FPX (Wagner Instruments, Greenwich, CT 06836-1217 USA) is used to quantify and document sensitivity and pain thresholds through defined application of pressure. Pain sensitivity is measured in kgf/s at four pre-defined positions: Position 1: dominant quadriceps muscles - centered on the muscle belly, 20 cm proximal to the proximal end of the patella Position 2: non-dominant quadriceps muscles - centered on the muscle belly, 20cm proximal to the proximal end of the patella Position 3: dominant m. biceps brachii - centered on the muscle belly, 10 cm proximal to the cubital fossa (= elbow bend) Position 4: non-dominant trapezius muscle (based on handedness) - centered on the muscle belly, 10 cm from the proximal end of the acromion in a direct line to the neck

Subjective Pain Measure (VAS score)

时间窗: From enrollment to the end of training at 4 weeks

As a subjective measure of knee joint pain, the perceived pain in the knee joint was further assessed using a visual analogue scale (VAS). The patients were asked to remember the most intense pain they experienced in their knee joint over the last week and rate it on the VAS. In order to evaluate a functional transfer of pain reduction, pain during a functional task (climbing stairs) was also assessed using VAS before and after the 4-week training intervention.

次要结局

  • Legpress 10-repition maximum voluntary contraction test (HUMAC NORM Isokinetic Dynamometer By CSMi)(pre and post training as well as in weeks 3 to 9)
  • Rate of muscle thickness of the m. rectus femoris in mm(Pre- and post training period)
  • Legpress 10-repition maximum voluntary contraction test (HUMAC NORM Isokinetic Dynamometer By CSMi)(From enrollment to the end of training at 4 weeks as well as in week 3 of training)
  • Rate of muscle thickness of the m. rectus femoris in mm(From enrollment to the end of training at 4 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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