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临床试验/NCT06783062
NCT06783062尚未招募不适用

Activation Failure of Knee Extensors After Anterior Cruciate Ligament Rupture Depending on the Contraction Mode

La Tour Hospital0 个研究点目标入组 60 人开始时间: 2025年2月最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
主要终点
Voluntary Activation Level

研究概览

简要总结

The primary objective of the study is to evaluate the impact of ACL injury and ACL reconstruction on voluntary activation during maximal voluntary contraction (measured by neurophysiological parameters) according to the contraction mode.

The goal is to provide elements of knowledge to clinicians about the mechanisms of the activation failure depending on contraction mode, but also the resulting adapted clinical recommendations for conducting rehabilitation, and particularly for the use of different contraction modes.

The main hypothesis is that activation failure is not equal according to the contraction mode during maximal voluntary contractions and neurophysiological parameters will be decreased in comparison with non-injured subjects.

Secondary objectives are:

  • To analyze the evolution of neurophysiological parameters between sessions interspaced by several months according to the contraction mode.
  • To observe this time evolution depending on the treatment strategy chosen: rehabilitation or surgery plus rehabilitation.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • A. ACL-injured groups (surgically or conservatively treated):
  • Age between 18 and 50 years
  • Free, informed consent signed by the participant and the investigator.
  • Session 1: Delay of 2 to 6 weeks after injury, with a quiet knee (range of motion 110- 0°, minimal effusion, maximal contraction pain ≤ 2/10)
  • Session 2: Duration of 36 to 42 weeks after injury, with a quiet knee (range of motion 110-0°, minimal effusion, maximal contraction pain ≤ 2/10)
  • Independent person (Unprotected: under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision)
  • B. ControlGroup:
  • Age between 18 and 50 years
  • Free, informed consent signed by the participant and the investigator.
  • Sport practitioners: at least once per week practicing activities like collective sports, racket sports, combat sports, skiing, or on-loading activities with changing of directions.
  • Independent person (Unprotected: under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision)

排除标准

  • Subjects fitted with an implanted electronic device such as a cardiac pacemaker
  • Professional athlete
  • Pregnant women
  • Subject with systemic pathology or treatment affecting the musculoskeletal system
  • Subject with a history of neurological pathology or traumatic pathology, or pathology that required orthopedic treatment and/or surgery of the knee, hip and/or lumbar spine
  • Contraindication to isokinetic testing: incapacitating pain, evolving pathological process, non- healed fracture, unbalanced cardiovascular pathology (angina pectoris, arterial hypertension)
  • Contralateral knee injury
  • Subject inability to follow procedures or insufficient knowledge of project language
  • Data acquisition issue or injury during testing

结局指标

主要结局

Voluntary Activation Level

时间窗: Between 2 and 6 weeks after ACL rupture

次要结局

  • Maximal voluntary torque(Around 9 months after ACL rupture)
  • EMG activity of vastus lateralis, vastus medialis and rectus femoris(Around 9 months after ACL rupture)
  • Voluntary Activation Level(Around 9 months after ACL rupture)

研究者

发起方
La Tour Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Simon Barrué-Belou

Physiotherapist PhD., in charge of Biomechanics

La Tour Hospital

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