跳至主要内容
临床试验/NCT06299943
NCT06299943Unknown不适用

Blind Randomized Controlled Study of Biofeedback Training Based on Target Biomechanical Gait Parameters at Patients in the Early Recovery Period of Stroke Whith Hemiparesis

Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health2 个研究点 分布在 2 个国家目标入组 120 人开始时间: 2022年1月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
120
试验地点
2
主要终点
Knee joint amplitude

研究概览

简要总结

Single-blinded controlled clinical trial. Biofeedback training courses based on target biomechanical gait parameters are being studied. For targeted biofeedback training, various biomechanical parameters are used: parameters of the gait cycle, EMG or kinematics of joint movements. The number of sessions is 8-11 for each patient. Clinical gain analysis is carried out before and after a course of training. Changes in biomechanical parameters that occurred at the end of the training course are assessed in comparison with those before training, and both statuses (before and after training) are compared with similar gait parameters in a group of healthy adults.

详细描述

Walking function disorders are typical for patients after cerebral stroke. A cerebral stroke normally affects one hemisphere and causes a hemiplegic syndrome. The gait of hemiplegic patients has very specific features: reduced walking speed, increased double stance phase, and reduced amplitude of movement in the leg joints. Biofeedback technology (BFB) is currently considered effective and promising for training walking function, including in patients after cerebral stroke. The technology is based on capturing a physiological parameter and presenting it to the patient in a perceivable form, so that the subject can understand its changes and respond appropriately. BFB can be used independently or as part of rehabilitation therapy. Nevertheless, efficiency, as noted by most authors, remains the subject of discussion. This is due to the fact, that at the previous stage of development of these systems, there was no technical capability to use the specific biomechanical gait parameters as targets for training. Therefore, more general parameters-such as walking speed, step frequency, etc.-were and are still used. This circumstance is attributable to the very nature of the main biomechanical gait parameters, which require special means of recording. One of the significant technical difficulties in BFB implementation is the need for accurate and fast registration of the gait parameters in real-time to use them for biofeedback. At the same time, the use of portable sensors for BFB training goals can represent a certain solution to technical problems. In recent years, owing to its important advantages, wearable IMU technology (systems using inertial measurement units) has been widely applied for capturing biomechanical gait parameters. Investigators used a system that was originally developed with our participation for targeted training based on biofeedback according to the biomechanical parameters of gait. The use of inertial technology and artificial intelligence technology has made it possible to use biomechanical parameters of gait (time and general gait parameters, EMG and kinematics of leg's joints) for biofeedback in a very low-cost and practically convenient way. Biofeedback training courses based on target biomechanical gait parameters are being studied. For targeted biofeedback training, various biomechanical parameters are used: parameters of the gait cycle, EMG or kinematics of joint movements. The number of sessions is 8-11 for each patient. Clinical gait analysis is carried out before and after a course of training. Changes in biomechanical parameters that occurred at the end of the training course are assessed in comparison with those before training, and both statuses (before and after training) are compared with similar gait parameters in a group of healthy adults.

Stroke patients participated in the study in Federal Center of Cerebrovascular Pathology and Stroke FMBA in Moscow, Russia. The study was approved by a local ethic committee and followed principles of the Declaration of Helsinki.

Single-blinded controlled clinical trial. The study involved stroke patients with hemiparesis (no more than 3 points on a scale Rankin). Experimental groups are determined by the target training parameter (time and general gait parameters, EMG and kinematics of leg's joints). One target parameter is using for one group. The number of sessions is 8-11 for each patient during three weeks of hospital stay. The duration of each session for each patient on each training day varies according to his well-being and current exercise tolerance, but does not exceed 30 minutes of training in one session. . Changes in biomechanical parameters that occurred at the end of the training course are assessed in comparison with those before training, and both statuses (before and after training) are compared with similar gait parameters in a group of healthy adults.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

Clinicians involved in the measurements and researchers that worked with data results did not know which group each patient was in.

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age - < 75 years;
  • type of stroke - ischemic;
  • structure of the lesion - cerebral hemisphere;
  • disease type - primary;
  • functional ability to walk for at least 5 minutes without using external means of support;
  • absence of reduced higher mental functions,
  • sensorimotor aphasia,
  • muscle tone in the limbs above 2 points according to Ashworth (Modified Ashworth Scale);
  • no history of orthopedic and neurological pathology; absence of pronounced pain syndrome

排除标准

  • Signs of orthostatic hypotension during training,
  • patient desire to withdraw from the study,
  • neurological deficit worsening.

研究组 & 干预措施

Target Biofeedbak gait training

Experimental

Patients in this group receive, in addition to conventional therapy, biofeedback gait training by selected biomechanical (Staince or single support phase, range of motion at joint or EMG amplitude) gait parameter. Training takes place 8-12 times over three weeks. The duration of each workout varies from 10 to 30 minutes.

干预措施: Biofeedback gait training by biomechanical target parameter (Other)

Target Biofeedbak gait training-2

Experimental

Patients in this group receive, in addition to conventional therapy, biofeedback gait training by selected biomechanical (Staince or single support phase, range of motion at joint or EMG amplitude) gait parameter. Training takes place 8-12 times over three weeks. The duration of each workout varies from 10 to 30 minutes.

干预措施: Biofeedback gait training by biomechanical target parameter (Other)

结局指标

主要结局

Knee joint amplitude

时间窗: Change from baseline at 3 weeks

knee joint range of motion at degree

EMG amplitude of quadriceps femoris muscle

时间窗: Change from baseline at 3 weeks

envelope EMG amplitude of the quadriceps femoris muscle at mkV

EMG amplitude of tibialis anterior muscle

时间窗: Change from baseline at 3 weeks

envelope EMG amplitude of the tibialis anterior muscle at mkV

Gait cycle

时间窗: Change from baseline at 3 weeks

gait cycle duration - at seconds;

Foot clearance

时间窗: Change from baseline at 3 weeks

foot clearance at centimeters;

Speed of walking

时间窗: Change from baseline at 3 weeks

walking speed - km/h;

EMG amplitude of gastrocnemus muscle

时间窗: Change from baseline at 3 weeks

envelope EMG amplitude of the gastrocnemus muscle at mkV

EMG amplitude of Hamstring muscle

时间窗: Change from baseline at 3 weeks

envelope EMG amplitude of the hamstring muscle at mkV

Stance phase

时间窗: Change from baseline at 3 weeks

stance phase at percent of gait cycle duration,

Single support phase

时间窗: Change from baseline at 3 weeks

single support phase at percent of gait cycle duration

Hip joint amplitude

时间窗: Change from baseline at 3 weeks

hip joint range of motion at degree

Ankle joint amplitude

时间窗: Change from baseline at 3 weeks

ankle joint range of motion at degree

次要结局

  • Activities of Daily Living(Change from baseline at 3 weeks)
  • Modified Rankin Scale for Neurologic Disability(Change from baseline at 3 weeks)
  • The Medical Research Council Weakness Scale(Change from baseline at 3 weeks)
  • Muscle strength(Change from baseline at 3 weeks)
  • The Timed Up and Go Test(Change from baseline at 3 weeks)

研究者

发起方
Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health
申办方类型
Other
责任方
Sponsor

研究点 (2)

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