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临床试验/NCT05371444
NCT05371444已完成不适用

Effects of Control of Joint Degrees of Freedom in the Early Rehabilitation Post-stroke for the Recovery of Normal Movement (Non-compensatory) of the Upper Limb

University of Chile1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2021年4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
发起方
入组人数
45
试验地点
1
主要终点
Functioning Outcome 1

研究概览

简要总结

The study's methodology will be a single-blind, multicenter, parallel-group randomized controlled trial (RCT). The sample consists of stroke patients (supratentorial ischemic and hemorrhagic stroke of anterior territory) between 18 and 80 years of age, separated into 2 groups of 20 participants. The experimental group called "controlled DoF", the control group 1 called "non controlled DoF". The "controlled DoF" group will use an exoskeleton that will restrict the movement of the trunk and upper limb to release only the joint to work in the plane of interest. The "non-controlled DoF" group will receive the same therapy time as the previous group but without any restriction of joint movements. The training will be functional with multiarticular and combined planes tasks. All groups receive the conventional rehabilitation of the health center (ideally 45 minutes 1 per day). Using motion sensors, clinical scales, and electroencephalography (EEG), the data will be obtained pre-intervention, post-intervention, and in a follow-up at 3 and 6 months.

详细描述

This proposal seeks to demonstrate if the control of joint degrees of freedom (DoF) of the trunk and upper limb is determinant during the early rehabilitation phase post-stroke (here from day 1 to day 28 or first month) for the recovery of upper limb movements without compensations and the normal brain control (true recovery).

The study's methodology will be a single-blind, multicenter, parallel-group randomized controlled trial (RCT). The sample consists of stroke patients (supratentorial ischemic and hemorrhagic stroke of anterior territory) between 18 and 80 years of age, separated into 2 groups of 20 participants. The experimental group called "controlled DoF", the control group 1 called "non controlled DoF". The "controlled DoF" group will receive for the initial 2 weeks, 2 hours of therapy, 5 times a week (2 sessions of 1 hour per day, 5 days) and the next 2 weeks, 2 hours of therapy, 3 times a week(2 sessions of 1 hour of therapy, 3 days), using an exoskeleton that will restrict the movement of the trunk and upper limb to release only the joint to work in the plane of interest. The training will be selective in an articulation plane with the biofeedback of active movements (or active-assisted) employing a video game controlled by an external movement sensor installed in the segment of interest. The "non-controlled DoF" group will receive the same therapy time as the previous group but without any restriction of joint movements. The training will be functional with multiarticular and combined planes tasks. All groups receive the conventional rehabilitation of the health center (ideally 45 minutes 1 per day). Using motion sensors, clinical scales, and electroencephalography (EEG), the data will be obtained pre-intervention, post-intervention, and in a follow-up at 3 and 6 months.

The expected results would show more functional improvements with less compensatory kinematics for therapy that control DoF than for the therapy without control of the DoF or for conventional therapy in acute post-stroke patients. About this result, the EEG connectivity analysis would show a lower interhemispheric inhibition of the motor areas and a greater frontal-parietal flow during reaching and manipulation tasks in the group with DoF control.

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
Triple (Care Provider, Investigator, Outcomes Assessor)

盲法说明

The outcomes assessors will not now the arm to which each participant corresponds

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •(1) Clinical diagnosis of supratentorial ischemic stroke.
  • •(2) Time of onset <72 hours.
  • •(3) With alterations of the active voluntary movement of UL.
  • •(4) At least 3/8 DoF of the UE with MRC force scale of 3 or less.

排除标准

  • •(1) Cognitive impairment that prevents signing informed consent, following instructions and understanding procedures. (MoCA ≥ 18).
  • •(2) Musculoskeletal pathologies that prevent activities without pain or with limited ranges for the scope.
  • •(3) Severe visual impairment that does not allow the activities associated with the task.
  • •(4) Cerebellar o brainstem stroke.
  • •(5) Previous stroke leaving upper limb impairment.
  • •(6) Bilateral sensorimotor alterations.
  • •(7) Do not present alterations in functional clinical tests.

研究组 & 干预措施

Controlled DoF

Experimental

The treatment that this gruop will receive consist in a training with the exoskeleton that will restrict the DoF of the arm and trunk

干预措施: Training with restriction of the DoF (Behavioral)

Non controlled DoF

Active Comparator

The treatment that this gruop will receive consist in a training with out the exoskeleton and without restriction of the DoF

干预措施: Training without restriction of the DoF (Behavioral)

结局指标

主要结局

Functioning Outcome 1

时间窗: At week 1

Scale scores of Fugl Meyer Upper Limb test

Normal movements Outcome. Kinematics of grasping and reaching 4

时间窗: At week 24

Joint angles of the upper extremity in a glass test

Connectivity Outcome 1

时间窗: At week 1

Interhermispheric coherence of beta bands in the EEG.

Normal movements Outcome. Kinematics of grasping and reaching 1

时间窗: At week 1

Joint angles of the upper extremity in a water glass test

Normal movements Outcome. Kinematics of grasping and reaching 2

时间窗: At week 5

Joint angles of the upper extremity in a water glass test

Functioning Outcome 2

时间窗: At week 5

Scale scores of Fugl Meyer Upper Limb test

Normal movements Outcome. Kinematics of grasping and reaching 3

时间窗: At week 12

Joint angles of the upper extremity in a water glass test

Functioning Outcome 4

时间窗: At week 24

Scale scores of Fugl Meyer Upper Limb test

Functioning Outcome - function of the arm 3

时间窗: At week 12

Scale scores of ARAT (Action Research Arm Test)

Functioning Outcome - function of the arm 4

时间窗: At week 24

Scale scores of ARAT (Action Research Arm Test)

Functioning Outcome - quality of life 2

时间窗: At week 5

Scale scores of EQ-5D (quality of life test)

Functioning Outcome 3

时间窗: At week 12

Scale scores of Fugl Meyer Upper Limb test

Functioning Outcome - function of the arm1

时间窗: At week 1

Scale scores of ARAT (Action Research Arm Test)

Functioning Outcome - daily life activities 1

时间窗: At week 1

Scale scores of Barthel Index (independence in daily life activities)

Functioning Outcome - function of the arm 2

时间窗: At week 5

Scale scores of ARAT (Action Research Arm Test)

Functioning Outcome - daily life activities 2

时间窗: At week 5

Scale scores of Barthel Index (independence in daily life activities)

Functioning Outcome - daily life activities 3

时间窗: At week 12

Scale scores of Barthel Index (independence in daily life activities)

Connectivity Outcome 4

时间窗: At week 24

Interhermispheric coherence of beta bands in the EEG.

Functioning Outcome - daily life activities 4

时间窗: At week 24

Scale scores of Barthel Index (independence in daily life activities)

Functioning Outcome - quality of life 1

时间窗: At week 1

Scale scores of EQ-5D (quality of life test)

Functioning Outcome - quality of life 3

时间窗: At week 12

Scale scores of EQ-5D (quality of life test)

Functioning Outcome - quality of life 4

时间窗: At week 24

Scale scores of EQ-5D (quality of life test)

Connectivity Outcome 2

时间窗: At week 5

Interhermispheric coherence of beta bands in the EEG.

Connectivity Outcome 3

时间窗: At week 12

Interhermispheric coherence of beta bands in the EEG.

次要结局

未报告次要终点

研究者

发起方
University of Chile
申办方类型
Other
责任方
Principal Investigator
主要研究者

Pablo Burgos

Principal Investigator

University of Chile

研究点 (1)

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