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临床试验/NCT03239301
NCT03239301已完成不适用

Robotic-assisted Upper Extremity Training in Spinal Cord Injury Patients

Ankara Physical Medicine and Rehabilitation Education and Research Hospital4 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2017年8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
40
试验地点
4
主要终点
Spinal Cord Independence Measure III

研究概览

简要总结

Study design: Controlled Trial Objective: To evaluate the effectiveness of robotic-assisted training of forearm and hand functions in spinal cord injury patients Setting: Ankara Physical Medicine and Rehabilitation Training and Research Hospital, Turkey Methods: Forty patients were allocated into robotic and control groups. Both groups received conventional rehabilitation program for four weeks. Moreover, robotic group received robotic rehabilitation program tailored to the patient five times a week (each session of 30 min).

Baseline data and post-intervention data was compared.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

性别
All
接受健康志愿者

入选标准

  • Ages between 18-50
  • Cervical Level of Spinal Cord Injury

排除标准

  • Severe upper extremity contractures in the joints
  • Intensive spasticity (Ashworth 3-4)
  • Shoulder pain that causes exercise intolerance

研究组 & 干预措施

Conventional Rehabilitation

Active Comparator

Conventional rehabilitation program consisted range of motion (ROM) exercises, balance and coordination training, progressive resistive exercises, posture training, gait training, and occupational therapy as much as the patients tolerated. Conventional rehabilitation was tailored to the patient considering his requires and expectancies.

干预措施: Conventional Rehabilitation (Procedure)

Robotic Rehabilitation + Conventional Rehab

Active Comparator

The Armeo Spring HocomAG Inc. (Volketswil, Switzerland) device was used in robot assisted upper limb rehabilitation program. A

干预措施: Conventional Rehabilitation (Procedure)

Robotic Rehabilitation + Conventional Rehab

Active Comparator

The Armeo Spring HocomAG Inc. (Volketswil, Switzerland) device was used in robot assisted upper limb rehabilitation program. A

干预措施: Robotic REhabilitation (Procedure)

结局指标

主要结局

Spinal Cord Independence Measure III

时间窗: Four weeks

Scale Evaluating the Functionality and independence

Short Form-36

时间窗: Four weeks

Scale Evaluation the activities of daily living

Functional Independence Measure

时间窗: Four weeks

Scale Evaluating the Functionality

次要结局

未报告次要终点

研究者

发起方
Ankara Physical Medicine and Rehabilitation Education and Research Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Timur Ekiz

Medical Doctor, Physical and Rehabilitation Medicine Specialist

Ankara Physical Medicine and Rehabilitation Education and Research Hospital

研究点 (4)

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